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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Safety and pharmacodynamic effects of a pharmacological chaperone on α-galactosidase A activity and globotriaosylceramide clearance in Fabry disease: report from two phase 2 clinical studies</title><author><name sortKey="Germain, Dominique P" sort="Germain, Dominique P" uniqKey="Germain D" first="Dominique P" last="Germain">Dominique P. Germain</name><affiliation><nlm:aff id="I1">Division of Medical Genetics, Hôpital Raymond Poincaré (AP-HP), University of Versailles – St Quentin en Yvelines (UVSQ), Garches, 92380, France</nlm:aff></affiliation></author><author><name sortKey="Giugliani, Roberto" sort="Giugliani, Roberto" uniqKey="Giugliani R" first="Roberto" last="Giugliani">Roberto Giugliani</name><affiliation><nlm:aff id="I2">Medical Genetics Service, HCPA/UFRGS, Porto Alegre, Brazil</nlm:aff></affiliation></author><author><name sortKey="Hughes, Derralynn A" sort="Hughes, Derralynn A" uniqKey="Hughes D" first="Derralynn A" last="Hughes">Derralynn A. Hughes</name><affiliation><nlm:aff id="I3">Royal Free Campus, University College London, London, UK</nlm:aff></affiliation></author><author><name sortKey="Mehta, Atul" sort="Mehta, Atul" uniqKey="Mehta A" first="Atul" last="Mehta">Atul Mehta</name><affiliation><nlm:aff id="I3">Royal Free Campus, University College London, London, UK</nlm:aff></affiliation></author><author><name sortKey="Nicholls, Kathy" sort="Nicholls, Kathy" uniqKey="Nicholls K" first="Kathy" last="Nicholls">Kathy Nicholls</name><affiliation><nlm:aff id="I4">Royal Melbourne Hospital, Parkville, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Barisoni, Laura" sort="Barisoni, Laura" uniqKey="Barisoni L" first="Laura" last="Barisoni">Laura Barisoni</name><affiliation><nlm:aff id="I5">New York University School of Medicine, New York, NY, USA</nlm:aff></affiliation></author><author><name sortKey="Jennette, Charles J" sort="Jennette, Charles J" uniqKey="Jennette C" first="Charles J" last="Jennette">Charles J. Jennette</name><affiliation><nlm:aff id="I6">University of North Carolina, Chapel Hill, NC, USA</nlm:aff></affiliation></author><author><name sortKey="Bragat, Alexander" sort="Bragat, Alexander" uniqKey="Bragat A" first="Alexander" last="Bragat">Alexander Bragat</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Castelli, Jeff" sort="Castelli, Jeff" uniqKey="Castelli J" first="Jeff" last="Castelli">Jeff Castelli</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Sitaraman, Sheela" sort="Sitaraman, Sheela" uniqKey="Sitaraman S" first="Sheela" last="Sitaraman">Sheela Sitaraman</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Lockhart, David J" sort="Lockhart, David J" uniqKey="Lockhart D" first="David J" last="Lockhart">David J. Lockhart</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Boudes, Pol F" sort="Boudes, Pol F" uniqKey="Boudes P" first="Pol F" last="Boudes">Pol F. Boudes</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">23176611</idno><idno type="pmc">3527132</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527132</idno><idno type="RBID">PMC:3527132</idno><idno type="doi">10.1186/1750-1172-7-91</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">001657</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001657</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Safety and pharmacodynamic effects of a pharmacological chaperone on α-galactosidase A activity and globotriaosylceramide clearance in Fabry disease: report from two phase 2 clinical studies</title><author><name sortKey="Germain, Dominique P" sort="Germain, Dominique P" uniqKey="Germain D" first="Dominique P" last="Germain">Dominique P. Germain</name><affiliation><nlm:aff id="I1">Division of Medical Genetics, Hôpital Raymond Poincaré (AP-HP), University of Versailles – St Quentin en Yvelines (UVSQ), Garches, 92380, France</nlm:aff></affiliation></author><author><name sortKey="Giugliani, Roberto" sort="Giugliani, Roberto" uniqKey="Giugliani R" first="Roberto" last="Giugliani">Roberto Giugliani</name><affiliation><nlm:aff id="I2">Medical Genetics Service, HCPA/UFRGS, Porto Alegre, Brazil</nlm:aff></affiliation></author><author><name sortKey="Hughes, Derralynn A" sort="Hughes, Derralynn A" uniqKey="Hughes D" first="Derralynn A" last="Hughes">Derralynn A. Hughes</name><affiliation><nlm:aff id="I3">Royal Free Campus, University College London, London, UK</nlm:aff></affiliation></author><author><name sortKey="Mehta, Atul" sort="Mehta, Atul" uniqKey="Mehta A" first="Atul" last="Mehta">Atul Mehta</name><affiliation><nlm:aff id="I3">Royal Free Campus, University College London, London, UK</nlm:aff></affiliation></author><author><name sortKey="Nicholls, Kathy" sort="Nicholls, Kathy" uniqKey="Nicholls K" first="Kathy" last="Nicholls">Kathy Nicholls</name><affiliation><nlm:aff id="I4">Royal Melbourne Hospital, Parkville, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Barisoni, Laura" sort="Barisoni, Laura" uniqKey="Barisoni L" first="Laura" last="Barisoni">Laura Barisoni</name><affiliation><nlm:aff id="I5">New York University School of Medicine, New York, NY, USA</nlm:aff></affiliation></author><author><name sortKey="Jennette, Charles J" sort="Jennette, Charles J" uniqKey="Jennette C" first="Charles J" last="Jennette">Charles J. Jennette</name><affiliation><nlm:aff id="I6">University of North Carolina, Chapel Hill, NC, USA</nlm:aff></affiliation></author><author><name sortKey="Bragat, Alexander" sort="Bragat, Alexander" uniqKey="Bragat A" first="Alexander" last="Bragat">Alexander Bragat</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Castelli, Jeff" sort="Castelli, Jeff" uniqKey="Castelli J" first="Jeff" last="Castelli">Jeff Castelli</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Sitaraman, Sheela" sort="Sitaraman, Sheela" uniqKey="Sitaraman S" first="Sheela" last="Sitaraman">Sheela Sitaraman</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Lockhart, David J" sort="Lockhart, David J" uniqKey="Lockhart D" first="David J" last="Lockhart">David J. Lockhart</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author><author><name sortKey="Boudes, Pol F" sort="Boudes, Pol F" uniqKey="Boudes P" first="Pol F" last="Boudes">Pol F. Boudes</name><affiliation><nlm:aff id="I7">Amicus Therapeutics, Cranbury, NJ, USA</nlm:aff></affiliation></author></analytic><series><title level="j">Orphanet Journal of Rare Diseases</title><idno type="eISSN">1750-1172</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Fabry disease (FD) is a genetic disorder resulting from deficiency of the lysosomal enzyme α-galactosidase A (α-Gal A), which leads to globotriaosylceramide (GL-3) accumulation in multiple tissues. We report on the safety and pharmacodynamics of migalastat hydrochloride, an investigational pharmacological chaperone given orally at 150 mg every-other-day.</p></sec><sec><title>Methods</title><p>Two open-label uncontrolled phase 2 studies of 12 and 24 weeks (NCT00283959 and NCT00283933) in 9 males with FD were combined. At multiple time points, α-Gal A activity and GL-3 levels were quantified in blood cells, kidney and skin. GL-3 levels were also evaluated through skin and renal histology.</p></sec><sec><title>Results</title><p>Compared to baseline, increased α-Gal A activity of at least 50% was demonstrated in blood, skin and kidney in 6 of 9 patients. Patients’ increased α-Gal A activities paralleled the α-Gal A increases observed <italic>in vitro</italic> in HEK-293 cells transfected with the corresponding mutant form of the enzyme. The same 6 patients who demonstrated increases of α-Gal A activity also had GL-3 reduction in skin, urine and/or kidney, and had α-Gal A mutations that responded in transfected cells incubated with the drug. The 3 patients who did not show a consistent response <italic>in vivo</italic> had α-Gal A mutations that did not respond to migalastat HCl in transfected cells. Migalastat HCl was well tolerated.</p></sec><sec><title>Conclusions</title><p>Migalastat HCl is a candidate pharmacological chaperone that provides a novel genotype-specific treatment for FD. It enhanced α-Gal A activity and resulted in GL-3 substrate decrease in patients with responsive <italic>GLA</italic> mutations. Phase 3 studies are ongoing.</p></sec><sec><title>Trial registration</title><p>Clinicaltrial.gov: NCT00283959 and NCT00283933</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Germain, Dp" uniqKey="Germain D">DP Germain</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Eng, Cm" uniqKey="Eng C">CM Eng</name></author><author><name sortKey="Guffon, N" uniqKey="Guffon N">N Guffon</name></author><author><name sortKey="Wilcox, Wr" uniqKey="Wilcox W">WR Wilcox</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Schiffmann, R" uniqKey="Schiffmann R">R Schiffmann</name></author><author><name sortKey="Kopp, Jb" uniqKey="Kopp J">JB Kopp</name></author><author><name sortKey="Austin, Ha" uniqKey="Austin H">HA Austin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Alfhadel, M" uniqKey="Alfhadel M">M Alfhadel</name></author><author><name sortKey="Sirrs, S" uniqKey="Sirrs S">S Sirrs</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fan, Jq" uniqKey="Fan J">JQ Fan</name></author><author><name sortKey="Ishii, S" uniqKey="Ishii S">S Ishii</name></author><author><name sortKey="Asano, N" uniqKey="Asano N">N Asano</name></author><author><name sortKey="Suzuki, Y" uniqKey="Suzuki Y">Y Suzuki</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ishii, S" uniqKey="Ishii S">S Ishii</name></author><author><name sortKey="Chang, Hh" uniqKey="Chang H">HH Chang</name></author><author><name sortKey="Kawasaki, K" uniqKey="Kawasaki K">K Kawasaki</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Yam, Gh" uniqKey="Yam G">GH Yam</name></author><author><name sortKey="Zuber, C" uniqKey="Zuber C">C Zuber</name></author><author><name sortKey="Roth, J" uniqKey="Roth J">J Roth</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Benjamin, Er" uniqKey="Benjamin E">ER Benjamin</name></author><author><name sortKey="Flanagan, Jj" uniqKey="Flanagan J">JJ Flanagan</name></author><author><name sortKey="Schilling, A" uniqKey="Schilling A">A Schilling</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Khanna, R" uniqKey="Khanna R">R Khanna</name></author><author><name sortKey="Soska, R" uniqKey="Soska R">R Soska</name></author><author><name sortKey="Lun, Y" uniqKey="Lun Y">Y Lun</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Mayes, Js" uniqKey="Mayes J">JS Mayes</name></author><author><name sortKey="Scheerer, Jb" uniqKey="Scheerer J">JB Scheerer</name></author><author><name sortKey="Sifers, Rn" uniqKey="Sifers R">RN Sifers</name></author><author><name sortKey="Donaldson, Ml" uniqKey="Donaldson M">ML Donaldson</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wu, X" uniqKey="Wu X">X Wu</name></author><author><name sortKey="Katz, E" uniqKey="Katz E">E Katz</name></author><author><name sortKey="Della Valle, C" uniqKey="Della Valle C">C Della Valle</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Roddy, Tp" uniqKey="Roddy T">TP Roddy</name></author><author><name sortKey="Nelson, Bc" uniqKey="Nelson B">BC Nelson</name></author><author><name sortKey="Sung, Cc" uniqKey="Sung C">CC Sung</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fuller, M" uniqKey="Fuller M">M Fuller</name></author><author><name sortKey="Sharp, Pc" uniqKey="Sharp P">PC Sharp</name></author><author><name sortKey="Rozaklis, T" uniqKey="Rozaklis T">T Rozaklis</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Thurberg, Bl" uniqKey="Thurberg B">BL Thurberg</name></author><author><name sortKey="Rennke, H" uniqKey="Rennke H">H Rennke</name></author><author><name sortKey="Colvin, Rb" uniqKey="Colvin R">RB Colvin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Barisoni, L" uniqKey="Barisoni L">L Barisoni</name></author><author><name sortKey="Jennette, Jc" uniqKey="Jennette J">JC Jennette</name></author><author><name sortKey="Colvin, R" uniqKey="Colvin R">R Colvin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fan, Jq" uniqKey="Fan J">JQ Fan</name></author><author><name sortKey="Ishii, S" uniqKey="Ishii S">S Ishii</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Germain, Dp" uniqKey="Germain D">DP Germain</name></author><author><name sortKey="Fan, Jq" uniqKey="Fan J">JQ Fan</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Banikazemi, M" uniqKey="Banikazemi M">M Banikazemi</name></author><author><name sortKey="Bultas, J" uniqKey="Bultas J">J Bultas</name></author><author><name sortKey="Waldek, S" uniqKey="Waldek S">S Waldek</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kitagawa, T" uniqKey="Kitagawa T">T Kitagawa</name></author><author><name sortKey="Ishige, N" uniqKey="Ishige N">N Ishige</name></author><author><name sortKey="Suzuki, K" uniqKey="Suzuki K">K Suzuki</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Schiffmann, R" uniqKey="Schiffmann R">R Schiffmann</name></author><author><name sortKey="Waldek, S" uniqKey="Waldek S">S Waldek</name></author><author><name sortKey="Benigni, A" uniqKey="Benigni A">A Benigni</name></author><author><name sortKey="Auray Blais, C" uniqKey="Auray Blais C">C Auray-Blais</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Auray Blais, C" uniqKey="Auray Blais C">C Auray-Blais</name></author><author><name sortKey="Millington, Ds" uniqKey="Millington D">DS Millington</name></author><author><name sortKey="Barr, C" uniqKey="Barr C">C Barr</name></author><author><name sortKey="Young, Sp" uniqKey="Young S">SP Young</name></author><author><name sortKey="Mills, K" uniqKey="Mills K">K Mills</name></author><author><name sortKey="Clarke, Jt" uniqKey="Clarke J">JT Clarke</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Najafian, B" uniqKey="Najafian B">B Najafian</name></author><author><name sortKey="Svarstad, E" uniqKey="Svarstad E">E Svarstad</name></author><author><name sortKey="Bostad, L" uniqKey="Bostad L">L Bostad</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Whybra, C" uniqKey="Whybra C">C Whybra</name></author><author><name sortKey="Kampmann, C" uniqKey="Kampmann C">C Kampmann</name></author><author><name sortKey="Willers, I" uniqKey="Willers I">I Willers</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wilcox, Wr" uniqKey="Wilcox W">WR Wilcox</name></author><author><name sortKey="Oliveira, Jp" uniqKey="Oliveira J">JP Oliveira</name></author><author><name sortKey="Hopkin, Rj" uniqKey="Hopkin R">RJ Hopkin</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kuznetsov, G" uniqKey="Kuznetsov G">G Kuznetsov</name></author><author><name sortKey="Nigam, Sk" uniqKey="Nigam S">SK Nigam</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bradbury, J" uniqKey="Bradbury J">J Bradbury</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cohen, Fe" uniqKey="Cohen F">FE Cohen</name></author><author><name sortKey="Kelly, Jw" uniqKey="Kelly J">JW Kelly</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article" xml:lang="en"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Orphanet J Rare Dis</journal-id><journal-id journal-id-type="iso-abbrev">Orphanet J Rare Dis</journal-id><journal-title-group><journal-title>Orphanet Journal of Rare Diseases</journal-title></journal-title-group><issn pub-type="epub">1750-1172</issn><publisher><publisher-name>BioMed Central</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">23176611</article-id><article-id pub-id-type="pmc">3527132</article-id><article-id pub-id-type="publisher-id">1750-1172-7-91</article-id><article-id pub-id-type="doi">10.1186/1750-1172-7-91</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research</subject></subj-group></article-categories><title-group><article-title>Safety and pharmacodynamic effects of a pharmacological chaperone on α-galactosidase A activity and globotriaosylceramide clearance in Fabry disease: report from two phase 2 clinical studies</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" equal-contrib="yes" id="A1"><name><surname>Germain</surname><given-names>Dominique P</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>dominique.germain@rpc.aphp.fr</email></contrib><contrib contrib-type="author" equal-contrib="yes" id="A2"><name><surname>Giugliani</surname><given-names>Roberto</given-names></name><xref ref-type="aff" rid="I2">2</xref><email>rgiugliani@hcpa.ufrgs.br</email></contrib><contrib contrib-type="author" id="A3"><name><surname>Hughes</surname><given-names>Derralynn A</given-names></name><xref ref-type="aff" rid="I3">3</xref><email>rmgvdah@ucl.ac.uk</email></contrib><contrib contrib-type="author" id="A4"><name><surname>Mehta</surname><given-names>Atul</given-names></name><xref ref-type="aff" rid="I3">3</xref><email>atul.mehta1@nhs.net</email></contrib><contrib contrib-type="author" id="A5"><name><surname>Nicholls</surname><given-names>Kathy</given-names></name><xref ref-type="aff" rid="I4">4</xref><email>kathy.nicholls@mh.org.au</email></contrib><contrib contrib-type="author" id="A6"><name><surname>Barisoni</surname><given-names>Laura</given-names></name><xref ref-type="aff" rid="I5">5</xref><email>Laura.Barisoni@nyumc.org</email></contrib><contrib contrib-type="author" id="A7"><name><surname>Jennette</surname><given-names>Charles J</given-names></name><xref ref-type="aff" rid="I6">6</xref><email>charles_jennette@med.unc.edu</email></contrib><contrib contrib-type="author" id="A8"><name><surname>Bragat</surname><given-names>Alexander</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>abragat@amicusrx.com</email></contrib><contrib contrib-type="author" id="A9"><name><surname>Castelli</surname><given-names>Jeff</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>jcastelli@amicusrx.com</email></contrib><contrib contrib-type="author" id="A10"><name><surname>Sitaraman</surname><given-names>Sheela</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>ssitaraman@amicusrx.com</email></contrib><contrib contrib-type="author" id="A11"><name><surname>Lockhart</surname><given-names>David J</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>dlockhart@amicusrx.com</email></contrib><contrib contrib-type="author" id="A12"><name><surname>Boudes</surname><given-names>Pol F</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>pboudes@amicusrx.com</email></contrib></contrib-group><aff id="I1"><label>1</label>Division of Medical Genetics, Hôpital Raymond Poincaré (AP-HP), University of Versailles – St Quentin en Yvelines (UVSQ), Garches, 92380, France</aff><aff id="I2"><label>2</label>Medical Genetics Service, HCPA/UFRGS, Porto Alegre, Brazil</aff><aff id="I3"><label>3</label>Royal Free Campus, University College London, London, UK</aff><aff id="I4"><label>4</label>Royal Melbourne Hospital, Parkville, VIC, Australia</aff><aff id="I5"><label>5</label>New York University School of Medicine, New York, NY, USA</aff><aff id="I6"><label>6</label>University of North Carolina, Chapel Hill, NC, USA</aff><aff id="I7"><label>7</label>Amicus Therapeutics, Cranbury, NJ, USA</aff><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>24</day><month>11</month><year>2012</year></pub-date><volume>7</volume><fpage>91</fpage><lpage>91</lpage><history><date date-type="received"><day>8</day><month>7</month><year>2012</year></date><date date-type="accepted"><day>12</day><month>11</month><year>2012</year></date></history><permissions><copyright-statement>Copyright ©2012 Germain et al.; licensee BioMed Central Ltd.</copyright-statement><copyright-year>2012</copyright-year><copyright-holder>Germain et al.; licensee BioMed Central Ltd.</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><self-uri xlink:href="http://www.ojrd.com/content/7/1/91"></self-uri><abstract><sec><title>Background</title><p>Fabry disease (FD) is a genetic disorder resulting from deficiency of the lysosomal enzyme α-galactosidase A (α-Gal A), which leads to globotriaosylceramide (GL-3) accumulation in multiple tissues. We report on the safety and pharmacodynamics of migalastat hydrochloride, an investigational pharmacological chaperone given orally at 150 mg every-other-day.</p></sec><sec><title>Methods</title><p>Two open-label uncontrolled phase 2 studies of 12 and 24 weeks (NCT00283959 and NCT00283933) in 9 males with FD were combined. At multiple time points, α-Gal A activity and GL-3 levels were quantified in blood cells, kidney and skin. GL-3 levels were also evaluated through skin and renal histology.</p></sec><sec><title>Results</title><p>Compared to baseline, increased α-Gal A activity of at least 50% was demonstrated in blood, skin and kidney in 6 of 9 patients. Patients’ increased α-Gal A activities paralleled the α-Gal A increases observed <italic>in vitro</italic> in HEK-293 cells transfected with the corresponding mutant form of the enzyme. The same 6 patients who demonstrated increases of α-Gal A activity also had GL-3 reduction in skin, urine and/or kidney, and had α-Gal A mutations that responded in transfected cells incubated with the drug. The 3 patients who did not show a consistent response <italic>in vivo</italic> had α-Gal A mutations that did not respond to migalastat HCl in transfected cells. Migalastat HCl was well tolerated.</p></sec><sec><title>Conclusions</title><p>Migalastat HCl is a candidate pharmacological chaperone that provides a novel genotype-specific treatment for FD. It enhanced α-Gal A activity and resulted in GL-3 substrate decrease in patients with responsive <italic>GLA</italic> mutations. Phase 3 studies are ongoing.</p></sec><sec><title>Trial registration</title><p>Clinicaltrial.gov: NCT00283959 and NCT00283933</p></sec></abstract><kwd-group><kwd>Pharmacological chaperone</kwd><kwd>Conformational diseases</kwd><kwd>Protein-misfolding</kwd><kwd>Fabry disease</kwd><kwd>Lysosomal storage disorder</kwd></kwd-group></article-meta></front><body><sec><title>Background</title><p>Fabry disease (FD, OMIM 301500) is a rare, X-linked, multi-system genetic disorder [<xref ref-type="bibr" rid="B1">1</xref>]. Absent or deficient activity of lysosomal exoglycohydrolase α-galactosidase A (α-D-galactoside galactohydrolase, EC 3.2.1.22; α-Gal A) results in progressive accumulation of globotriaosylceramide (Gb<sub>3</sub> or GL-3) and related glycosphingolipids within lysosomes in a variety of cell types, including capillary endothelial cells, and renal (podocytes, tubular cells, glomerular endothelial, mesangial and intersticial cells), and nerve cells [<xref ref-type="bibr" rid="B1">1</xref>]. The primary disease process starts in infancy. With age, progressive damage to vital organ systems develops leading to organ failure. End-stage renal disease and life-threatening cardiovascular or cerebrovascular complications limit life-expectancy [<xref ref-type="bibr" rid="B1">1</xref>]. Treatment with life-long enzyme replacement therapy (ERT) infusions is available [<xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref>]. However, due to concerns regarding convenience, cost and incomplete effects on disease progression, unmet medical needs remain and other treatments are under investigation [<xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B4">4</xref>].</p><p>Studies of α-Gal A indicate that mutant forms of the enzyme are often retained in the endoplasmic reticulum (ER) and prematurely degraded because of reduced stability or improperly folded conformations [<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref>] as in other conformational or protein-misfolding diseases. This provides a rationale to use active site-specific pharmacological chaperones that bind and stabilize the nascent protein and restore efficient enzyme trafficking to lysosomes, the site of α-Gal A activity [<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B7">7</xref>]. Migalastat HCl (AT-1001, GR181413A, 1-deoxygalactonojirimycin) is a low molecular weight iminosugar that is orally bioavailable and that acts as a pharmacological chaperone for α-Gal A, targetting α-Gal A mutants that maintain catalytic competence [<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B8">8</xref>]. The mechanism of action of migalastat HCl is to bind and stabilize mutant α-Gal A initially in the ER, preventing misfolding and premature degradation and facilitating cellular trafficking to lysosomes where the breakdown of the GL-3 substrate can proceed [<xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B9">9</xref>].</p><p>We report on two phase 2 studies exploring the safety and pharmacodynamic responses to migalastat HCl in male patients with FD. In both studies, multiple parameters were evaluated to assess the effect of migalastat HCl on mutant α-Gal A activity and tissue GL-3.</p></sec><sec sec-type="methods"><title>Patients and methods</title><p>Two open-label, uncontrolled, phase 2 studies (FAB-CL-202, NCT00283959 and FAB-CL-203, NCT00283933, respectively) were conducted to evaluate the safety, tolerability, and pharmacodynamics of migalastat HCl in males with FD. Alpha-galactosidase A activity and GL-3 levels were evaluated in blood, urine, skin and kidney. Patients were treated with migalastat HCl 150 mg orally every other day for 12 weeks (FAB-CL-202) or 24 weeks (FAB-CL-203). Both studies incorporated a treatment extension for a total duration of 48 weeks. The studies received Ethical Committee/Institutional Review Board (IRB) approval and were conducted according to accepted standards of Good Clinical Practice (ICH-GCP) and in agreement with the Declaration of Helsinki.</p><p>Safety and pharmacodynamic data are presented for the first 12 to 24 weeks of initial treatment and, when available, include data from week-48 renal biopsies.</p><sec><title>Patients</title><p>Inclusion and exclusion criteria were similar for both studies. After written informed consent, male patients between 18 and 65 years of age with a confirmed diagnosis of FD were enrolled (Table <xref ref-type="table" rid="T1">1</xref>). A missense mutation in the <italic>GLA</italic> gene and residual α-Gal A activity of at least 3% of normal were required, as was the demonstration of an increase in α-Gal A activity in the presence of migalastat HCl in patient cultured lymphocytes. The initial criteria for enhancement required a relative increase in α-Gal A activity of at least 20% in the presence of 20 μM migalastat HCl. These criteria were later amended to a graded scale: if baseline activity was less than 1% of normal, it had to increase to at least 2% of normal; if activity was between 1% and 3% of normal, it had to at least double; if baseline activity was between 3% and 10%, it had to increase by at least 3% of normal; and if baseline activity was above 10%, it had to increase by at least 30%. Patients were to be naïve to ERT or willing to stop ERT for the duration of the study. Main exclusion criteria were significant disease or organ dysfunction, serum creatinine above 2 mg/dL and a QTc interval longer than 450 ms.</p><table-wrap position="float" id="T1"><label>Table 1</label><caption><p>Baseline characteristics</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th align="left"><bold>Patient ID</bold></th><th align="left"><bold>Age (years)</bold></th><th align="left"><bold>eGFR (mL/min/1.73 m</bold><sup><bold>2</bold></sup><bold>)</bold></th><th align="left"><bold>24-hour protein (mg)</bold></th><th align="left"><bold>Left Ventricle Mass (g)</bold></th><th align="left"><bold><italic>GLA </italic></bold><bold>mutation</bold></th><th align="left"><bold>HEK assay: amenable mutation?</bold></th></tr></thead><tbody valign="top"><tr><td align="left" valign="bottom">2-0102<hr></hr></td><td align="left" valign="bottom">27<hr></hr></td><td align="left" valign="bottom">143.8<hr></hr></td><td align="left" valign="bottom">270<hr></hr></td><td align="left" valign="bottom">138<hr></hr></td><td align="left" valign="bottom">p.L415P<hr></hr></td><td align="left" valign="bottom">NO<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0103<hr></hr></td><td align="left" valign="bottom">23<hr></hr></td><td align="left" valign="bottom">127.3<hr></hr></td><td align="left" valign="bottom">147<hr></hr></td><td align="left" valign="bottom">228<hr></hr></td><td align="left" valign="bottom">p.P259R<hr></hr></td><td align="left" valign="bottom">YES<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0104<hr></hr></td><td align="left" valign="bottom">18<hr></hr></td><td align="left" valign="bottom">156.1<hr></hr></td><td align="left" valign="bottom">131<hr></hr></td><td align="left" valign="bottom">123<hr></hr></td><td align="left" valign="bottom">p.P259R<hr></hr></td><td align="left" valign="bottom">YES<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0202<hr></hr></td><td align="left" valign="bottom">65<hr></hr></td><td align="left" valign="bottom">33<hr></hr></td><td align="left" valign="bottom">4640<hr></hr></td><td align="left" valign="bottom">312<hr></hr></td><td align="left" valign="bottom">p.R301Q<hr></hr></td><td align="left" valign="bottom">YES<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0301<hr></hr></td><td align="left" valign="bottom">39<hr></hr></td><td align="left" valign="bottom">121.1<hr></hr></td><td align="left" valign="bottom">--<sup>a</sup><hr></hr></td><td align="left" valign="bottom">225<hr></hr></td><td align="left" valign="bottom">p.F295C<hr></hr></td><td align="left" valign="bottom">YES <sup>b</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">3-0302<hr></hr></td><td align="left" valign="bottom">31<hr></hr></td><td align="left" valign="bottom">134.5<hr></hr></td><td align="left" valign="bottom">--<sup>a</sup><hr></hr></td><td align="left" valign="bottom">144<hr></hr></td><td align="left" valign="bottom">p.C94S<hr></hr></td><td align="left" valign="bottom">NO<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0303<hr></hr></td><td align="left" valign="bottom">36<hr></hr></td><td align="left" valign="bottom">90.3<hr></hr></td><td align="left" valign="bottom">--<sup>a</sup><hr></hr></td><td align="left" valign="bottom">175<hr></hr></td><td align="left" valign="bottom">p.R112C<hr></hr></td><td align="left" valign="bottom">NO<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF01<hr></hr></td><td align="left" valign="bottom">55<hr></hr></td><td align="left" valign="bottom">92.5<hr></hr></td><td align="left" valign="bottom"><100<hr></hr></td><td align="left" valign="bottom">231<hr></hr></td><td align="left" valign="bottom">p.N215S<hr></hr></td><td align="left" valign="bottom">YES<hr></hr></td></tr><tr><td align="left">3-RFO3</td><td align="left">47</td><td align="left">135.7</td><td align="left">150</td><td align="left">200</td><td align="left">p.P205T</td><td align="left">YES</td></tr></tbody></table><table-wrap-foot><p><sup>a</sup> Value not available.</p><p><sup>b</sup> Mutation was amenable only when higher doses of migalastat hydrochloride were used.</p></table-wrap-foot></table-wrap><p>The schedule of evaluation for α-Gal A activity and GL-3 parameters is shown in Table <xref ref-type="table" rid="T2">2</xref>. Skin biopsies and kidney biopsies were obtained at multiple time points.</p><table-wrap position="float" id="T2"><label>Table 2</label><caption><p>Schedule of evaluations for α-Gal A activity (lymphocytes, peripheral blood mononuclear cells, skin and kidney) and GL-3 (plasma, 24-hour urine, skin and kidney)</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th align="left"> </th><th align="left"><bold>Screening</bold></th><th align="left"><bold>Baseline</bold></th><th align="left"><bold>W4</bold></th><th align="left"><bold>W8</bold></th><th align="left"><bold>W12</bold></th><th align="left"><bold>W16</bold></th><th align="left"><bold>W20</bold></th><th align="left"><bold>W24</bold></th></tr></thead><tbody valign="top"><tr><td colspan="9" align="left" valign="bottom"><bold>α-Gal A activity</bold><hr></hr></td></tr><tr><td align="left" valign="bottom">Lymphocytes<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td></tr><tr><td align="left" valign="bottom">PBMCs<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">Skin<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">Kidney<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>d</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td colspan="9" align="left" valign="bottom"><bold>GL-3</bold><hr></hr></td></tr><tr><td align="left" valign="bottom">Plasma<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">Urine<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">Skin<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td></tr><tr><td align="left" valign="bottom">LC/MS<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">LM, EM<sup>a</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">LM Semi Q<sup>b</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">LM Quantitative<sup>c</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">Kidney<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td></tr><tr><td align="left" valign="bottom">LC/MS<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>d</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">LM, EM<sup>a</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>d</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">LM Semi Q<sup>b</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>d</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">+<sup>e</sup><hr></hr></td></tr><tr><td align="left">LM Quantitative<sup>c</sup></td><td align="left"> </td><td align="left">+</td><td align="left"> </td><td align="left"> </td><td align="left">+<sup>d</sup></td><td align="left"> </td><td align="left"> </td><td align="left">+<sup>e</sup></td></tr></tbody></table><table-wrap-foot><p>W = week, α-Gal A = alpha-galactosidase A, PBMCs = Peripheral Blood Mononuclear Cells, LC/MS = Liquid Chromatography/Mass Spectrometry, GL-3 = globotriaosylceramide, LM = Light Microscopy, EM = Electron Microscopy, Q = Quantitative.</p><p><sup>a</sup> Multiple cell types using a subjective scoring scale of 0, 1, 2, or 3 based on increasing GL-3 content.</p><p><sup>b</sup> Peritubular capillaries using a modified Thurberg’s method <sup>14</sup>.</p><p><sup>c</sup> Peritubular capillaries quantifying the number of GL-3 inclusion per cell using the the BLISS method <sup>15</sup>.</p><p><sup>d</sup> FAB CL-202 (NCT00283959) only.</p><p><sup>e</sup> FAB CL-203 (NCT00283933) only.</p></table-wrap-foot></table-wrap></sec><sec><title>Measurement of α-Gal A activity</title><p>At screening, patient lymphocytes were isolated from blood and cultured in media containing interleukin-2 and phytohemagglutin. Lymphocyte α-Gal A activity was measured in cell lysates with a fluorimetric assay using 4-methylumbelliferyl α-D-galactopyranoside as a substrate in the presence of galactosamine. Alpha-Gal A activities were measured alone and after 3 days of <italic>in vitro</italic> incubation with 20 μM migalastat HCl [<xref ref-type="bibr" rid="B10">10</xref>]. Fulfillment of the enhancement criteria was reported as Yes/No.</p><p>At screening and multiple time points during studies, peripheral blood mononuclear cells (PBMCs) were isolated and α-Gal A activity was measured using the previously described method [<xref ref-type="bibr" rid="B10">10</xref>] (MDS Pharmaceutical Services, Lincoln, NE). Values were normalized to measured total protein using a colorimetric assay and α-Gal A activity was reported as nmol/hour/mg protein. Results were obtained as absolute values and as a percentage of normal. The normal value was determined to be 22.0 +/− 5.7 nmol/hr/mg protein (mean +/− SD measured in 16 healthy volunteers in the migalastat HCl phase 1 study FAB-CL-102).</p><p>At baseline and during treatment skin and kidney biopsies were analyzed for α-Gal A activity in aqueous homogenates using a non-GLP method derived from the PBMC method (MDS, Montreal, Canada). Timing of samples is reported in Table <xref ref-type="table" rid="T2">2</xref>. Aqueous homogenization protocols for skin and kidney were developed and optimized for recovery of α-Gal A activity. Because enzyme activities may vary between tissues and even between cells within the same tissue, modifications were made to address technical issues associated with the limited amount of material and the potential for measured activities to be below the limit of detection in pre-treatment samples. Protocol modifications took into consideration the possibility for measured values to be above the level of detection but with insufficient sample volume to re-assay with dilution. The assay showed activity values varying by less than 10% in the kidney and by less than 20% in the skin. Control samples demonstrated good linearity over 50 serial 2-fold dilutions (average of <10% difference between predicted and measured signal). Measured values after 10-fold dilutions of the tissue samples were on average within 15% of predicted values for kidney, and within 25% of predicted values for skin.</p></sec><sec><title>Measurement of α-Gal A activity in HEK-293 cells</title><p>In parallel with these studies, efforts to better define the range of α-Gal A mutant forms that are amenable to migalastat HCl were implemented. An <italic>in vitro</italic> α-Gal A gene transfection assay, specific for each individual mutation, was developed in HEK-293 cells [<xref ref-type="bibr" rid="B11">11</xref>]. Criteria for response in the presence of 10 μM migalastat HCl were both an absolute increase of 3% of normal activity and a 20% relative increase [<xref ref-type="bibr" rid="B11">11</xref>]. The HEK-293 assay was retrospectively used to define if a patient carrying a GLA mutation was amenable to migalastat HCl.</p></sec><sec><title>Measurement of GL-3</title><sec><title>Plasma GL-3</title><p>Plasma GL-3 levels were measured at MDS Pharma (Lincoln, NE). An aliquot of human plasma (with EDTA) containing the analyte and internal standard was extracted using a precipitation procedure under UV-shielded conditions. The extracted samples were analyzed by high performance liquid chromatography (HPLC) coupled with an AB/MDS Sciex API 4000 mass spectrometer (MS). Using a closely related assay in 205 healthy volunteers, the mean (SD) normal value was estimated to be 3.5 (1.3) μg/mL [<xref ref-type="bibr" rid="B12">12</xref>].</p></sec><sec><title>Urine GL-3 (u-GL-3)</title><p>Whole urine GL-3 measurements on 24-hour samples were performed using LC-MS/MS analysis. Initially, determination was done at MDS Pharma Services (lower limit of detection 1 μg/mL). As most samples had levels of GL-3 that were below this limit of quantification, a more sensitive analysis was used. Samples were analyzed at the Department of Genetic Medicine, Women’s and Children’s Hospital, North Adelaide, Australia. Urine sediment was subjected to sonication to fragment cells. Urinary lipids from sediment and supernatant were extracted by liquid-liquid extraction. Following chromatography, GL-3 isoforms were detected by electrospray ionization tandem mass spectrometry in multi-reaction mode. Total GL-3 was reported as the sum of five isoforms (C16:0, C20:0, C22:0, C24:0, C24:1). The lower limit of detection was approximately 1 ng/mL. To correct for urinary sediment cell content, GL-3 was normalized to total phosphatidylcholine (PC) determined in the same LC-MS/MS assay. Results were expressed in pmol GL-3/nmol PC [<xref ref-type="bibr" rid="B13">13</xref>]. Urine GL-3 was also measured in samples from healthy volunteers. The mean (SD) urine GL-3 value in 29 healthy male volunteers was 48.6 (13.0) pmol GL-3/nmol PC. Subject values above 74.6 pmol total GL-3/nmol PC (mean + 2 SDs) were considered abnormal.</p></sec><sec><title>Skin and kidney GL-3</title><p>GL-3 was measured in skin and kidney tissues with LC-MS/MS under non-GLP conditions on aqueous samples derived from tissue homogenates (MDS Pharma Services, Montreal, Canada). The homogenization protocol was the same as for α-Gal A activity. After chromatography, GL-3 isoforms were detected using electrospray ionization tandem mass spectrometry in multi-reaction mode. The amount of GL-3 in the sample was reported as the sum of nine isoforms. Results were expressed as micrograms GL-3/g of tissue. The analytical range of the assay was 0.1 to 5.0 μg/g of tissue.</p></sec><sec><title>Skin and kidney histology</title><p>GL-3 accumulation was measured by histology in skin and kidney biopsies in multiple cell types. Analysis was performed using both light microscopy (LM) on glutaraldehyde-fixed and plastic-embedded sections stained with methylene blue-Azure II, and by electron microscopy (EM). Pathologists were blinded to the timing of the sample.</p><p>In skin and kidney, a GL-3 score was assigned by a single pathologist based on a semi-quantitative scale, with zero representing no GL-3 and three representing the most severe GL-3 accumulation [<xref ref-type="bibr" rid="B14">14</xref>]<sub>.</sub> In kidney, cells included podocytes, distal tubular cells and peri-tubular capillary endothelial cells (PTCs) [<xref ref-type="bibr" rid="B14">14</xref>]. For PTCs, the cell type previously used to determine the primary measure of efficacy for registration studies [<xref ref-type="bibr" rid="B14">14</xref>], the sensitivity of GL-3 analysis was further improved by using a novel scoring system, the Barisoni Lipid Inclusion Scoring System (BLISS) [<xref ref-type="bibr" rid="B15">15</xref>]. Two pathologists independently counted the total number of GL-3 inclusions per capillary in all 50–180 recorded capillaries and summarized the average score per PTC. The final BLISS score was the average of both pathologists’ scores.</p><p>Distal kidney tubules were also qualitatively evaluated for GL-3. Two pathologists individually determined whether there were fewer, equal, or more GL-3 inclusions present at the available time points.</p><p>A qualitative analysis of glomerular sclerosis was performed. For each available time point, two pathologists independently determined the percentage of glomeruli that were normal or sclerotic and further sub-categorized them as globally or segmentally sclerotic.</p><p>Finally, pharmacodynamic responses for α-Gal A activity and GL-3 were summarized for each patient to determine an overall individual response (post-hoc analysis). A positive response for α-Gal A activity was defined as an increase of at least 50% above baseline. Changes in GL-3 parameters were assessed as a percentage decrease from baseline of ≥ 20% for u-GL-3 and ≥50% in GL-3 inclusion number in PTCs. Evidence of an overall response was considered to be present if enhancement of α-Gal A activity was associated with GL-3 reduction in skin and/or kidney.</p></sec></sec><sec><title>Safety</title><p>Adverse events (AE), serious adverse events (SAE), laboratory (hematology, chemistry, and urinalysis) and patient drops-outs were evaluated all along the studies and extension periods.</p><p>When appropriate, descriptive statistics (mean, SD) were provided. Because of the small number of patients and the uncontrolled nature of the studies, no inferential statistics were used. Results are presented as individual patient data.</p></sec></sec><sec sec-type="results"><title>Results</title><p>Studies FAB CL-202 and FAB CL-203 recruited four and five subjects, respectively. The mean (SD) age at screening was 38 (15.4) years. The most frequent clinical manifestations at baseline were cold/heat intolerance (9/9), reduced sweating (9/9), angiokeratomas (8/9), acroparesthesias (7/9), hypoaccousia (5/9) and proteinuria (4/9). Three patients had hypertrophic cardiomyopathy. One patient had renal insufficiency (eGFR 33 mL/min/1.73 m<sup>2</sup>) (Table <xref ref-type="table" rid="T1">1</xref>).</p><p>All patients carried a missense mutant α-Gal A that was considered to be responsive in the initial lymphocyte assay. When subsequently tested in the HEK-293 transfection assay, only six patients had mutations considered amenable to migalastat HCl (p.P205T, p.N215S, p.P259R two patients, p.F295C, p.R301Q) while three had mutations that did not show a sufficient enzymatic activity increase in HEK-293 cells incubated with the drug (p.C94S, p.R112C, p.L415P) (Table <xref ref-type="table" rid="T1">1</xref>).</p><sec><title>Safety</title><p>Migalastat HCl was well tolerated. No subject discontinued treatment for an adverse event and there was no drop out for safety reasons. There were no deaths and no specific AE, serious adverse event (SAE), or laboratory abnormalities that were deemed related to migalastat HCl.</p></sec><sec><title>α-Gal A activity</title><p>At baseline, PBMC α-Gal A activity ranged from 0.05 to 6.11 nmol/hour/mg protein (Table <xref ref-type="table" rid="T3">3</xref>). The greatest activity corresponded to 16% of normal and in 8/9 subjects the activity was ≤ 1% of normal. During treatment, PBMC α-Gal A activity generally increased by the first time point and plateaued thereafter (Figure <xref ref-type="fig" rid="F1">1</xref>). For two subjects the maximum activity was seen at the last time point.</p><table-wrap position="float" id="T3"><label>Table 3</label><caption><p>α-Gal A activity in peripheral blood mononuclear cells (PBMCs, nmol/hr/mg protein)</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th align="left"> </th><th align="left"><bold>Screening</bold></th><th align="left"><bold>Baseline</bold></th><th align="left"><bold>Week 4</bold></th><th align="left"><bold>Week 8</bold></th><th align="left"><bold>Week 12</bold></th><th align="left"><bold>Week 16</bold></th><th align="left"><bold>Week 20</bold></th><th align="left"><bold>Week 24</bold></th></tr></thead><tbody valign="top"><tr><td colspan="9" align="left" valign="bottom">FAB CL-202 (NCT00283959) <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">2-0102<sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.15<hr></hr></td><td align="left" valign="bottom">0.14<hr></hr></td><td align="left" valign="bottom">0.14<hr></hr></td><td align="left" valign="bottom">0.18<hr></hr></td><td align="left" valign="bottom">0.12<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0103<hr></hr></td><td align="left" valign="bottom">0.22<hr></hr></td><td align="left" valign="bottom">0.24<hr></hr></td><td align="left" valign="bottom">2.23<hr></hr></td><td align="left" valign="bottom">1.76<hr></hr></td><td align="left" valign="bottom">2.3<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0104<hr></hr></td><td align="left" valign="bottom">0.5<hr></hr></td><td align="left" valign="bottom">0.21<hr></hr></td><td align="left" valign="bottom">2.88<hr></hr></td><td align="left" valign="bottom">3.18<hr></hr></td><td align="left" valign="bottom">3.36<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0202<hr></hr></td><td align="left" valign="bottom">0.5<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">7.53<hr></hr></td><td align="left" valign="bottom">6.45<hr></hr></td><td align="left" valign="bottom">7.12<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td colspan="9" align="left" valign="bottom">FAB CL-203 (NCT00283933) <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">3-0301<sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.13<hr></hr></td><td align="left" valign="bottom">0.08<hr></hr></td><td align="left" valign="bottom">0.17<hr></hr></td><td align="left" valign="bottom">0.17<hr></hr></td><td align="left" valign="bottom">0.22<hr></hr></td><td align="left" valign="bottom">0.19<hr></hr></td><td align="left" valign="bottom">0.25<hr></hr></td><td align="left" valign="bottom">0.36<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0302<hr></hr></td><td align="left" valign="bottom">0.18<hr></hr></td><td align="left" valign="bottom">0.10<hr></hr></td><td align="left" valign="bottom">0.08<hr></hr></td><td align="left" valign="bottom">0.07<hr></hr></td><td align="left" valign="bottom">BLQ<hr></hr></td><td align="left" valign="bottom">0.06<hr></hr></td><td align="left" valign="bottom">0.08<hr></hr></td><td align="left" valign="bottom">0.13<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0303<hr></hr></td><td align="left" valign="bottom">BLQ<hr></hr></td><td align="left" valign="bottom">0.14<hr></hr></td><td align="left" valign="bottom">0.36<hr></hr></td><td align="left" valign="bottom">0.37<hr></hr></td><td align="left" valign="bottom">BLQ<hr></hr></td><td align="left" valign="bottom">0.22<hr></hr></td><td align="left" valign="bottom">0.42<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF01<hr></hr></td><td align="left" valign="bottom">6.11<hr></hr></td><td align="left" valign="bottom">2.6<hr></hr></td><td align="left" valign="bottom">8.46<hr></hr></td><td align="left" valign="bottom">12.1<hr></hr></td><td align="left" valign="bottom">10.6<hr></hr></td><td align="left" valign="bottom">11.5<hr></hr></td><td align="left" valign="bottom">8.35<hr></hr></td><td align="left" valign="bottom">10.9<hr></hr></td></tr><tr><td align="left">3-RF03</td><td align="left">0.04</td><td align="left">0.2</td><td align="left">0.3</td><td align="left">0.57</td><td align="left">0.38</td><td align="left">0.51</td><td align="left">0.34</td><td align="left">1.32</td></tr></tbody></table><table-wrap-foot><p><sup>1</sup> Study number.</p><p><sup>2</sup> Patient ID.</p><p>BLQ = Below limit of quantification. Enzyme activity was reported as nmol/hour/mg protein.</p></table-wrap-foot></table-wrap><fig id="F1" position="float"><label>Figure 1</label><caption><p><bold>PBMC α-Gal A activity (as a percentage of normal) by week of migalastat HCl treatment.</bold> The red lines are for patients with mutations amenable to migalastat HCl as measured in the HEK-293 cell-based assay. The blue lines are for patients with non-responsive mutations. Values below 0.2 are below the limit of quantification (BLQ).</p></caption><graphic xlink:href="1750-1172-7-91-1"></graphic></fig><p>In skin homogenates, baseline α-Gal A activity ranged from 0.2 to 37.3 nmol/hour/mg protein. Following treatment, increases in α-Gal A activity of at least 50% were noted for all subjects (Table <xref ref-type="table" rid="T4">4</xref>).</p><table-wrap position="float" id="T4"><label>Table 4</label><caption><p>α-Gal A activity in skin and kidney (nmol 4-MU/hr/mg protein)</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th rowspan="2" align="left"> </th><th colspan="3" align="center" valign="bottom"><bold>Skin</bold><hr></hr></th><th colspan="3" align="center" valign="bottom"><bold>Kidney</bold><hr></hr></th></tr><tr><th align="left"><bold>Baseline</bold></th><th align="left"><bold>Week 12</bold></th><th align="left"><bold>Week 24</bold></th><th align="left"><bold>Baseline</bold></th><th align="left"><bold>Week 12</bold></th><th align="left"><bold>Week 24</bold></th></tr></thead><tbody valign="top"><tr><td colspan="7" align="left" valign="bottom">FAB CL-202 (NCT00283959) <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">2-0102 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.25<hr></hr></td><td align="left" valign="bottom">0.99<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">0.6<hr></hr></td><td align="left" valign="bottom">0.7<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0103 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.65<hr></hr></td><td align="left" valign="bottom">34.05<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">0.8<hr></hr></td><td align="left" valign="bottom">4.7<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0104 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">1.76<hr></hr></td><td align="left" valign="bottom">28.24<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">0.9<hr></hr></td><td align="left" valign="bottom">10.2<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0202 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">6.97<hr></hr></td><td align="left" valign="bottom">105<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">4.4<hr></hr></td><td align="left" valign="bottom">29.9<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td colspan="7" align="left" valign="bottom">FAB CL-203 (NCT00283933) <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">3-0301 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.92<hr></hr></td><td align="left" valign="bottom">3.08<hr></hr></td><td align="left" valign="bottom">2.6<hr></hr></td><td align="left" valign="bottom">0.4<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">1.2<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0302 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.37<hr></hr></td><td align="left" valign="bottom">2.36<hr></hr></td><td align="left" valign="bottom">1.13<hr></hr></td><td align="left" valign="bottom">1.7<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">1.3<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0303 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">0.82<hr></hr></td><td align="left" valign="bottom">2.97<hr></hr></td><td align="left" valign="bottom">1.37<hr></hr></td><td align="left" valign="bottom">0.8<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">1.0<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF01 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">37.29<hr></hr></td><td align="left" valign="bottom">139<hr></hr></td><td align="left" valign="bottom">133<hr></hr></td><td align="left" valign="bottom">21.6<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">157<hr></hr></td></tr><tr><td align="left">3-RF03 <sup>2</sup></td><td align="left">1.22</td><td align="left">22.77</td><td align="left">41.88</td><td align="left">1.5</td><td align="left">-</td><td align="left">14.7</td></tr></tbody></table><table-wrap-foot><p><sup>1</sup> Study number.</p><p><sup>2</sup> Patient ID.</p></table-wrap-foot></table-wrap><p>In kidney homogenates, α-Gal A activity at baseline ranged from 0.4 to 21.6 nmol/hour/mg protein. Following treatment, increases in α-Gal A activity of at least 50% were noted for 6/9 patients (Table <xref ref-type="table" rid="T4">4</xref>).</p></sec><sec><title>Plasma GL-3</title><p>At baseline, plasma GL-3 was between 1.12 and 4.82 μg/mL. No patient had values above normal. Week 12 data were not available for study FAB CL-202. One patient showed a transient increase of plasma GL-3, but otherwise there were no notable changes (data not shown).</p></sec><sec><title>Urine GL-3</title><p>All nine patients had elevated u-GL-3 prior to treatment; with a range from 170 to 3,876 pmol total GL-3/nmol PC. Compared to baseline, at the last time point decreased u-GL-3 levels of at least 20% were seen in 5/9 patients (Figure <xref ref-type="fig" rid="F2">2</xref>), all of whom had HEK-293 responsive mutations. Of the four patients without such a decrease, three had HEK-293 non-responsive mutations.</p><fig id="F2" position="float"><label>Figure 2</label><caption><p><bold>Total urine GL-3 (in pmol/nmol phosphotidlycholine) by week of migalastat HCl treatment.</bold> The red lines are for patients with an AT1001-amenable mutation in the HEK-293 cell-based assay, and the blue lines are for those with non-amenable mutations (Mutation p.F295C in patient 3–0301) was responsive only when high concentrations of migalastat HCl where used). Y axis: logarithmic scale.</p></caption><graphic xlink:href="1750-1172-7-91-2"></graphic></fig></sec><sec><title>Tissue GL-3 content</title><p>GL-3 in baseline renal biopsies ranged from 623 μg/g to 9,770 μg/g. During treatment GL-3 content decreased in five patients (4 of whom had HEK-293 responsive mutations) while 4 had an increase (Table <xref ref-type="table" rid="T5">5</xref>). Of these four, two had HEK-293 responsive mutations.</p><p>For skin, the baseline GL-3 content ranged from 6.7 μg/g to 360 μg/g. During treatment GL-3 content decreased in 3 patients, all of whom had HEK-293 responsive mutations (Table <xref ref-type="table" rid="T5">5</xref>).</p><table-wrap position="float" id="T5"><label>Table 5</label><caption><p>Skin and kidney GL-3 content at baseline, week 12 and week 24 (μg/g tissue)</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th rowspan="2" align="left"> </th><th colspan="2" align="center" valign="bottom"><bold>Baseline</bold><hr></hr></th><th colspan="2" align="center" valign="bottom"><bold>Week 12</bold><hr></hr></th><th colspan="2" align="center" valign="bottom"><bold>Week 24</bold><hr></hr></th></tr><tr><th align="left"><bold>Skin</bold></th><th align="left"><bold>Kidney</bold></th><th align="left"><bold>Skin</bold></th><th align="left"><bold>Kidney</bold></th><th align="left"><bold>Skin</bold></th><th align="left"><bold>Kidney</bold></th></tr></thead><tbody valign="top"><tr><td colspan="7" align="left" valign="bottom">FAB CL-202 <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">2-0102 <sup>2</sup><hr></hr></td><td align="left" valign="bottom">267<hr></hr></td><td align="left" valign="bottom">4170<hr></hr></td><td align="left" valign="bottom">269<hr></hr></td><td align="left" valign="bottom">3260<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0103<hr></hr></td><td align="left" valign="bottom">337<hr></hr></td><td align="left" valign="bottom">9510<hr></hr></td><td align="left" valign="bottom">233<hr></hr></td><td align="left" valign="bottom">5590<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0104<hr></hr></td><td align="left" valign="bottom">360<hr></hr></td><td align="left" valign="bottom">9770<hr></hr></td><td align="left" valign="bottom">309<hr></hr></td><td align="left" valign="bottom">9210<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0202<hr></hr></td><td align="left" valign="bottom">10.3<hr></hr></td><td align="left" valign="bottom">4140<hr></hr></td><td align="left" valign="bottom">11.2<hr></hr></td><td align="left" valign="bottom">3250<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td colspan="7" align="left" valign="bottom">FAB CL-203 <sup>1</sup><hr></hr></td></tr><tr><td align="left" valign="bottom">3-0301<sup>2</sup><hr></hr></td><td align="left" valign="bottom">223<hr></hr></td><td align="left" valign="bottom">3500<hr></hr></td><td align="left" valign="bottom">189<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">241<hr></hr></td><td align="left" valign="bottom">4960<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0302<hr></hr></td><td align="left" valign="bottom">230<hr></hr></td><td align="left" valign="bottom">2100<hr></hr></td><td align="left" valign="bottom">259<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">349<hr></hr></td><td align="left" valign="bottom">2860<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0303<hr></hr></td><td align="left" valign="bottom">246<hr></hr></td><td align="left" valign="bottom">623<hr></hr></td><td align="left" valign="bottom">344<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">300<hr></hr></td><td align="left" valign="bottom">2850<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF01<hr></hr></td><td align="left" valign="bottom">6.71<hr></hr></td><td align="left" valign="bottom">1340<hr></hr></td><td align="left" valign="bottom">9.38<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">10.3<hr></hr></td><td align="left" valign="bottom">4060<hr></hr></td></tr><tr><td align="left">3-RF03</td><td align="left">96.1</td><td align="left">5300</td><td align="left">64.8</td><td align="left">-</td><td align="left">41.5</td><td align="left">3390</td></tr></tbody></table><table-wrap-foot><p><sup>1</sup> Study number.</p><p><sup>2</sup> Subject number.</p></table-wrap-foot></table-wrap></sec><sec><title>GL-3 kidney histology</title><p>As LM and EM results were generally consistent, only LM results are presented.</p><p>On the semi-quantitative LM scale, podocytes had consistently more GL-3 than any of the other 12 renal cell types evaluated. Even when other cells had minimal or no inclusions (i.e., score of 0), podocytes always contained GL-3 inclusions. At baseline 9/9 patients had a podocyte score of 3 (maximum). The second most affected cells were the collecting tubular cells. However these cells were not always present on slides, making evaluation problematic. At baseline, 2/2 patients’ collecting duct cells had a GL-3 inclusion score of 3.</p><p>For PTCs, the semi-quantitative and quantitative (BLISS) results were generally similar both at baseline and during treatment (data not shown). The quantitative method however was more sensitive as it could score inclusions even if the semi-quantitative score was “0”. The quantitative results are presented in Table <xref ref-type="table" rid="T6">6</xref>. For 8/9 patients with available data, the baseline average count of GL-3 inclusions per cell ranged from 0.3 to 5.9. Between the first and last available biopsy the number of inclusions decreased in 4/8 patients, remained unchanged in 2/8, and increased in 2/8. Four of six patients who had HEK-293 responsive mutations had a score decrease, one had a score that did not change and one had a missing sample at baseline. Both patients who had an increase in score had mutations that were non-responsive in the HEK-293 assay. Of note, the inclusion count in PTCs did not always correlate with the changes in GL-3 on homogenized tissues.</p><table-wrap position="float" id="T6"><label>Table 6</label><caption><p>Quantitative GL3 scoring in kidney peri-tubular capillaries (PTC)</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th align="left"> </th><th align="left"><bold>Visit</bold></th><th align="left"><bold>Reader 1</bold></th><th align="left"><bold>Reader 2</bold></th><th align="left"><bold>Average</bold></th></tr></thead><tbody valign="top"><tr><td align="left" valign="bottom">FAB CL-202<sup>1</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td></tr><tr><td align="left" valign="bottom">2-0102<sup>2</sup><hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">2.3<hr></hr></td><td align="left" valign="bottom">2.3<hr></hr></td><td align="left" valign="bottom">2.3<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 12<hr></hr></td><td align="left" valign="bottom">5.7<hr></hr></td><td align="left" valign="bottom">6.6<hr></hr></td><td align="left" valign="bottom">6.2<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0103<hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">4.4<hr></hr></td><td align="left" valign="bottom">7.4<hr></hr></td><td align="left" valign="bottom">5.9<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 12<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0104<hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">2.3<hr></hr></td><td align="left" valign="bottom">3.5<hr></hr></td><td align="left" valign="bottom">2.9<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">0.9<hr></hr></td><td align="left" valign="bottom">1.4<hr></hr></td><td align="left" valign="bottom">1.2<hr></hr></td></tr><tr><td align="left" valign="bottom">2-0202<hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">0.5<hr></hr></td><td align="left" valign="bottom">0.2<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 12<hr></hr></td><td align="left" valign="bottom">0.8<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">0.5<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td></tr><tr><td align="left" valign="bottom">FAB CL-203<sup>1</sup><hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom"> <hr></hr></td></tr><tr><td align="left" valign="bottom">3-0301<sup>2</sup><hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">0.7<hr></hr></td><td align="left" valign="bottom">2.0<hr></hr></td><td align="left" valign="bottom">1.4<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 24<hr></hr></td><td align="left" valign="bottom">3.5<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">3.5<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">0<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">0<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0302<hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">2.4<hr></hr></td><td align="left" valign="bottom">2.6<hr></hr></td><td align="left" valign="bottom">2.6<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 24<hr></hr></td><td align="left" valign="bottom">3.5<hr></hr></td><td align="left" valign="bottom">5.4<hr></hr></td><td align="left" valign="bottom">4.5<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">4.4<hr></hr></td><td align="left" valign="bottom">4.2<hr></hr></td><td align="left" valign="bottom">4.3<hr></hr></td></tr><tr><td align="left" valign="bottom">3-0303<hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">3.5<hr></hr></td><td align="left" valign="bottom">2.2<hr></hr></td><td align="left" valign="bottom">2.9<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 24<hr></hr></td><td align="left" valign="bottom">1.0<hr></hr></td><td align="left" valign="bottom">1.2<hr></hr></td><td align="left" valign="bottom">1.1<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">2.6<hr></hr></td><td align="left" valign="bottom">3<hr></hr></td><td align="left" valign="bottom">2.8<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF01<sup>3</sup><hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">0.4<hr></hr></td><td align="left" valign="bottom">0.1<hr></hr></td><td align="left" valign="bottom">0.3<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 24<hr></hr></td><td align="left" valign="bottom">0.1<hr></hr></td><td align="left" valign="bottom">0.0<hr></hr></td><td align="left" valign="bottom">0.1<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 48<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">3-RF03<sup>4</sup><hr></hr></td><td align="left" valign="bottom">Baseline<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom"> <hr></hr></td><td align="left" valign="bottom">Week 24<hr></hr></td><td align="left" valign="bottom">0.0<hr></hr></td><td align="left" valign="bottom">0.1<hr></hr></td><td align="left" valign="bottom">0.1<hr></hr></td></tr><tr><td align="left"> </td><td align="left">Week 48</td><td align="left">0.0</td><td align="left">0.0</td><td align="left">0.1</td></tr></tbody></table><table-wrap-foot><p><sup>1</sup> Study number.</p><p><sup>2</sup> Subject number.</p><p><sup>3</sup> Week 48 biopsy not evaluable.</p><p><sup>4</sup> Baseline biopsy not evaluable.</p><p>Average number of GL-3 inclusions per cell as measured in biopsy samples at different time points (BLISS).</p></table-wrap-foot></table-wrap><p>Due to the variations in the number of glomeruli between biopsies, the assessment of glomerular sclerosis change was challenging (data not shown). At baseline, glomerulosclerosis was absent in 8/9 patients and absent during the study. For the remaining patient (2–02) only 2 non-sclerotic glomeruli were available at baseline. For this patient, glomerulosclerosis was noted at week 12 but was less marked at week 48.</p></sec><sec><title>GL-3 skin histology</title><p>Only LM results are presented. Most patients had low scores (0 or 1) at baseline and GL-3 inclusions were mostly seen in capillaries (endothelial cells and pericytes), large vessels (endothelial cells and medial smooth muscle cells) or perineurium (data not shown).There was no correlation between the presence of angiokeratoma and GL-3 scores: two patients who had no GL-3 deposition had angiokeratomas. No skin cells were individually as severely and consistently affected as kidney podocytes and there was a large variability of cell scores between patients. At baseline, the only cells that had a score of 3 were the perineurium (4/7) and large vessel smooth muscle cells (2/7). Results were highly variable throughout the study (data not shown). For capillary endothelial cells, when comparison between baseline and week 12 and week 24 data was made, 2/9 had a decrease (both had mutations that were responsive in the HEK-293 assay), 3/9 an increase, 4/9 unchanged. The observed changes were all less than 1 scoring unit.</p></sec><sec><title>Composite outcome</title><p>Table <xref ref-type="table" rid="T7">7</xref> provides a summary of α-Gal A and GL-3 responses to migalastat HCl. Six out of nine patients had responses in both α-Gal A and GL-3 parameters in skin and/or kidney, and all six had α-Gal A mutations that were responsive in the HEK-293 assay. Both patients with the same mutation (p.P259R) had consistent positive responses. The three subjects who did not demonstrate a clinical response had mutations that were not responsive in the HEK-293 assay.</p><table-wrap position="float" id="T7"><label>Table 7</label><caption><p>Summary of α-Gal A increase and GL-3 reduction for each patient and combined score according to HEK-293 response status</p></caption><table frame="hsides" rules="groups" border="1"><colgroup><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col><col align="left"></col></colgroup><thead valign="top"><tr><th align="left"><bold>Patient</bold></th><th align="left"><bold>2-0103</bold></th><th align="left"><bold>2-0104</bold></th><th align="left"><bold>2-0202</bold></th><th align="left"><bold>3-0301</bold></th><th align="left"><bold>3RF01</bold></th><th align="left"><bold>3RF03</bold></th><th align="left"><bold>2-0102</bold></th><th align="left"><bold>3-0302</bold></th><th align="left"><bold>3-0303</bold></th></tr></thead><tbody valign="top"><tr><td align="left" valign="bottom">Mutation<hr></hr></td><td align="left" valign="bottom">p.P259R<hr></hr></td><td align="left" valign="bottom">p.P259R<hr></hr></td><td align="left" valign="bottom">p.R301Q<hr></hr></td><td align="left" valign="bottom">p.F295C<hr></hr></td><td align="left" valign="bottom">p.N215S<hr></hr></td><td align="left" valign="bottom">p.P205T<hr></hr></td><td align="left" valign="bottom">p.L415P<hr></hr></td><td align="left" valign="bottom">p.C94S<hr></hr></td><td align="left" valign="bottom">p.R112C<hr></hr></td></tr><tr><td align="left" valign="bottom">HEK-293<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">R<hr></hr></td><td align="left" valign="bottom">NR<hr></hr></td><td align="left" valign="bottom">NR<hr></hr></td><td align="left" valign="bottom">NR<hr></hr></td></tr><tr><td align="left" valign="bottom">α-Gal A PBMC (at least +50%)<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td></tr><tr><td align="left" valign="bottom">α-Gal A kidney (at least +50%)<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">α-Gal A skin (at least +50%)<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td></tr><tr><td align="left" valign="bottom">u-GL3<hr></hr></td><td align="left" valign="bottom">+ (−60%)<hr></hr></td><td align="left" valign="bottom">+ (−75%)<hr></hr></td><td align="left" valign="bottom">+ (−38%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">+ (−20%)<hr></hr></td><td align="left" valign="bottom">+ (−52%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">GL-3 skin LC/MS<hr></hr></td><td align="left" valign="bottom">+ (−31%)<hr></hr></td><td align="left" valign="bottom">+ (−11%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">+ (−57%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">GL-3 kidney LC/MS<hr></hr></td><td align="left" valign="bottom">+ (−41%)<hr></hr></td><td align="left" valign="bottom">+ (−6%)<hr></hr></td><td align="left" valign="bottom">+ (−21%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">+ (−36%)<hr></hr></td><td align="left" valign="bottom">+ (−22%)<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left" valign="bottom">GL-3 kidney Inclusion (−50%)<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom">+<hr></hr></td><td align="left" valign="bottom"><sup>a</sup><hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td><td align="left" valign="bottom">-<hr></hr></td></tr><tr><td align="left">Combined score</td><td align="left">+</td><td align="left">+</td><td align="left">+</td><td align="left">+</td><td align="left">+</td><td align="left">+</td><td align="left">-</td><td align="left">-</td><td align="left">-</td></tr></tbody></table><table-wrap-foot><p>HEK-293 = transfection assay in Human Embryonic Kidney-293 cells, R = responsive mutation, NR = non-responsive mutation, α-Gal A = alpha galactosidase A, PBMCs = Peripheral Blood Mononuclear Cells, GL-3 = globotriaosylceramide, u = urine, s = skin, k = kidney, LC/MS = Liquid Chromatography - Mass Spectrometry.</p><p><sup>a</sup> baseline biopsy not evaluable.</p></table-wrap-foot></table-wrap></sec></sec><sec sec-type="discussion"><title>Discussion</title><p>Mutations in proteins that reduce stability or lead to protein misfolding are common causes of lysosomal storage diseases. Unstable or misfolded mutant enzymes are recognized by the cellular endoplasmic reticulum (ER) quality control system and prematurely degraded before reaching lysosomes. Some iminosugars have a high affinity for the active site of lysosomal enzymes, and can reversibly bind, stabilize and act as specific pharmacological chaperones [<xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B16">16</xref>,<xref ref-type="bibr" rid="B17">17</xref>]. Stabilized mutant can pass ER quality control more efficiently and traffic to lysosomes [<xref ref-type="bibr" rid="B7">7</xref>]. Once in lysosomes, the non-covalently bound chaperones can dissociate, freeing the enzyme to bind its substrate [<xref ref-type="bibr" rid="B5">5</xref>].</p><p>In FD, this approach was first demonstrated in patients’ lymphoblasts using 1-deoxygalactonojirimycin (migalastat HCl) [<xref ref-type="bibr" rid="B5">5</xref>]. Migalastat HCl mimics the terminal α-galactose of GL-3 and binds to the active site of α-Gal A with high affinity and specificity [<xref ref-type="bibr" rid="B6">6</xref>]. The binding increases the stability of the enzyme, shifts the folding in favor of the proper conformation and allows traffic to lysosomes [<xref ref-type="bibr" rid="B17">17</xref>].</p><p>The objectives of the current studies were to explore the safety and pharmacodynamics of migalastat HCl in 9 male FD patients given 150 mg orally every other day.</p><p>Results from a 12-week and a 24-week study with similar design were combined. There was a consistent increase in α-Gal A activity in PBMCs, skin and kidney in patients carrying responsive <italic>GLA</italic> mutations. In PBMCs, increases were rapid (week 4) and sustained over the duration of treatment. One patient, with a low baseline α-Gal A activity, showed a progressive increase with a maximum only reached at week 24. Some patients reached an enzyme activity in PBMCs of 30% to 50% of normal. Increase in α-Gal A activity were associated with substrate reduction, as demonstrated by a decrease in urinary GL-3 and GL-3 inclusions in renal PTCs.</p><p>These results indicate that the activity of mutated α-Gal A can be increased <italic>in vivo</italic> following administration of migalastat HCl. The binding of the drug to α-Gal A is reversible and is of lower affinity in the acidic environment of the lysosome. Furthermore, migalastat HCl is rapidly cleared from plasma (half-life 3–4 hours), whereas the lysosomal half-life of the enzyme is significantly longer (around 110–120 hours) [<xref ref-type="bibr" rid="B8">8</xref>]. This allows the enzyme to bind and turn over the GL-3 substrate without inhibition by the small molecule. The every-other-day regimen allows additional time for the chaperone to dissociate from the enzyme.</p><p>The <italic>in vitro</italic> HEK-293 cell-based assay [<xref ref-type="bibr" rid="B11">11</xref>] appears to predict the clinical pharmacodynamic response. Of note, both patients with the same p.P259R mutation showed similar pharmacodynamic response. As these studies included only 9 patients carrying 8 different missense mutations, results should be interpreted with caution. The predictive value of the assay will have to be confirmed in larger numbers of FD patients with additional mutations. This assay is currently used to select patients for phase 3 clinical studies.</p><p>FD is a rare, lifelong devastating disease, punctuated by acute complications that take many clinical forms [<xref ref-type="bibr" rid="B1">1</xref>]. FD phenotypic expression varies from one patient to the next, even within families harboring the same genotype. It is thus a challenge to select clinical outcome measures that can consistently demonstrate therapeutic efficacy [<xref ref-type="bibr" rid="B18">18</xref>]. Because GL-3 is the primary lysosomal substrate of α-Gal A, the deficient enzyme in FD, demonstrating a decrease in GL-3 could reflect treatment efficacy.</p><p>While GL-3 deposition in renal PTCs has been used as the primary outcome measure of efficacy for the approval of agalsidase beta [<xref ref-type="bibr" rid="B2">2</xref>], this choice may not be appropriate. Despite an overt clinical expression of the disease, our patients had limited amounts of GL-3 in capillary cells of the kidney and skin, and normal levels of GL-3 in plasma. Kidney histology revealed that GL-3 deposition was extensive in podocytes and collecting duct cells, but minimal in PTCs. A previously used histological method for quantifying GL-3 in PTCs [<xref ref-type="bibr" rid="B14">14</xref>] was not sensitive enough to evaluate the low levels of inclusions observed. Thus, a more sensitive method to quantify GL-3 PTC inclusions was developed [<xref ref-type="bibr" rid="B15">15</xref>]. Interestingly, the shedding into the urinary tract of tubular cells, and potentially podocytes, accounts for most of the urinary GL-3 in FD [<xref ref-type="bibr" rid="B19">19</xref>]<sub>,</sub> especially when plasma GL-3 levels are low and glomerular filtration of GL-3 negligible. A decrease in u-GL-3 was observed in our subjects and has been advocated as a marker of efficacy in FD, however the clinical relevance remains controversial [<xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B20">20</xref>]. Some of the controversies stem from a lack of a reliable method for collection of samples and analysis [<xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B21">21</xref>]<sub>.</sub> To address these concerns, a new GLP assay for urine GL-3 was developed and validated, and will be used in ongoing migalastat HCl phase 3 studies.</p><p>In contrast to ERT, migalastat HCl is a small molecule that is excreted unchanged in the urine and can potentially reach podocytes. These cells are central to the renal pathophysiology of FD [<xref ref-type="bibr" rid="B22">22</xref>]. Migalastat HCl was generally well tolerated. However, these studies only enrolled 9 subjects and this should be interpreted with evident caution. Long-term extension data from phase 2 studies also indicate that the drug is well tolerated and, as of this writing, no severe adverse reactions related to treatment have been identified after four years of treatment.</p><p>A key issue for physicians treating FD patients is the selection of candidates for pharmacological chaperone therapy. Severe <italic>GLA</italic> defects that result in no residual α-Gal A activity are probably not addressable with chaperone therapy, and only patients who express missense mutants with low levels of activity were included. Different methods were explored to predict which patients would respond to migalastat HCl [<xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B11">11</xref>]. We initially recruited patients with missense mutations who had at least 3% of normal activity that increased by at least 20% when lymphocytes were incubated with migalastat HCl. However, the <italic>ex vivo</italic> lymphocyte assay is complex and cannot be readily performed under GLP conditions. Moreover, the lymphocyte assay did not always correlate with the <italic>in vivo</italic> PBMC assay. Ultimately, lymphocyte and PBMC assays are not useful in heterozygous FD females. In an X-linked disease, females are mosaics and isolated cells are a mix of cells with normal α-Gal A and ones with mutated α-Gal A. In females, an increase in activity with migalastat HCl might reflect the chaperoning of the wild-type enzyme. It has been increasingly recognized that females with FD can have significant clinical manifestations [<xref ref-type="bibr" rid="B23">23</xref>,<xref ref-type="bibr" rid="B24">24</xref>]. For these reasons, an <italic>in vitro</italic> assay was developed that could be used irrespective of sex [<xref ref-type="bibr" rid="B11">11</xref>].</p><p>In summary, migalastat HCl is a candidate pharmacological chaperone that provides a genotype-specific treatment for FD. When administered at an oral dose of 150 mg on an every-other-day regimen, it was well tolerated, increased α-Gal A activity in patients with responsive <italic>GLA</italic> mutations, and resulted in GL-3 substrate reduction. Phase 3 studies of migalastat HCl for FD are ongoing.</p><p>This study describes the first use in patients of an oral small molecule pharmacological chaperone, rather than using enzyme replacement therapy, to treat a lysosomal storage disorder. It shows for the first time in medicine that such a drug increases the activity, or effectively rescues the mutated and dysfunctional enzyme that patients with Fabry disease have expressed their entire lives. In addition to being a novel approach for the treatment of Fabry disease, stabilization of target proteins using small cell-permeable pharmacological chaperones, may represent a generally applicable rescue strategy for other diseases that result from improper protein folding and inefficient cellular targeting [<xref ref-type="bibr" rid="B25">25</xref>-<xref ref-type="bibr" rid="B27">27</xref>].</p></sec><sec><title>Competing interests</title><p>DPG is an investigator for Amicus and has received research funding, consultancy fees, and travel expenses from Genzyme and Shire HGT. RG is a consultant and investigator for Actelion, Amicus, BioMarin, Genzyme and Shire HGT. DAH is a consultant for Amicus, Shire HGT, Genzyme, Actelion, has Speaker’s Bureau for Amicus, Shire HGT, Genzyme, and Actelion, and has received grants from Amicus, Shire HGT, and Genzyme. KN has received travel and research support and speaker's honoraria from Amicus, Shire HGT and Genzyme. AM has received honoraria, research funding, consultancy fees, and travel expenses from Shire HGT, Genzyme, Actelion, Protalix, and Amicus. AB, JC, SS, DJL and PFB are Amicus employees.</p></sec><sec><title>Authors’ contributions</title><p>DPG, RG, DAH, AM and KN performed all clinical investigations. LB and CJJ completed the kidney biopsies reading. AB, JC, SS and DJL designed and performed experiments. DPG and PFB analyzed and interpreted the data, and wrote the manuscript. All the authors discussed the results and commented on the manuscript at all stages. All the authors have read and approved the final manuscript.</p></sec></body><back><sec><title>Acknowledgements</title><p>We thank the patients and their families for their dedication and cooperation; Dr. Ron Gordon (Department of Pathology, Mount Sinai School of Medicine, NY, NY, USA), Pr. Albert A. 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