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Anti-MAdCAM-1 antibody (PF-00547659) for active refractory Crohn's disease in Japanese and Korean patients: the OPERA study.
Saruta, Masayuki; Park, Dong Il; Kim, Young-Ho; Yang, Suk-Kyun; Jang, Byung-Ik; Cheon, Jae Hee; Im, Jong Pil; Kanai, Takanori; Katsuno, Tatsuro; Ishiguro, Yoh; Nagaoka, Makoto; Isogawa, Naoki; Li, Yinhua; Banerjee, Anindita; Ahmad, Alaa; Hassan-Zahraee, Mina; Clare, Robert; Gorelick, Kenneth J; Cataldi, Fabio; Watanabe, Mamoru; Hibi, Toshifumi.
Affiliation
  • Saruta M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
  • Park DI; Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim YH; Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Yang SK; Department of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Jang BI; Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea.
  • Cheon JH; Institute of Gastroenterology and Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • Im JP; Division of Gastroenterology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
  • Kanai T; Department of Internal Medicine, Keio University Hospital, Tokyo, Japan.
  • Katsuno T; Department of Gastroenterology, Chiba University Hospital, Chiba, Japan.
  • Ishiguro Y; Department of Gastroenterology and Hematology, National Hospital Organization, Hirosaki National Hospital, Hirosaki, Japan.
  • Nagaoka M; Clinical Research, Pfizer Japan Inc., Tokyo, Japan.
  • Isogawa N; Clinical Statistics, Pfizer Japan Inc., Tokyo, Japan.
  • Li Y; Clinical Pharmacology, Development Japan, Pfizer Japan Inc., Tokyo, Japan.
  • Banerjee A; Clinical Statistics, Pfizer Inc., Cambridge, MA, USA.
  • Ahmad A; Gastroenterology, Pfizer Inc., Cambridge, MA, USA.
  • Hassan-Zahraee M; Early Clinical Research and Development, Pfizer Inc., Cambridge, MA, USA.
  • Clare R; Biotherapeutics Clinical R&D, Pfizer Inc., Collegeville, PA, USA.
  • Gorelick KJ; Biotherapeutics Clinical R&D, Pfizer Inc., Collegeville, PA, USA.
  • Cataldi F; Gastroenterology, Clinical Programs, Pfizer Inc., Cambridge, MA, USA.
  • Watanabe M; Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Hibi T; Center for Advanced IBD Research and Treatment, Kitasato Institute Hospital, Kitasato University, Tokyo, Japan.
Intest Res ; 18(1): 45-55, 2020 Jan.
Article in En | MEDLINE | ID: mdl-32013314
BACKGROUND/AIMS: PF-00547659 is a monoclonal antibody against human mucosal addressin cell adhesion molecule-1 (MAdCAM-1) that prevents the binding of α4ß7+ lymphocytes to MAdCAM-expressing sites in the gastrointestinal tract with high affinity and selectivity, and is being developed for the treatment of Crohn's disease (CD). METHODS: OPERA is a randomized, multicenter, double-blind, placebo-controlled study to investigate the efficacy, safety, and pharmacokinetics of PF-00547659 following subcutaneous administration in subjects with active CD, a history of failure or intolerance to anti-tumor necrosis factor and/or immunosuppressants, high-sensitivity C-reactive protein > 3.0 mg/L, and ulcers on colonoscopy. The primary endpoint was Crohn's Disease Activity Index-70 response at week 8 or 12. Subpopulation analyses for Asian subjects were performed as some differences are observed in genetics and clinical phenotypes in Asian CD patients compared with Western patients. RESULTS: In this study, 265 CD subjects were randomized, with a subpopulation of 21 subjects (8 Japanese and 13 Korean) defined as the Asian population. In the overall and Asian populations; PF-00547659 was pharmacologically active as evidenced by soluble MAdCAM and circulating ß7+ central memory CD4+ T-lymphocytes, although no clear evidence of efficacy was observed in any clinical endpoints; pharmacokinetics of PF-00547659 in the Asian subpopulation was generally comparable to the overall population; and the safety profile of PF-00547659 appeared acceptable up to 12 weeks of treatment. CONCLUSIONS: In the overall and Asian populations, efficacy of PF-00547659 could not be demonstrated using any clinical endpoints compared with placebo. Pharmacokinetics and safety of PF-00547659 were generally comparable. Further studies with larger numbers of patients are required to confirm our results. (Trial Registration Number: NCT01276509).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Intest Res Year: 2020 Document type: Article Affiliation country: Japan Country of publication: Korea (South)

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Intest Res Year: 2020 Document type: Article Affiliation country: Japan Country of publication: Korea (South)