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Adrenomedullin for biologic-resistant Crohn's disease: A randomized, double-blind, placebo-controlled phase 2a clinical trial.
Kita, Toshihiro; Ashizuka, Shinya; Takeda, Teruyuki; Matsumoto, Takayuki; Ohmiya, Naoki; Nakase, Hiroshi; Motoya, Satoshi; Ohi, Hidehisa; Mitsuyama, Keiichi; Hisamatsu, Tadakazu; Kanmura, Shuji; Kato, Naoya; Ishihara, Shunji; Nakamura, Masanao; Moriyama, Tomohiko; Saruta, Masayuki; Nozaki, Ryoichi; Yamamoto, Shojiro; Inatsu, Haruhiko; Watanabe, Koji; Kitamura, Kazuo.
Affiliation
  • Kita T; Department of Projects Research, Frontier Science Research Center, University of Miyazaki, Miyazaki, Japan.
  • Ashizuka S; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Takeda T; Department of Gastroenterology, Fukuoka University Chikushi Hospital, Fukuoka, Japan.
  • Matsumoto T; Division of Gastroenterology, Department of Internal Medicine, School of Medicine, Iwate Medical University, Morioka, Japan.
  • Ohmiya N; Department of Gastroenterology, Fujita Health University School of Medicine, Toyoake, Japan.
  • Nakase H; Department of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Motoya S; IBD Center, Sapporo Kosei General Hospital, Hokkaido, Japan.
  • Ohi H; Department of Gastroenterology, Idzuro Imamura Hospital, Kagoshima, Japan.
  • Mitsuyama K; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
  • Hisamatsu T; Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Mitaka, Japan.
  • Kanmura S; Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Kato N; Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Ishihara S; Department of Gastroenterology, Shimane University Hospital, Izumo, Japan.
  • Nakamura M; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Moriyama T; Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Saruta M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
  • Nozaki R; Coloproctology Center Takano Hospital, Kumamoto, Japan.
  • Yamamoto S; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Inatsu H; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Watanabe K; Department of Projects Research, Frontier Science Research Center, University of Miyazaki, Miyazaki, Japan.
  • Kitamura K; Department of Projects Research, Frontier Science Research Center, University of Miyazaki, Miyazaki, Japan.
J Gastroenterol Hepatol ; 37(11): 2051-2059, 2022 Nov.
Article in En | MEDLINE | ID: mdl-35840351
BACKGROUND AND AIM: Adrenomedullin is a bioactive peptide with many pleiotropic effects, including mucosal healing and immunomodulation. Adrenomedullin has shown beneficial effects in rodent models of inflammatory bowel disease and, more importantly, in clinical trials including patients with ulcerative colitis. We performed a successive clinical trial to investigate the efficacy and safety of adrenomedullin in patients with Crohn's disease (CD). METHODS: This was a multicenter, double-blind, placebo-controlled phase 2a trial that evaluated 24 patients with biologic-resistant CD in Japan. Patients were randomly assigned to three groups and were given an infusion of 10 or 15 ng/kg/min of adrenomedullin or placebo for 8 h per day for 7 days. The primary endpoint was the change in the CD activity index (CDAI) at 8 weeks. The main secondary endpoints included changes in CDAI from week 4 to week 24. RESULTS: No differences in the primary or secondary endpoints were observed between the three groups by the 8th week. Changes in CDAI in the placebo group gradually decreased and disappeared at 24 weeks, but those in the adrenomedullin-treated groups (10 or 15 ng/kg/min group) remained at steady levels for 24 weeks. Therefore, a significant difference was observed between the placebo and adrenomedullin-treated groups at 24 weeks (P = 0.043) in the mixed-effects model. We noted mild adverse events caused by the vasodilatory effect of adrenomedullin. CONCLUSION: In this trial, we observed a long-lasting (24 weeks) decrease in CDAI in the adrenomedullin-treated groups. Adrenomedullin might be beneficial for biologic-resistant CD, but further research is needed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / Crohn Disease Type of study: Clinical_trials Limits: Humans Country/Region as subject: Asia Language: En Journal: J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2022 Document type: Article Affiliation country: Japan Country of publication: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / Crohn Disease Type of study: Clinical_trials Limits: Humans Country/Region as subject: Asia Language: En Journal: J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2022 Document type: Article Affiliation country: Japan Country of publication: Australia