TY - JOUR
T1 - Adrenomedullin for steroid-resistant ulcerative colitis
T2 - a randomized, double-blind, placebo-controlled phase-2a clinical trial
AU - Kita, Toshihiro
AU - Ashizuka, Sinya
AU - Ohmiya, Naoki
AU - Yamamoto, Takayuki
AU - Kanai, Takanori
AU - Motoya, Satoshi
AU - Hirai, Fumihito
AU - Nakase, Hiroshi
AU - Moriyama, Tomohiko
AU - Nakamura, Masanao
AU - Suzuki, Yasuo
AU - Kanmura, Shuji
AU - Kobayashi, Taku
AU - Ohi, Hidehisa
AU - Nozaki, Ryoichi
AU - Mitsuyama, Keiichi
AU - Yamamoto, Shojiro
AU - Inatsu, Haruhiko
AU - Watanabe, Koji
AU - Hibi, Toshifumi
AU - Kitamura, Kazuo
N1 - Funding Information:
The authors would like to thank all the attending physicians in this trial. Tomomi Yamashima, Sae Miyaushiro, Remi Yonezawa, Ichiro Sannomiya, Koji Nakashima: Division of Circulatory and Body Fluid Regulation, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Japan; Emi Yonezawa: Department of Gastroenterology and Hematology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan; Takeshi Yamamura: Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Keiko Maeda, Tsunaki Sawada: Department of Endoscopy, Nagoya University Hospital, Nagoya, Japan; Takahiro Shimoyama: IBD Center, Yokkaichi Hazu Medical Center, Yokkaichi, Japan; Tomoe Kazama: Department of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine, Sapporo, Japan
Funding Information:
This study was funded by the Japanese Agency for Medical Research and Development (AMED), Practical Research Project for Rare/Intractable Diseases, JP17ek0109089. Acknowledgements
Publisher Copyright:
© 2020, The Author(s).
PY - 2021/2
Y1 - 2021/2
N2 - Background: Adrenomedullin (AM) is a bioactive peptide having many pleiotropic effects, including mucosal healing and immunomodulation. AM has shown beneficial effects in rodent models and in preliminary study for patients with ulcerative colitis (UC). We performed a clinical trial to investigate the efficacy and safety of AM in patients with UC. Methods: This was a multi-center, double-blind, placebo-controlled phase-2a trial evaluating 28 patients in Japan with steroid-resistant UC. Patients were randomly assigned to four groups and given an infusion of 5, 10, 15 ng/kg/min of AM or placebo for 8 h per day for 14 days. The primary endpoint was the change in Mayo scores at 2 weeks. Main secondary endpoints included the change in Mayo scores and the rate of clinical remission at 8 weeks, defined as a Mayo score 0. Results: No differences in the primary or secondary endpoints were observed among the four groups at 2 weeks. Despite the insufficient tracking rate, the Mayo score at 8 weeks was only significantly decreased in the high-dose AM group (15 ng/kg/min) compared with the placebo group (− 9.3 ± 1.2 vs. − 3.0 ± 2.8, P = 0.035), with its rate of clinical remission at 8 weeks being significantly higher (3/3, 100% vs. 0/2, 0%, P = 0.025). We noted mild but no serious adverse events caused by the vasodilatory effect of AM. Conclusions: In this double-blind randomized trial, we observed the complete remission at 8 weeks in patients with steroid-resistant UC receiving a high dose of AM. Clinical trial registry: JAPIC clinical trials information; Japic CTI-205255 (200410115290). https://www.clinicaltrials.jp/cti-user/trial/Search.jsp.
AB - Background: Adrenomedullin (AM) is a bioactive peptide having many pleiotropic effects, including mucosal healing and immunomodulation. AM has shown beneficial effects in rodent models and in preliminary study for patients with ulcerative colitis (UC). We performed a clinical trial to investigate the efficacy and safety of AM in patients with UC. Methods: This was a multi-center, double-blind, placebo-controlled phase-2a trial evaluating 28 patients in Japan with steroid-resistant UC. Patients were randomly assigned to four groups and given an infusion of 5, 10, 15 ng/kg/min of AM or placebo for 8 h per day for 14 days. The primary endpoint was the change in Mayo scores at 2 weeks. Main secondary endpoints included the change in Mayo scores and the rate of clinical remission at 8 weeks, defined as a Mayo score 0. Results: No differences in the primary or secondary endpoints were observed among the four groups at 2 weeks. Despite the insufficient tracking rate, the Mayo score at 8 weeks was only significantly decreased in the high-dose AM group (15 ng/kg/min) compared with the placebo group (− 9.3 ± 1.2 vs. − 3.0 ± 2.8, P = 0.035), with its rate of clinical remission at 8 weeks being significantly higher (3/3, 100% vs. 0/2, 0%, P = 0.025). We noted mild but no serious adverse events caused by the vasodilatory effect of AM. Conclusions: In this double-blind randomized trial, we observed the complete remission at 8 weeks in patients with steroid-resistant UC receiving a high dose of AM. Clinical trial registry: JAPIC clinical trials information; Japic CTI-205255 (200410115290). https://www.clinicaltrials.jp/cti-user/trial/Search.jsp.
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U2 - 10.1007/s00535-020-01741-4
DO - 10.1007/s00535-020-01741-4
M3 - Article
C2 - 33140199
AN - SCOPUS:85094952274
SN - 0944-1174
VL - 56
SP - 147
EP - 157
JO - Journal of Gastroenterology
JF - Journal of Gastroenterology
IS - 2
ER -