Literature DB >> 23881665

Acotiamide: first global approval.

Mary L Nowlan, Mary L Nolan1, Lesley J Scott.   

Abstract

Acotiamide (Acofide(®)), an oral first-in-class prokinetic drug, is under global development by Zeria Pharmaceutical Co. Ltd and Astellas Pharma Inc. for the treatment of patients with functional dyspepsia. The drug modulates upper gastrointestinal motility to alleviate abdominal symptoms resulting from hypomotility and delayed gastric emptying. It exerts its activity in the stomach via muscarinic receptor inhibition, resulting in enhanced acetylcholine release and inhibition of acetylcholinesterase activity. Unlike other prokinetic drugs that are utilized in the management of functional dyspepsia, acotiamide shows little/no affinity for serotonin or dopamine D2 receptors. Acotiamide is the world's first approved treatment for functional dyspepsia diagnosed by Rome III criteria, with its first approval occurring in Japan. Phase III trials in this patient population are in preparation in Europe, with phase II trials completed in the USA and Europe. This article summarizes the milestones in the development of acotiamide, leading to its first approval for use in patients with functional dyspepsia.

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Year:  2013        PMID: 23881665     DOI: 10.1007/s40265-013-0100-9

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  22 in total

1.  Z-338, a newly synthetized carboxyamide derivative, stimulates gastric motility through enhancing the excitatory neurotransmission.

Authors:  T Nakajima; H Nawata; Y Ito
Journal:  J Smooth Muscle Res       Date:  2000-04

2.  A long-term study of acotiamide in patients with functional dyspepsia: results from an open-label phase III trial in Japan on efficacy, safety and pattern of administration.

Authors:  K Matsueda; M Hongo; S Ushijima; H Akiho
Journal:  Digestion       Date:  2011-09-21       Impact factor: 3.216

Review 3.  Review article: current treatment options and management of functional dyspepsia.

Authors:  B E Lacy; N J Talley; G R Locke; E P Bouras; J K DiBaise; H B El-Serag; B P Abraham; C W Howden; P Moayyedi; C Prather
Journal:  Aliment Pharmacol Ther       Date:  2012-05-16       Impact factor: 8.171

4.  Acotiamide hydrochloride (Z-338) enhances gastric motility and emptying by inhibiting acetylcholinesterase activity in rats.

Authors:  Masanao Kawachi; Yugo Matsunaga; Takao Tanaka; Yuko Hori; Katsunori Ito; Kenji Nagahama; Tomoko Ozaki; Naonori Inoue; Ryoko Toda; Kazuyoshi Yoshii; Masamichi Hirayama; Yoshihiro Kawabata; Mineo Takei
Journal:  Eur J Pharmacol       Date:  2011-06-01       Impact factor: 4.432

Review 5.  Acotiamide (Z-338) as a possible candidate for the treatment of functional dyspepsia.

Authors:  H Suzuki; T Hibi
Journal:  Neurogastroenterol Motil       Date:  2010-06       Impact factor: 3.598

6.  Characterization of functional effects of Z-338, a novel gastroprokinetic agent, on the muscarinic M1, M2, and M3 receptors expressed in Xenopus oocytes.

Authors:  Y Doi; O Murasaki; M Kaibara; Y Uezono; H Hayashi; K Yano; K Taniyama
Journal:  Eur J Pharmacol       Date:  2004-11-28       Impact factor: 4.432

Review 7.  Current management strategies and emerging treatments for functional dyspepsia.

Authors:  Michael Camilleri; Vincenzo Stanghellini
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2013-02-05       Impact factor: 46.802

8.  Acotiamide hydrochloride (Z-338), a novel prokinetic agent, restores delayed gastric emptying and feeding inhibition induced by restraint stress in rats.

Authors:  K Seto; T Sasaki; K Katsunuma; N Kobayashi; K Tanaka; J Tack
Journal:  Neurogastroenterol Motil       Date:  2008-05-09       Impact factor: 3.598

9.  A dose-ranging, placebo-controlled, pilot trial of Acotiamide in patients with functional dyspepsia.

Authors:  J Tack; A Masclee; R Heading; A Berstad; H Piessevaux; T Popiela; A Vandenberghe; H Kato
Journal:  Neurogastroenterol Motil       Date:  2009-03       Impact factor: 3.598

Review 10.  Current management of functional dyspepsia: impact of Rome III subdivision.

Authors:  Georgios P Karamanolis; Jan Tack
Journal:  Ann Gastroenterol       Date:  2012
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  5 in total

1.  Physiologically-Based Pharmacokinetic and Pharmacodynamic Modeling for the Inhibition of Acetylcholinesterase by Acotiamide, A Novel Gastroprokinetic Agent for the Treatment of Functional Dyspepsia, in Rat Stomach.

Authors:  Kazuyoshi Yoshii; Minami Iikura; Masamichi Hirayama; Ryoko Toda; Yoshihiro Kawabata
Journal:  Pharm Res       Date:  2015-09-09       Impact factor: 4.200

2.  MOST: most-similar ligand based approach to target prediction.

Authors:  Tao Huang; Hong Mi; Cheng-Yuan Lin; Ling Zhao; Linda L D Zhong; Feng-Bin Liu; Ge Zhang; Ai-Ping Lu; Zhao-Xiang Bian
Journal:  BMC Bioinformatics       Date:  2017-03-11       Impact factor: 3.169

3.  Sulfur-containing therapeutics in the treatment of Alzheimer's disease.

Authors:  Haizhou Zhu; Venkateshwara Dronamraju; Wei Xie; Swati S More
Journal:  Med Chem Res       Date:  2021-01-15       Impact factor: 1.965

4.  Effects of acotiamide on esophageal motor function and gastroesophageal reflux in healthy volunteers.

Authors:  Norihisa Ishimura; Mami Mori; Hironobu Mikami; Shino Shimura; Goichi Uno; Masahito Aimi; Naoki Oshima; Shunji Ishihara; Yoshikazu Kinoshita
Journal:  BMC Gastroenterol       Date:  2015-09-11       Impact factor: 3.067

5.  Uncovering the Mechanisms of Chinese Herbal Medicine (MaZiRenWan) for Functional Constipation by Focused Network Pharmacology Approach.

Authors:  Tao Huang; Ziwan Ning; Dongdong Hu; Man Zhang; Ling Zhao; Chengyuan Lin; Linda L D Zhong; Zhijun Yang; Hongxi Xu; Zhaoxiang Bian
Journal:  Front Pharmacol       Date:  2018-03-26       Impact factor: 5.810

  5 in total

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