Dose finding study of mosapride in functional dyspepsia: a placebo-controlled, randomized study
Version of Record online: 27 APR 2002
Alimentary Pharmacology & Therapeutics
Volume 16, Issue 5, pages 959–967, May 2002
How to Cite
Hallerbäck, B. I. , Bommelaer, G. , Bredberg, E. , Campbell, M. , Hellblom, M. , Lauritsen, K. , Wienbeck, M. and Holmgren, L. .-L. (2002), Dose finding study of mosapride in functional dyspepsia: a placebo-controlled, randomized study. Alimentary Pharmacology & Therapeutics, 16: 959–967. doi: 10.1046/j.1365-2036.2002.01236.x
- Issue online: 27 APR 2002
- Version of Record online: 27 APR 2002
Prokinetic agents have shown variable efficacy in the treatment of functional dyspepsia. Mosapride is a new prokinetic 5-hydroxytryptamine-4 agonistic agent.
To evaluate the efficacy of three dosage regimens of mosapride compared with placebo in the treatment of functional dyspepsia.
Patients were randomly allocated to treatment with placebo or mosapride (5 mg b.d., 10 mg b.d. or 7.5 mg t.d.s.) in a double-blind, prospective, multicentre, multinational study. The change in symptom severity score from an untreated baseline week to the sixth week of treatment was used to compare treatment efficacy.
There were 141, 140, 143 and 142 patients valid for evaluation in the intention-to-treat population in the placebo, mosapride 5 mg b.d., mosapride 10 mg b.d. and mosapride 7.5 mg t.d.s. groups, respectively. The mean changes in the overall dyspeptic symptom score were – 0.90, – 0.94, – 0.88 and – 0.89, respectively, and the proportions of patients feeling better at the end of the treatment period were 60%, 59%, 59% and 61%, respectively. No statistically significant difference was seen.
Treatment of functional dyspepsia with mosapride was not superior to placebo. The result raises the question of whether treatment with prokinetic agents is appropriate for functional dyspepsia.