A Study of Oral Dosing of ASP0456 in Patients With Chronic Constipation

Status Completed

Clinical Trial Summary

The objective of this study is to verify the efficacy and investigate the safety of the study drug when ASP0456 is administered orally for 4 weeks and 52 weeks.

Clinical Trial Description

This study consists of two parts. In Part I, ASP0456 or placebo will be administered orally in a blind manner. In Part II, the long-term safety and efficacy of ASP0456 will be evaluated in patients who have participated in the study and completed the Part I. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02809105
Study type	Interventional
Source	Astellas Pharma Inc
Contact
Status	Completed
Phase	Phase 3
Start date	June 24, 2016
Completion date	November 10, 2017

View Details

See also
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