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A study to evaluate the effect of ASP0456 in patients with constipation predominant irritable bowel syndrome

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT01714843

Astellas Study ID

The unique identification code given by the study sponsor.

0456-CL-0021

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Follow Trial

Condition

Constipation

Phase

These clinical trials are done to learn if an experimental treatment helps participants who have a specific condition or disease. Phase 2 trials usually include a larger group of participants than Phase 1 trials.

Phase 2

Age

20 years - 64 years

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Aug 2012 - Dec 2013

Masking

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Enrollment number

559

Phase II study of ASP0456 - A Double-blind, Placebo-controlled, Parallel-group, Comparative Study in Patients with Constipation-predominant Irritable Bowel Syndrome

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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