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YM060 (Tablets) Phase III Clinical Trial - Multicenter, Double-Blind, Parallel Group-Comparative Study in Patients with Diarrhea-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.
NCT00189696

Astellas Study ID

The unique identification code given by the study sponsor.

060-CL-202

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

Irritable Bowel Syndrome (IBS)

Phase

These clinical trials are done to confirm that an experimental treatment helps participants who have a specific condition. These clinical trials often compare the experimental treatment to another treatment or, if appropriate, a placebo.

Phase 3

Age

N/A

Sex

N/A

Product

ramosetron hydrochloride

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 2004 - Jul 2005

Masking

Not Available

YM060 (Tablets) Phase III Clinical Trial - Multicenter, Double-Blind, Parallel Group-Comparative Study in Patients with Diarrhea-Predominant Irritable Bowel Syndrome

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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