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ONO-3951 Phase II Study

A multicenter, randomized, double-blind, placebo-controlled, parallel-group study in subjects with irritable bowel syndrome with diarrhea

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080221823
Enrollment
240
Registered
2012-06-13
Start date
2012-06-13
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable bowel syndrome with diarrhea(IBS-D)

Interventions

Sponsors

ONO PHARMACEUTICAL CO.,LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects diagnosed with IBS-D based on the Rome III diagnostic criteria

Exclusion criteria

Exclusion criteria: 1. Presence or history of any of the organic gastrointestinal diseases

Design outcomes

Primary

MeasureTime frame
Percentage of subjects with improvement in abdominal pain

Secondary

MeasureTime frame
Percentage of subjects with improvement in stool frequency, etc.

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026