CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 63 enrolled
Drug / intervention
SYN-010 21 mg +2 moredrug
Likely dose
SYN-010 21 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02495623
NCT02495623Phase 2Completed

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multi-Dose Study of the Effect of Two Dosage Strengths of SYN-010 Compared With Placebo on Breath Methane Production in Breath Methane-Positive Subjects With IBS-C

Theriva Biologics, Inc.·interventional·Posted Jul 13, 2015·Updated Nov 27, 2018

In Brief

A Phase 2 clinical trial evaluating SYN-010 21 mg, SYN-010 42 mg, and 1 other intervention for Irritable Bowel Syndrome With Constipation (IBS-C). Completed, enrolled 63 participants across 1 site.

Detailed Summary

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multi-Dose Study of the Effect of Two Dosage Strengths of SYN-010 Compared with Placebo on Breath Methane Production in Breath Methane-Positive Subjects with Irritable Bowel Syndrome with Constipation (IBS-C)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedJul 13, 2015
Enrollment StartJun 1, 2015
Primary CompletionOct 1, 2015
Study CompletionNov 1, 2015
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 11.0 years ago

Interventions

SYN-010 21 mgdrug

SYN-010 42 mgdrug

Placebodrug