Terminated PHASE3 INTERVENTIONAL 2-arm NCT00557921

Clopidogrel and the Optimization of Gastrointestinal Events (COGENT-1) (COGENT-1)

A Randomized, Double-Blind, Double-Dummy, Parallel Group, Phase 3 Efficacy and Safety Study of CGT-2168 Compared With Clopidogrel to Reduce Upper Gastrointestinal Events Including Bleeding and Symptomatic Ulcer Disease

Sponsor: Cogentus Pharmaceuticals

Conditions Acute Coronary Syndrome Coronary Artery Disease Myocardial Infarction Percutaneous Coronary Intervention

Interventions CGT-2168 (clopidogrel 75 mg/omeprazole 20 mg) and aspirin Plavix (clopidogrel 75 mg) and aspirin

Updated 2 times since 2024 Last updated: Jan 27, 2009 Started: Dec 31, 2007 Primary completion: Nov 30, 2009 Completion: Nov 30, 2009

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Terminated by Sponsor

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Listed as NCT00557921, this PHASE3 trial focuses on Acute Coronary Syndrome and Coronary Artery Disease and remains terminated or withdrawn. Sponsored by Cogentus Pharmaceuticals, it has been updated 2 times since 2007, reflecting limited change activity. This study contributes longitudinal data to the cardiovascular research landscape.

Status Flow

Change History

2 versions recorded

Sep 2025 — Present [monthly]

Terminated PHASE3
Sep 2024 — Sep 2025 [monthly]

Terminated PHASE3

First recorded

Dec 2007

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Cogentus Pharmaceuticals

Data source: Cogentus Pharmaceuticals

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

Abington, United States , Aguascalientes, Mexico , Albany, United States , Albi, France , Alexander City, United States , Anaheim, United States , Anderson, United States , Antofagasta, Chile , Arlington, United States , Asheville, United States and 387 more locations