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NCT05186129

Bioequivalence Study of Clopid® (Clopidogrel) 75 mg Tablet and Plavix® 75 mg Tablet After Oral Administration to Healthy Adult Subjects Under Fasting Condition

Completed Phase 1 Last updated 2 March 2022
What this trial tests

Phase 1 trial testing Clopid® 75 mg Tablet in Bioequivalence in 36 participants. Completed in 20 April 2018.

Timeline
6 April 2018
Primary endpoint
15 April 2018
20 April 2018

Quick facts

Lead sponsorCenter for Bioequivalence Studies and Clinical Research
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposeother
Enrollment36
Start date6 April 2018
Primary completion15 April 2018
Estimated completion20 April 2018
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Center for Bioequivalence Studies and Clinical Research

Who can join

Adults 18 to 55, male only, with Bioequivalence. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To compare the rate and extent of absorption of Clopid® (Clopidogrel) 75 mg Tablet and Plavix® (clopidogrel) 75 mg tablet under fasting condition.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Bioequivalence

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05186129.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing