Clinical Trial

Comparative Bioavailability Study Between Ticagrelor and ASA Administered Individually or in Combination.

Completed Phase 1
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Summary
Study conducted to determine and compare the relative bioavailability of two solid oral formulations (reference versus test) of the non-fixed combination of Ticagrelor 90 mg (Brilinta by AstraZeneca S.A. de C.V.) + Acetylsalicylic Acid 100 mg (ASPIRINA JUNIOR by Bayer de México S.A. de C.V.) administered concomitantly versus the fixed-dose combination of Ticagrelor 90 mg / Acetylsalicylic Acid 100 mg manufactured by Laboratorios Silanes S.A. de C.V.
Trial Details
NCT Number NCT07444164
Lead Sponsor Laboratorios Silanes S.A. de C.V.
Conditions Healthy
Enrollment 24 participants
Start Date 2025-01-13
Primary Completion 2025-01-23 (estimated)
Study Completion 2025-02-05 (estimated)
Updated on ClinicalTrials.gov 2026-03-02