drugset / Trial / NCT05702463

Assessing Pharmacokinetics and Pharmacodynamics of Daily Enteric-coated Aspirin in Patients With StablE Diabetes II

NCT05702463

RandomizedCrossoverOpen-labelPrevention

Summary

This phase 2 study will include patients suffering from type 2 diabetes mellitus and will first study their response to enteric coated aspirin at a dose of 80 mg per day for a 7-day period. Participants with an incomplete platelet inhibition after exposure to EC aspirin at doses of 80 mg once daily will be randomized to a random order of 3 different ASA regimens: EC ASA 162 mg once daily, EC ASA 81 mg twice daily and chewable ASA 40 mg twice daily. The aims are to determine the feasibility of a larger scale trial, and to determine the regimen associated with the lowest proportion of non-responders after randomization. Platelet function will be assessed at baseline and at day 7 of each arms of the study.

Timeline

Start
2023-06-13
Primary completion
2027-06-01
Completion
2027-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Aspirin Small molecule 40 mg
Subject Aspirin Small molecule 81 mg
Subject Aspirin Small molecule 162 mg