A Study to Investigate the Effect of Oral Ticagrelor on the Pharmacokinetics of Oral Rosuvastatin When Given in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

August 5, 2024

Primary Completion Date

October 8, 2024

Study Completion Date

October 8, 2024

Conditions
Healthy Participants
Interventions
DRUG

Rosuvastatin

Participants will receive rosuvastatin (dose 1 or dose 2) orally as a single dose on Day 1 in Period 1 and Day 6 in Period 2.

DRUG

Ticagrelor

Participants in each arm will receive ticagrelor 90 mg orally BID from Day 6 to Day 10.

Trial Locations (1)

14050

Research Site, Berlin

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY