Study identifier:D9441C00002
ClinicalTrials.gov identifier:NCT06925854
EudraCT identifier:N/A
CTIS identifier:N/A
An open-label, 2-period, 2-sequence cross-over study to assess the effect of AZD4144 on the pharmacokinetics of rosuvastatin in healthy participants
Healthy
Phase 1
Yes
AZD4144, Rosuvastatin
All
12
Interventional
18 Years - 50 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Crossover Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Apr 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Treatment sequence AB Participants will receive single dose of rosuvastatin under fasted condition (Treatment A), followed by a single dose of rosuvastatin with AZD4144 under fasted condition (Treatment B). | Drug: AZD4144 Oral tablet of AZD4144 will be administered. Drug: Rosuvastatin Oral tablet of rosuvastatin will be administered. |
Experimental: Treatment sequence BA Participants will receive a single dose of rosuvastatin with AZD4144 under fasted condition (Treatment B), followed by a single dose of rosuvastatin under fasted condition (Treatment A). | Drug: AZD4144 Oral tablet of AZD4144 will be administered. Drug: Rosuvastatin Oral tablet of rosuvastatin will be administered. |