drugset / Trial / NCT06491550

A Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD4144 as Well as the Impact of AZD4144 on the Pharmacokinetics of Rosuvastatin and Furosemide in Healthy Participants

NCT06491550

Phase 1 Completed 91 enrolled AstraZeneca
RandomizedSequentialTriple-blindTreatment

Summary

This study consists of 3 parts: Part A, Part B and Part C. This study will compare the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of AZD4144 with placebo in healthy participants, in Part A and Part B. Part C of this study will investigate the possibility of drug-drug interaction (DDI) between IV AZD4144 and oral rosuvastatin and furosemide by evaluating the PK of rosuvastatin and furosemide when administered alone and in combination with single IV dose of AZD4144

Timeline

Start
2024-07-15
Primary completion
2025-06-11
Completion
2025-06-11

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD4144 Unknown Intravenous
Subject Furosemide Other / unclassified 1 mg Oral
Subject Rosuvastatin Small molecule 10 mg Oral

Indications

No indication recorded.