Overview

A Study to Investigate Multiple Ascending Doses and Relative Bioavailability of AZD5004 in Healthy Participants

Status:
COMPLETED
Trial end date:
2025-03-06
Target enrollment:
Participant gender:
Summary
The main purpose of this study is to assess the safety, tolerability, and pharmacokinetic (PK) of AZD5004 administered as multiple oral doses in healthy participants and to compare the relative bioavailability of two oral tablet strengths of AZD5004.
Phase:
PHASE1
Details
Lead Sponsor:
AstraZeneca