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

PHASE1CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

August 15, 2024

Primary Completion Date

March 6, 2025

Study Completion Date

March 6, 2025

Conditions
Healthy Participants
Interventions
DRUG

AZD5004

Participants will receive oral tablets of AZD5004 in Part A and Part B of the study as per arms they are assigned.

DRUG

Placebo

Placebo will be administered as an oral tablet once daily.

Trial Locations (1)

21225

Research Site, Brooklyn

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY