Study identifier:D9441C00004
ClinicalTrials.gov identifier:NCT06942923
EudraCT identifier:N/A
CTIS identifier:2024-519414-31-00
A Phase I, Randomised, Investigator- and Participant-blinded, Placebo-Controlled, Study to Assess the Safety, Tolerability, and Pharmacodynamics of AZD4144 in Participants with Obesity
Healthy Participants
Phase 1
Yes
AZD4144, Placebo
All
28
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Apr 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZD4144 Participants will receive a single oral dose of AZD4144 under fasted conditions once daily for 28 days. | Drug: AZD4144 AZD4144 will be administered orally as per arms they have been assigned. |
Placebo Comparator: Placebo Participants will receive a single oral dose of matching placebo to AZD4144 under fasted conditions once daily for 28 days. | Drug: Placebo Placebo will be administered orally as per arms they have been assigned. |