Trial Profile

A Phase I, Two-Part Study in Healthy Volunteers Consisting of a Randomized, Single-blind, Placebo-controlled Multiple Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of AZD5004 and a Randomized, Open-Label, Two-way Cross-over Study to Compare the Relative Bioavailability of Two Oral Tablet Strengths of AZD5004

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 20 Mar 2025

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At a glance

Drugs AZD 5004 (Primary)
Indications Non-alcoholic steatohepatitis; Obesity; Type 2 diabetes mellitus
Focus Adverse reactions; Pharmacokinetics
Sponsors AstraZeneca

17 Mar 2025 Status changed from active, no longer recruiting to completed.
17 Dec 2024 Planned End Date changed from 3 Mar 2025 to 27 Feb 2025.
17 Dec 2024 Planned primary completion date changed from 3 Mar 2025 to 27 Feb 2025.

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