drugset / Trial / NCT06381466

A Study to Investigate Safety, Tolerability, and Pharmacokinetics of Oral AZD0233 Compared With Placebo in Healthy Adult Participants.

NCT06381466 ↗

Phase 1 Terminated 84 enrolled AstraZeneca Parexel · collab
RandomizedSequentialTriple-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of AZD0233 following single and multiple ascending dose (SAD and MAD) administration in healthy participants.

Timeline

Start
2024-04-01
Primary completion
2025-12-30
Completion
2025-12-30

Outcome

Outcome not reported

Stopped: “The study has been terminated due to adverse finding in a non-clinical, chronic toxicology study.”

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD0233 Unknown — Oral