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NCT05864391 · ClinicalTrials.gov registry record · Phase 1
A Study to Investigate Safety, Tolerability, and Pharmacokinetics of AZD7503 in Participants With Suspected NASH.
A Phase 1 study, sponsored by AstraZeneca.
- Terminated
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT05864391: Clinical Trial Phase 1 study, sponsored by AstraZeneca.
NCT05864391 is a Phase 1 study that was terminated before completion, run by AstraZeneca. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05864391, a Phase 1 study, was terminated before completion, sponsored by AstraZeneca.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to measure the safety, tolerability, and PK (measurement of drug activity in the body over time) of AZD7503 injected subcutaneously, and compared to placebo, in participants with suspected NASH, a type of liver disease.
Primary Outcome
AEs will be collected at all sites visits per SOA.
Interventions
- DRUG AZD7503
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2023-03-31 |
| Est. Completion | 2024-03-20 |
| Phase | Phase 1 |
Why NCT05864391 stopped before completion
NCT05864391 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).
The record links to 0 conditions, and to 1 intervention - of which AZD7503 is the first listed.
NCT05864391 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05864391 about?
NCT05864391 is a clinical study titled "A Study to Investigate Safety, Tolerability, and Pharmacokinetics of AZD7503 in Participants With Suspected NASH.". The purpose of this study is to measure the safety, tolerability, and PK (measurement of drug activity in the body over time) of AZD7503 injected subcutaneously, and compared to placebo, in participants with suspected NASH, a type of liver disease.
What is the current status of trial NCT05864391?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2023-03-31. Estimated completion is 2024-03-20.
What interventions are being tested in trial NCT05864391?
The interventions under investigation include: AZD7503 (DRUG).
Who is sponsoring clinical trial NCT05864391?
This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05864391's enrollment target sits among peer trials
40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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