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NCT06502379 · ClinicalTrials.gov registry record · Phase 1

A Single and Multiple Ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of AZD8965 in Healthy Participants (Including Japanese and Chinese Participants) and an Open-label Cohort to Assess the Effect of Food on the Pharmacokinetics of AZD8965 in Healthy Participants

A Phase 1 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 1
Development phase
147
Enrollment target

NCT06502379: Completed Phase 1 study, sponsored by AstraZeneca.

NCT06502379 is a Phase 1 study that has completed, run by AstraZeneca. The registered enrollment target is 147 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (145% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06502379, a Phase 1 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 1
Development phase
147 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics (PK) of AZD8965 via single and multiple ascending doses in healthy participants (including Japanese and Chinese participants), and to assess the effect of food on the safety, tolerability, and PK of orally administered AZD8965.

Primary Outcome

To assess the safety and tolerability of AZD8965 following oral administration of single ascending doses to healthy participants.

Interventions

  • OTHER Placebo
  • DRUG AZD8965

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2024-08-02
Est. Completion 2025-11-15
Phase Phase 1
AstraZeneca

1,285 total trials

What the finished NCT06502379 record still lists

NCT06502379 is an interventional study that assigns participants to a tested intervention. The registered 147 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (145% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT06502379 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06502379 about?

NCT06502379 is a clinical study titled "A Single and Multiple Ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of AZD8965 in Healthy Participants (Including Japanese and Chinese Participants) and an Open-label Cohort to Assess the Effect of Food on the Pharmacokinetics of AZD8965 in Healthy Participants". The purpose of this study is to assess the safety, tolerability, and pharmacokinetics (PK) of AZD8965 via single and multiple ascending doses in healthy participants (including Japanese and Chinese participants), and to assess the effect of food on the safety, tolerability, and PK of orally administ...

What is the current status of trial NCT06502379?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 147 participants. The study started on 2024-08-02. Estimated completion is 2025-11-15.

What interventions are being tested in trial NCT06502379?

The interventions under investigation include: Placebo (OTHER), AZD8965 (DRUG).

Who is sponsoring clinical trial NCT06502379?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06502379's enrollment target sits among peer trials

147 387th of 2000 higher than 1,610 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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Source: ClinicalTrials.gov NCT06502379, the US trial registry maintained by the National Library of Medicine. NCT06502379 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.