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NCT06948747 · ClinicalTrials.gov registry record · Phase 1

A Study to Investigate the Effect of AZD5004 on Rosuvastatin, Atorvastatin, Simvastatin, Repaglinide and the Effect of Erythromycin on AZD5004 in Healthy Participants

A Phase 1 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 1
Development phase
49
Enrollment target

NCT06948747: Completed Phase 1 study, sponsored by AstraZeneca.

NCT06948747 is a Phase 1 study that has completed, run by AstraZeneca. The registered enrollment target is 49 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06948747, a Phase 1 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

This study will assess the effect of AZD5004 on Rosuvastatin, Atorvastatin, Simvastatin, Repaglinide and the effect of Erythromycin on AZD5004 in healthy adult male and female participants.

Primary Outcome

Part A: To assess the effect of single dose of AZD5004 on the PK of a single dose of rosuvastatin and multiple doses of erythromycin on the PK of a single dose of AZD5004 in healthy participants. Part B: To assess the effect of multiple doses of AZD5004 on the PK of a single dose of atorvastatin and atorvastatin metabolites (o-hydroxy atorvastatin and p-hydroxy atorvastatin) and simvastatin and simvastatin metabolites (simvastatin acid) in healthy participants. Part C: To assess the effect of

Interventions

  • DRUG Rosuvastatin
  • DRUG Erythromycin
  • DRUG Simvastatin
  • DRUG AZD5004
  • DRUG Atorvastatin

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2025-05-06
Est. Completion 2025-10-03
Phase Phase 1
AstraZeneca

1,285 total trials

What the finished NCT06948747 record still lists

NCT06948747 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower).

The record links to 0 conditions, and to 5 interventions - of which Rosuvastatin is the first listed.

NCT06948747 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06948747 about?

NCT06948747 is a clinical study titled "A Study to Investigate the Effect of AZD5004 on Rosuvastatin, Atorvastatin, Simvastatin, Repaglinide and the Effect of Erythromycin on AZD5004 in Healthy Participants". This study will assess the effect of AZD5004 on Rosuvastatin, Atorvastatin, Simvastatin, Repaglinide and the effect of Erythromycin on AZD5004 in healthy adult male and female participants.

What is the current status of trial NCT06948747?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2025-05-06. Estimated completion is 2025-10-03.

What interventions are being tested in trial NCT06948747?

The interventions under investigation include: Rosuvastatin (DRUG), Erythromycin (DRUG), Simvastatin (DRUG), AZD5004 (DRUG), Atorvastatin (DRUG).

Who is sponsoring clinical trial NCT06948747?

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 NCT06948747's enrollment target sits among peer trials

49 1017th of 2000 higher than 976 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 NCT06948747, the US trial registry maintained by the National Library of Medicine. NCT06948747 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.