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NCT06269484 · ClinicalTrials.gov registry record · Phase 2

A Phase IIb Study to Evaluate the Safety of Zibotentan/Dapagliflozin in Participants With Cirrhosis-ZEAL-UNLOCK

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
73
Enrollment target

NCT06269484: Completed Phase 2 study, sponsored by AstraZeneca.

NCT06269484 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 73 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06269484, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
73 participants
Enrollment target

Study Summary

This is a Phase IIb multicentre, randomised, double-blind, parallel-group, placebo-controlled study to evaluate the safety of zibotentan/dapagliflozin in combination as compared to zibotentan monotherapy as well as zibotentan/dapagliflozin and zibotentan monotherapy as compared to placebo in patients with cirrhosis.

Primary Outcome

Cumulative number of subjects with event of composite fluid retention endpoint

Interventions

  • DRUG Placebo (placebo matching zibotentan capsule and placebo matching dapagliflozin tablet)
  • DRUG Zibotentan + placebo (placebo matching dapagliflozin tablet)
  • DRUG Zibotentan + dapagliflozin

Trial Details

FieldValue
Enrollment Target 73 participants
Start Date 2024-02-15
Est. Completion 2024-12-11
Phase Phase 2
AstraZeneca

1,285 total trials

What the finished NCT06269484 record still lists

NCT06269484 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 73 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (45% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo (placebo matching zibotentan capsule and placebo matching dapagliflozin tablet) is the first listed.

NCT06269484 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06269484 about?

NCT06269484 is a clinical study titled "A Phase IIb Study to Evaluate the Safety of Zibotentan/Dapagliflozin in Participants With Cirrhosis-ZEAL-UNLOCK". This is a Phase IIb multicentre, randomised, double-blind, parallel-group, placebo-controlled study to evaluate the safety of zibotentan/dapagliflozin in combination as compared to zibotentan monotherapy as well as zibotentan/dapagliflozin and zibotentan monotherapy as compared to placebo in patient...

What is the current status of trial NCT06269484?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 73 participants. The study started on 2024-02-15. Estimated completion is 2024-12-11.

What interventions are being tested in trial NCT06269484?

The interventions under investigation include: Placebo (placebo matching zibotentan capsule and placebo matching dapagliflozin tablet) (DRUG), Zibotentan + placebo (placebo matching dapagliflozin tablet) (DRUG), Zibotentan + dapagliflozin (DRUG).

Who is sponsoring clinical trial NCT06269484?

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 NCT06269484's enrollment target sits among peer trials

73 924th of 2000 higher than 1,076 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT06269484, the US trial registry maintained by the National Library of Medicine. NCT06269484 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.