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NCT07343960 · ClinicalTrials.gov registry record · Phase 1

A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment

A Phase 1 study of Moderate Hepatic Impairment, sponsored by AstraZeneca.

Recruiting
Registry status
Phase 1
Development phase
20
Enrollment target
2
Study locations

NCT07343960: Recruiting Phase 1 study of Moderate Hepatic Impairment, sponsored by AstraZeneca.

NCT07343960 is a Phase 1 study of Moderate Hepatic Impairment that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 20 participants, roughly in line with the 21-participant average among 4 other Moderate Hepatic Impairment trials with a reported enrollment target. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07343960, a Phase 1 study of Moderate Hepatic Impairment, is actively recruiting participants, sponsored by AstraZeneca.

RECRUITING
Registry status
Phase 1
Development phase
20 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to measure the pharmacokinetics (PK), safety, and tolerability of capivasertib in participants with moderate hepatic impairment and participants with normal hepatic function (as control).

Primary Outcome

To compare the PK (AUCinf) of a single oral dose of capivasertib in participants with moderate hepatic impairment to participants with normal hepatic function.

Interventions

  • DRUG Capivasertib

Study Locations (2)

California

  • Research Site - Rialto

Texas

  • Research Site - San Antonio

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2026-01-06
Est. Completion 2026-07-31
Phase Phase 1
AstraZeneca

1,285 total trials

What NCT07343960 shows while recruiting

NCT07343960 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, roughly in line with the 21-participant average among 4 other Moderate Hepatic Impairment trials with a reported enrollment target.

The record links to 1 condition, with Moderate Hepatic Impairment appearing as the primary indexed condition, and to 1 intervention - of which Capivasertib is the first listed.

NCT07343960 reports a single indexed study location in California, Texas.

Frequently Asked Questions

What is clinical trial NCT07343960 about?

NCT07343960 is a clinical study titled "A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment". The purpose of this study is to measure the pharmacokinetics (PK), safety, and tolerability of capivasertib in participants with moderate hepatic impairment and participants with normal hepatic function (as control).

What is the current status of trial NCT07343960?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2026-01-06. Estimated completion is 2026-07-31.

What conditions does trial NCT07343960 study?

This clinical trial studies the following conditions: Moderate Hepatic Impairment.

What interventions are being tested in trial NCT07343960?

The interventions under investigation include: Capivasertib (DRUG).

Who is sponsoring clinical trial NCT07343960?

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

Where is trial NCT07343960 being conducted?

This trial has 2 study locations across California, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07343960, the US trial registry maintained by the National Library of Medicine. NCT07343960 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.