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NCT05976321

A Study of TAK-279 in Adults With or Without Liver Damage

Completed Phase 1 Last updated 29 August 2024
What this trial tests

Phase 1 trial testing TAK-279 in Hepatic Impairment in 27 participants. Completed in 15 April 2024.

Timeline
22 September 2023
Primary endpoint
15 April 2024
15 April 2024

Quick facts

Lead sponsorTakeda
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposebasic science
Enrollment27
Start date22 September 2023
Primary completion15 April 2024
Estimated completion15 April 2024
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Takeda — full company profile →

Who can join

18 and older, any sex, with Hepatic Impairment or Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main aim of this study is to find out how the body processes 1 dose of TAK-279 (pharmacokinetics) in participants with liver problems compared to participants without liver problems. Other aims are to check for side effects from TAK-279 and to learn how well participants tolerate 1 dose of TAK-279. The participants will need to stay at the clinic for 11 days.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of TAK-279

Trials testing the same drug.

Other recruiting trials for Hepatic Impairment

Currently open trials in the same condition.

Other Takeda trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05976321.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing