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cdk2 inhibitor incb123667

Generic: CDK2 Inhibitor INCB123667

cdk2 inhibitor incb123667: 6 clinical trials tracked.

cdk2 inhibitor incb123667 evidence translation

What we can confirm

6 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about cdk2 inhibitor incb123667, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence5 indications · 1 study sponsors
Clinical Trials (6)

A Phase 1, Open-Label Study to Assess the Safety and Pharmacokinetics of INCB123667 When Administered Orally to Adult Participants With Severe Renal Impairment or End Stage Renal Disease

NCT07559396·Phase 1·INCY
Recruiting

Primary endpoint: PK for plasma INCB123667: Cmax

InterventionalRandomizedopen16 targetStarted 2026-05Completion 2027-012 sites · United StatesIncyte Corporation

A Phase 1, Open-Label Study to Assess the Safety and Pharmacokinetics of INCB123667 When Administered Orally to Adult Participants With Moderate or Severe Hepatic Impairment

NCT07559474·Phase 1·INCY
Recruiting

Primary endpoint: PK for plasma INCB123667: Cmax

InterventionalRandomizedopen16 targetStarted 2026-05Completion 2027-044 sites · United StatesIncyte Corporation

A Phase 3, Randomized, Open-Label Study of INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

NCT07214779·Phase 3·INCY
Recruiting

Primary endpoint: Progression-Free Survival (PFS) by BICR

InterventionalRandomizedopen466 targetStarted 2025-12Completion 2029-0550 sites · Australia, United StatesIncyte Corporation

An Open-Label Study Assessing the Mass Balance, Pharmacokinetics, and Metabolite Profiles of a Single Oral Dose of [14C]-INCB123667 in Healthy Male Participants

NCT07218744·Phase 1·INCY
Completed

Primary endpoint: Total Recovery (Urine + Feces) of the Administered Radioactivity

Interventionalopen9 enrolledStarted 2025-11Completion 2025-121 site · United StatesIncyte Corporation

A Phase 2, Single-Arm Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression (MAESTRA 1)

NCT07023627·Phase 2·INCY
Recruiting

Primary endpoint: Objective Response by IRC

Interventionalopen160 targetStarted 2025-11Completion 2027-1050 sites · Australia, Belgium, Japan, United StatesIncyte Corporation

A Phase 1, Open-Label Study to Evaluate the Effect of Food on the Single-Dose Pharmacokinetics and a Drug-Drug Interaction Evaluation of Itraconazole and Carbamazepine on INCB123667 When Administered Orally to Healthy Adult Participants

NCT06909162·Phase 1·INCY
Completed

Primary endpoint: Pharmacokinetics Parameter (PK): Cmax of INCB123667

InterventionalRandomizedopen51 enrolledStarted 2025-05Completion 2026-051 site · United StatesIncyte Corporation