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cdk2 inhibitor incb123667

Generic: CDK2 Inhibitor INCB123667

cdk2 inhibitor incb123667: 7 clinical trials tracked.

cdk2 inhibitor incb123667 evidence translation

What we can confirm

7 tracked trials

No verified listed company relationship

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 Trial Registry Records (7)

A Phase 3, Double-Blind, Randomized, Controlled Study of INCB123667 in Combination With Bevacizumab Versus Bevacizumab Alone as First-Line Maintenance Therapy in Participants With Advanced Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer Overexpressing Cyclin E1 (MAESTRA 3)

NCT07797283Registry updated 2026-10-02·Phase 3·INCY
Not yet recruiting

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

InterventionalRandomizedquadruple590 targetStarted 2026-12Completion 2034-05Incyte Corporation

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

NCT07559396Registry updated 2026-06-16·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

NCT07559474Registry updated 2026-06-16·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

NCT07214779Registry updated 2026-10-09·Phase 3·INCY
Recruiting

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

InterventionalRandomizedopen466 targetStarted 2025-12Completion 2029-05197 sites · Australia, Belgium, Canada, France…Incyte 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

NCT07218744Registry updated 2026-01-07·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)

NCT07023627Registry updated 2026-09-15·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

NCT06909162Registry updated 2026-06-15·Phase 1·INCY
Completed

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

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