Study to Evaluate INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
Part of paid clinical trials in Anchorage, Alaska.
- Sponsor
- Incyte Corporation
- Study ID
- NCT07214779
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- INCB123667 — DRUGOral; tablet
- Investigator's choice of chemotherapy — DRUGThe investigator will select the chemotherapy in accordance with the protocol-defined requirements. The possible choices as defined by the protocol:
Study Details
The purpose of this study is to evaluate INCB123667 versus investigator's choice of chemotherapy in participants with platinum-resistant ovarian cancer with cyclin E1 overexpression.
Key Dates
- Start date
- Dec 9, 2025
- Status verified
- May 2026
- Primary completion
- Nov 15, 2028
- Completion
- May 14, 2029
Study Design
- Enrollment
- 466 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment Group A (TGA)INCB123667 at the protocol-defined dose.
- Experimental: Treatment Group B (TGB)Investigator's choice of chemotherapy at the protocol-defined dose as defined by the protocol.
Primary Outcome Measure
Progression-Free Survival (PFS) by BICR [ Time Frame: Up to 2 years ]
Central Contacts
- Incyte Corporation Call Center (US)1.855.463.3463
- Incyte Corporation Call Center (ex-US)+800 00027423
Locations (29)
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