A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
Part of paid clinical trials in Mobile, Alabama.
- Sponsor
- Incyte Corporation
- Study ID
- NCT07023627
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Not accepted
Interventions
- INCB123667 — DRUGAdministered orally twice daily (BID).
Study Details
This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.
Key Dates
- Start date
- Nov 12, 2025
- Status verified
- May 2026
- Primary completion
- Apr 27, 2027
- Completion
- Oct 24, 2027
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort 1INCB123667 will be administered at the protocol defined dose based on their tumor cyclin E1 expression levels as defined in the protocol.
- Experimental: Cohort 2INCB123667 will be administered at the protocol defined dose based on their tumor cyclin E1 expression levels as defined in the protocol.
- Experimental: Cohort 3INCB123667 will be administered at the protocol defined dose based on their tumor cyclin E1 expression levels as defined in the protocol.
Primary Outcome Measure
Objective Response by IRC [ 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 (42)
Find similar trials in Mobile, AL
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By research site
Usa Health Mitchell Cancer Institute· Mobile, ALUniversity of California, Los Angeles Medical Center· Los Angeles, CAScripps Healthscripps Mercy Hospital Prebys Cancer Center· San Diego, CAMedstar Georgetown University Hospital· Washington D.C., DCFlorida Cancer Specialists & Research Institute· Fort Myers, FLSylvester Comprehensive Cancer Center· Miami, FL
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