A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
Sponsor: Incyte Corporation
ClinicalTrials ID:NCT07023627
This clinical trial assesses the safety and efficacy of INCB123667, an oral drug taken twice daily, in patients with platinum-resistant ovarian cancer exhibiting Cyclin E1 overexpression. Eligible participants must have high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer, meet specific treatment history criteria, and be willing to undergo a pretreatment biopsy.
Patient Parameters
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Program Overview
This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.
Eligibility Criteria
Inclusion Criteria
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Histological diagnosis of a high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer.
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Have platinum-resistant disease:
- Participants who have only had 1 line of platinum-based therapy must have received at least 4 cycles of a platinum-containing regimen.
- Participants who have received 2 to 4 lines of platinum-based therapy must have progressed on or within 6 months after the last dose of platinum.
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Willingness to undergo a pretreatment biopsy. Note: Tissue from a fresh pretreatment biopsy is preferred, however an archival sample is acceptable as long as the sample is no older than 5 years.
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Received at least 1 and no more than 4 prior lines of systemic therapy following the initial diagnosis, after which single-agent therapy is considered an appropriate next therapeutic option.
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Must have received bevacizumab unless there was a contraindication for its use.
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If the tumor tests positive for FRα, participants must have received mirvetuximab soravtansine unless there is an exception for its use on medical grounds.
Exclusion Criteria
- Have endometrioid, clear cell, mucinous, or sarcomatous histology, mixed tumors containing any of these histologies, or low-grade/borderline ovarian cancer.
- Have primary platinum-refractory disease: either did not respond (CR or PR) to first-line platinum-containing therapy or progressed on or within 3 months after the last dose of the first line platinum-containing therapy.
- The tumor tests positive for FRα but the participant has not received mirvetuximab soravtansine for any reason other than medical contraindication.
- Clinically significant or uncontrolled cardiac disease within 6 months before the first dose of study drug.
- Known active CNS metastases and/or carcinomatous meningitis.
- Known additional malignancy that is progressing or requires active treatment.
Other protocol-defined Inclusion/Exclusion Criteria may apply.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Usa Health Mitchell Cancer Institute | 36604 | Mobile | Alabama |
| Uams Winthrop P Rockefeller Cancer Institute | 72205 | Little Rock | Arkansas |
| University of California, Los Angeles Medical Center | 90024-6995 | Los Angeles | California |
| Scripps Healthscripps Mercy Hospital Prebys Cancer Center | 92103 | San Diego | California |
| Medstar Georgetown University Hospital | 20010 | Washington D.C. | District of Columbia |
| Florida Cancer Specialists & Research Institute | 33901 | Fort Myers | Florida |
| Mayo Clinic | 32224 | Jacksonville | Florida |
| Sylvester Comprehensive Cancer Center | 33136 | Miami | Florida |
| Mount Sinai Comprehensive Cancer Center | 33140 | Miami Beach | Florida |
| Florida Cancer Specialists & Research Institute | 33401 | West Palm Beach | Florida |
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