A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

Sponsor: Incyte Corporation

Sponsor score: 60

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

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

  • Histological diagnosis of a high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer.

  • 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.
  • 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.

  • 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.

  • Must have received bevacizumab unless there was a contraindication for its use.

  • 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

FACILITYZIPCITYSTATE
Usa Health Mitchell Cancer Institute36604MobileAlabama
Uams Winthrop P Rockefeller Cancer Institute72205Little RockArkansas
University of California, Los Angeles Medical Center90024-6995Los AngelesCalifornia
Scripps Healthscripps Mercy Hospital Prebys Cancer Center92103San DiegoCalifornia
Medstar Georgetown University Hospital20010Washington D.C.District of Columbia
Florida Cancer Specialists & Research Institute33901Fort MyersFlorida
Mayo Clinic32224JacksonvilleFlorida
Sylvester Comprehensive Cancer Center33136MiamiFlorida
Mount Sinai Comprehensive Cancer Center33140Miami BeachFlorida
Florida Cancer Specialists & Research Institute33401West Palm BeachFlorida

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