Niraparib in High-grade Endometrial Cancer Trial
- Sponsor
- Sir Mortimer B. Davis - Jewish General Hospital
- Study ID
- NCT05289648
- Phase
- EARLY_PHASE1
- Status
- Withdrawn
Conditions
- Endometrial Cancer
- Serous Adenocarcinoma
- Uterine Neoplasm
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Niraparib oral capsule — DRUGLow dose oral niraparib capsules (2 x 100 mg) once a day for 28 days
Study Details
The study will investigate the effect of niraparib on tumor tissue in chemotherapy naïve, newly diagnosed, high-grade endometrial cancer patients. Biomarkers of cognate molecular pathways as well as investigational assays will be used to study the antineoplastic effect of the drug.
Key Dates
- Start date
- May 1, 2024
- Status verified
- Dec 2024
- Primary completion
- Oct 31, 2025
- Completion
- Jan 31, 2026
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Preoperative NiraparibSingle arm. Following the initial assessment and endometrial biopsy the participants will receive niraparib for 28 days. After the treatment period the patients will be surgically staged. All participants will receive the standard of care.
Primary Outcome Measure
Tumor cells proliferation before and after the treatment [ Time Frame: Day 30 (day of surgery) ]
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