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Clinical Trial Summary

The purpose of this research study is to test the proportion of tumor response to the combination treatment with niraparib and bevacizumab and see what effects (good and bad) this combination treatment has on patients with recurrent endometrial or ovarian cancer with ARID1A mutation.


Clinical Trial Description

Patients will have tests and exams to see if they are eligible for the clinical trial. If found eligible, the patient will be randomized into one of two groups and receive treatment as follows: If patients are in the first group,they will receive niraparib alone, once daily taken by mouth. If patients are in the second group, they will receive niraparib once daily taken by mouth and infusion of bevacizumab once every 3 weeks. Patients will receive the study treatment as long as there is evidence that the tumor is not growing or spreading and they are not having any unacceptable, bad side effects. Patients will be monitored during treatment with tests and exams and after treatment completion for up to 3 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05523440
Study type Interventional
Source University of Oklahoma
Contact SCC IIT Office
Phone 405-271-8777
Email SCC-IIT-Office@ouhsc.edu
Status Recruiting
Phase Phase 2
Start date February 15, 2023
Completion date January 2027

See also
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