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Phase II Clinical Trial Repurposing Atovaquone for the Treatment of Platinum-Resistant Ovarian Cancer
This phase II trial test tests how well repurposing atovaquone works in treating patients with platinum-resistant ovarian cancer. Atovaquone is used for the treatment or prevention of certain infections. Atovaquone is in a class of medications called antiprotozoal agents. It works by stopping the growth of certain types of protozoa that can cause pneumonia. Giving atovaquone may be effective in treating platinum-resistant ovarian cancer and result in improved outcomes compared to standard chemotherapy regimens.
PRIMARY OBJECTIVE: I. To determine progression free survival of twenty-eight patients with platinum-resistant ovarian cancer treated with atovaquone. SECONDARY OBJECTIVES: I. To determine clinical benefit rate (complete response, partial response or stable disease) at six months. II. To determine overall survival. III. To quantitate the on-target STAT3 inhibitory effect of atovaquone on STAT3-dependent gene transcription. IV. To quantitate changes of the tumor immune infiltrate by inhibition of STAT3 with atovaquone. OUTLINE: Patients receive atovaquone orally (PO) on study. Patients also undergo computed tomography (CT) and biopsy or paracentesis throughout the study. After completion of study treatment, patients are followed up for 30 days and then every 6 month thereafter.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Emory University Hospital/Winship Cancer Institute
Atlanta, Georgia, United States
Start Date
November 9, 2023
Primary Completion Date
June 30, 2026
Completion Date
June 30, 2027
Last Updated
September 11, 2025
28
ESTIMATED participants
Atovaquone
DRUG
Biopsy
PROCEDURE
Computed Tomography
PROCEDURE
Paracentesis
PROCEDURE
Lead Sponsor
Emory University
Collaborators
NCT05039801
NCT01116648
Data Source & Attribution
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