Study of the Drug Sovilnesib in People with Ovarian Cancer

About the Study

This study will test the safety and effectiveness of the drug sovilnesib in patients with ovarian cancer. The study will be divided into two parts.

Part 1: 10 people will be assigned at random to receive different dose levels of the drug sovilnesib. Sovilnesib is a drug in pill form and is taken by mouth.

Part 2: 20 to 30 people will be assigned at random to receive two or more dose levels of the drug sovilnesib by mouth.

What the Study Involves

People in the study will take sovilnesib orally in 28-day cycles. They will continue to receive the medication until the treatment stops working, causes serious side effects, or they do not wish to continue with the treatment.

Study Sites

California

Newport Beach
Hoag Memorial Hospital
Contact: Patrice Jones at 949-764-5501 or email at Patrice.jones@hoag.org

Maryland

Baltimore
Johns Hopkins Hospital
Contact Johns Hopkins at 410-614-1361 or email at HopkinsGynTrials@jhmi.edu

Massachusetts

Boston
Dana Farber Cancer Institute
Contact Joyce Liu, MD at 877-338-7425

New York

New York
Icahn School of Medicine at Mount Sinai
Contact Neha Kumarley, MPH, CCRC at 212-824-7859 or email at neha.kumarley@mssm.edu

Washington

Seattle
Fred Hutchinson Cancer Center
Contact GynResearch@fredhutch.org

This Study is Open To:

This study is open to females assigned at birth, aged 18 years and older, who meet the following criteria:

Have high-grade serous ovarian, , or primary peritoneal cancer
Have or inoperable cancer
Have platinum resistance (have recurrent cancer within 6 months after platinum therapy) or platinum-refractory ovarian, or primary peritoneal cancer
Had previously bevacizumab therapy or were not eligible for the treatment
People who have an inherited or acquired or mutation must have previously received a or were not eligible for treatment

This Study is Not Open To:

This study is not open to people who:

Are under 18 years old
Male
Have any of the following biomarkers in their tumor: MSI-H, (), or POLE gene mutation
Have endometrioid, clear cell, mucinous, sarcomatoid, low-grade/borderline ovarian tumor, or mixed tumors containing an , (), or POLE gene mutation
Previously received a KIF18A inhibitor
Have diseases in the brain or nervous system
Had myocardial infarction (MI) or stroke within 6 months
Had unstable angina, pulmonary embolism (arteries in the lungs are blocked by a blood clot), or deep vein thrombosis (formation of a blood clot in a deep vein) within 6 months
Had coronary artery bypass surgery within 6 months
Have any gastrointestinal condition that might affect the absorption of oral medications