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A Study of Sovilnesib in Subjects With Ovarian Cancer
Sponsor: Volastra Therapeutics, Inc.
Summary
This is a randomized, phase 1b study to assess the safety, tolerability, pharmacokinetics (PK), and efficacy of sovilnesib at different dose levels to establish the Recommended Phase 2 Dose (RP2D) of sovilnesib in subjects with high grade serous ovarian cancer (HGSOC).
Official title: A Phase 1b Dose Optimization Study of Sovilnesib (an Oral KIF18A Inhibitor) in Subjects With Advanced High Grade Serous Ovarian Cancer
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
120
Start Date
2024-04-04
Completion Date
2026-04
Last Updated
2025-10-20
Healthy Volunteers
No
Conditions
Interventions
Sovilnesib
Sovilnesib tablets will be given orally.
Locations (13)
The University of Alabama at Birmingham
Birmingham, Alabama, United States
University of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
UCLA
Los Angeles, California, United States
Hoag Memorial Hospital
Newport Beach, California, United States
Georgia Cancer Center Augusta University
Atlanta, Georgia, United States
Johns Hopkins Hospital
Baltimore, Maryland, United States
Dana Farber Cancer Institute
Boston, Massachusetts, United States
Corewell Health
Grand Rapids, Michigan, United States
Roswell Park Comprehensive Cancer Center
Buffalo, New York, United States
Icahn School of Medicine at Mount Sinai
New York, New York, United States
OU Health Stephenson Cancer Center
Oklahoma City, Oklahoma, United States
MUSC Hollings Cancer Center
Charleston, South Carolina, United States
Fred Hutchinson Cancer Center
Seattle, Washington, United States