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ACTIVE NOT RECRUITING
NCT06084416
PHASE1

A Study of Sovilnesib in Subjects With Ovarian Cancer

Sponsor: Volastra Therapeutics, Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

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