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RECRUITING
NCT06515613
PHASE1

A Phase 1 Study of CTIM-76 in Patients With Recurring Ovarian Cancer and Other Advanced Solid Tumors

Sponsor: Context Therapeutics Inc.

View on ClinicalTrials.gov

Summary

This is a Phase 1a/1b, open-label, dose escalation and expansion study to evaluate the safety and efficacy of CTIM-76 (study drug), a CLDN6-directed T cell-engaging bispecific antibody, in participants with platinum-refractory/resistant ovarian cancer (PRROC) and other advanced CLDN6-positive solid tumors (i.e., testicular and endometrial).

Official title: A Phase 1, First in Human Study of CTIM-76, a Claudin-6 (CLDN6)-Directed Bispecific Antibody, in Patients With Recurring Ovarian Cancer and Other Advanced Solid Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-07-10

Completion Date

2028-04-30

Last Updated

2026-02-20

Healthy Volunteers

No

Interventions

DRUG

CTIM-76

CLDN6 bispecific Antibody administered weekly (Day 1, 8, 15 and 22) of a 28-day treatment cycle until disease progression.

Locations (13)

University of Arkansas Winthrop P. Rockefeller Cancer Institute

Little Rock, Arkansas, United States

Precision NextGen Oncology & Research Center

Beverly Hills, California, United States

SCRI at Denver Health

Denver, Colorado, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

John Theurer Cancer Center

Hackensack, New Jersey, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Duke Cancer Institute

Durham, North Carolina, United States

Gabrail Cancer Center

Canton, Ohio, United States

Providence Cancer Institute of Oregon

Portland, Oregon, United States

Fox Chase Cancer Center

Philadelphia, Pennsylvania, United States

Women & Infants Hospital of Rhode Island

Providence, Rhode Island, United States

Vanderbilt-Ingram Cancer Center

Nashville, Tennessee, United States

SCRI at Mary Crowley

Dallas, Texas, United States