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Taking people in United StatesPhase 1

Tests CTIM-76 in adults with recurring ovarian cancer and other solid tumors

Tests CTIM-76 in adults with advanced ovarian, testicular or endometrial cancer.

Plain-language title generated from the registry record
Registry title: A Phase 1 Study of CTIM-76 in Patients With Recurring Ovarian Cancer and Other Advanced Solid Tumors

Key facts

Where
Beverly Hills, Boston, Canton, Dallas, Denver, Durham, Hackensack, Little Rock, Nashville, New York, Omaha, Philadelphia, Portland, and Providence, United StatesSee the 14 sites
Phase
Phase 1

Where in United States

  • Precision NextGen Oncology & Research CenterBeverly Hills, United StatesNo longer taking part
  • Dana-Farber Cancer InstituteBoston, United StatesTaking people
  • Gabrail Cancer CenterCanton, United StatesNo longer taking part
  • SCRI at Mary CrowleyDallas, United StatesTaking people
  • SCRI at Denver HealthDenver, United StatesTaking people
  • Duke Cancer InstituteDurham, United StatesTaking people
  • John Theurer Cancer CenterHackensack, United StatesNo longer taking part
  • University of Arkansas - Winthrop P. Rockefeller Cancer InstituteLittle Rock, United StatesTaking people
  • Vanderbilt-Ingram Cancer CenterNashville, United StatesTaking people
  • Memorial Sloan-Kettering Cancer CenterNew York, United StatesTaking people
  • University of Nebraska MedicalOmaha, United StatesTaking people
  • Fox Chase Cancer CenterPhiladelphia, United StatesNo longer taking part
  • Providence Cancer Institute of OregonPortland, United StatesTaking people
  • Women & Infants Hospital of Rhode IslandProvidence, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Context Therapeutics Inc.
Trial code
NCT06515613EU 2025-523968-20-00
Record updated
10 November 2026
Original description
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).Read full original descriptionShow less

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

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).

Inclusion: Participants with CLDN6 positive platinum resistant/refractory ovarian, advanced testicular or advanced endometrial cancer; Participants with measurable disease per RECIST 1.1; ECOG 0, 1, or 2 and life expectancy of ≥ 12 weeks; Participants with adequate organ function.

Exclusion: Concurrent participation in another investigational clinical trial; Evidence of central nervous system metastases, leptomeningeal disease or spinal cord compression; Uncontrolled significant active infection or any medical or other condition that in opinion of the Investigator would preclude the participant's participation in the study.

ClinicalTrials.gov NCT06515613 · EU CTIS 2025-523968-20-00