2 April 2026 - Context Therapeutics today announced that the US FDA has granted fast track designation to CTIM-76, a CLDN6 x CD3 T cell engaging bispecific antibody, for the treatment of platinum-resistant ovarian cancer in patients that have received all standard of care therapies.
Context is currently evaluating CTIM-76 in a Phase 1 clinical trial designed to evaluate the safety and efficacy of CTIM-76 in subjects with CLDN6 positive advanced or metastatic ovarian, endometrial and testicular cancers.