BioNTech, OncoC4 On Saturday, Announced Clinically Meaningful Overall Survival Benefit For Selective Treg Modulator Gotistobart In Patients With Previously Treated Squamous Non-Small Cell Lung Cancer

BioNTech SE (NASDAQ:BNTX, "BioNTech")) and OncoC4, Inc. ("OncoC4") presented data from the non-pivotal dose-confirmation stage of the global randomized Phase 3 trial PRESERVE-003 (NCT05671510) for gotistobart (also known as BNT316 or ONC-392), a tumor microenvironment-selective regulatory T cell ("Treg") depletion candidate, targeting CTLA-4 in patients with metastatic squamous non-small cell lung cancer (sqNSCLC). Gotistobart demonstrated a clinically meaningful overall survival ("OS") benefit compared to standard-of-care chemotherapy and a manageable safety profile in sqNSCLC patients whose disease had progressed following anti-PD-(L)1 therapy and platinum-based chemotherapy. Data from the non-pivotal stage of the trial are being presented today in an oral presentation at the IASLC ASCO 2025 North America Conference on Lung Cancer, hosted by the International Association for the Study of Lung Cancer in Chicago, Illinois, USA.

• (BNT316/ONC-392) showed a reduction in the risk of death by more than half compared to standard of care chemotherapy and a manageable safety profile in the first of two stages of the global Phase 3 trial PRESERVE-003 in patients with squamous non-small cell lung cancer ("sqNSCLC") who have progressed on prior immunotherapy plus chemotherapy
• Median OS with gotistobart has not been reached at almost 15 months of follow-up, compared to a median OS of 10 months observed with chemotherapy
• As a chemotherapy-free monotherapy, gotistobart has the potential to become an alternative to traditional cytotoxic treatment for a patient population with high unmet medical need
• Gotistobart was granted Fast Track Designation by the U.S. Food and Drug Administration ("FDA") for the treatment of patients with metastatic NSCLC whose disease progressed on prior anti-PD-(L)1 therapy