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Innovent Presents Updated IBI363 Data in Colorectal Cancer at ASCO 2025

  • Innovent Biologics presented Phase 1 and 2 data of IBI363 for immunotherapy-pretreated melanoma at the 2025 ASCO Annual Meeting on June 1, 2025, from San Francisco and Suzhou, China.
  • The data followed extensive clinical studies targeting treatment-resistant cold tumors, including acral and mucosal melanoma, which have limited efficacy with current treatments and represent a significant unmet need in China.
  • In 31 heavily treated patients dosed at 1 mg/kg biweekly, IBI363 achieved a 23.3% confirmed objective response rate and a 76.7% disease control rate, with durable responses lasting a median of 14.0 months and median progression-free survival of 5.7 months.
  • The median overall survival reached 14.8 months overall and 19.3 months for mucosal melanoma, while treatment-related adverse events were mostly mild, with manageable safety and only 3.2% discontinuations due to adverse effects.
  • A pivotal randomized Phase 2 trial comparing IBI363 to pembrolizumab in untreated mucosal and acral melanoma started dosing in March 2025, aiming to establish IBI363 as a new immunotherapy standard for these cold tumor subtypes.
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ASCO 2025 Oral Presentation: Innovent Biologics Announces Updated Data of IBI363 (First-in-class PD-1/IL-2α -bias Bispecific Antibody Fusion Protein) from Phase 1 and 2 Clinical Studies on Immunotherapy-treated Advanced Malignant Melanoma

SAN FRANCISCO and SUZHOU, China, June 1, 2025 /PRNewswire/ -- Innovent Biologics, Inc (Suzhou) (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high-quality medicines for the treatment of oncology, cardiovascular and metabolic, autoimmune, ophthalmology and other major…

·Helena, United States
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The Billings Gazette broke the news in Billings, United States on Sunday, June 1, 2025.
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