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Akeso Announces Completion of Patient Enrollment in The Phase III Clinical Trial of Cadonilimab for Adjuvant Treatment of High-Risk Recurrent Hepatocellular Carcinoma

  • Akeso announced the completion of patient enrollment for its Phase III clinical trial of cadonilimab, a bispecific antibody for high-risk recurrent hepatocellular carcinoma .
  • Cadonilimab is the world's first PD-1/CTLA-4 bispecific antibody developed by Akeso for HCC, which has a high recurrence rate after surgery.
  • Research at the 2023 ESMO meetings showed cadonilimab's effectiveness, achieving a 100% disease control rate in neoadjuvant therapy for resectable multinodular HCC.
  • Akeso is committed to further advancing cadonilimab's clinical development and currently has over 23 clinical studies in progress across multiple cancer types, aiming to improve patient outcomes worldwide.
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The Laconia Daily SunThe Laconia Daily Sun
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Akeso Announces Completion of Patient Enrollment in The Phase III Clinical Trial of Cadonilimab for Adjuvant Treatment of High-Risk Recurrent Hepatocellular Carcinoma

HONG KONG, March 5, 2025 /PRNewswire/ -- Akeso, Inc. (9926. HK) ("Akeso" or the "Company") is pleased to announce the completion of patient enrollment for its Phase III registrational clinical trial (COMPASSION-22/AK104-306) evaluating cadonilimab, the world's first PD-1/CTLA-4 bispecific antibody…

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Charleston Gazette-Mail broke the news in Charleston, United States on Thursday, March 6, 2025.
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