Highlights

05/03 Akeso, Inc. Presents Long-Term Phase II Results For Cadonilimab In Recurrent Or Metastatic Cervical Cancer CI
04/03 INOVIO and Akeso Enter Clinical Collaboration to Advance Novel Combination Therapy for Glioblastoma CI
11/02 Akeso, Inc.'s IL-4Ra/ST2 Bispecific Antibody Cleared for Seven Phase II Studies in China Spanning Respiratory and Autoimmune Indications CI
06/02 Akeso, Inc. Receives Fifth Breakthrough Therapy Designation from NMPA for Ivonescimab in First-Line Treatment of Advanced Biliary Tract Cancer CI
03/02 Akeso granted exclusive commercialization rights for ebronucimab injection to Jumpcan Pharmaceutical RE
03/02 Akeso Grants Commercialization Rights for Hypercholesterolemia Drug to Hubei Jumpcan Pharmaceutical Unit MT
29/01 Summit Therapeutics Announces U.S. FDA Acceptance of Biologics License Application Seeking Approval for Ivonescimab in Combination with Chemotherapy in Treatment of Patients with EGFRm NSCLC Post-TKI Therapy CI
19/01 Akeso, Inc. Announces NMPA Acceptance of Second NDA for Gumokimab (IL-17A Inhibitor) in Active Ankylosing Spondylitis CI
14/01 Akeso, Inc. Announces Presentation of Real-World Study At the 2026 American Society of Clinical Oncology Gastrointestinal Cancers Symposium CI
13/01 Summit Therapeutics Inc. Announces Submission of Biologics License Application to U.S. FDA Seeking Approval for Ivonescimab in Combination with Chemotherapy in 2L+ Treatment of Patients with EGFRm NSCLC CI
07/01 Akeso, Inc. Announces the National Medical Products Administration Approves Significant Label Update in China for its Internally Develop, PD-1/VEGF Bispecific Antibody, ivonescimab CI
12/12 Cadonilimab (PD-1/CTLA-4) Receives FDA Clearance for Global Phase III First-Line Gastric Cancer Trial Versus Nivolumab CI
11/12 Akeso, Inc. Announces Updated Efficacy Data of Ivonescimab Combined with Chemotherapy as First-Line Treatment for TNBC Presented atESMO IO 2025 CI
09/12 Akeso, Inc. Announces Phase II Data of Cadonilimab Regimen as Neoadjuvant Therapy for Resectable Gastric Cancer Presented at ESMO Asia Congress CI
09/12 Akeso, Inc. Announces Significant Improvement in Quality of Life Reported in Updated HARMONi-6 Data for Ivonescimab at ESMO Asia CI
17/11 Akeso, Inc.'s Bispecific Antibody Targeting Aß and BBB-Expressed Receptor Approved for Alzheimer's Disease Clinical Trials in China CI
10/11 Akeso Announces First Patient Dosed in Phase I Trial of Personalized mRNA Vaccine AK154 as Monotherapy or in Combination with Cadonilimab or Ivonescimab for Adjuvant Treatment of Pancreatic Cancer CI
07/11 Akeso, Inc. Unveils Promising Preclinical Data for IL-1RAP Targeting Antibody At SITC 2025 CI
07/11 Akeso Announces Final OS Analysis Results Of Ivonescimab HARMONi-A Study At SITC 2025 CI
03/11 Akeso's Ivonescimab Secures Fourth Breakthrough Therapy Designation in China for First-Line Treatment of Triple-Negative Breast Cancer CI
31/25/31 Summit Therapeutics Inc. Announces Results from the Phase III Harmoni-A Trial, Conducted in China and Sponsored by Akeso, Inc CI
19/25/19 Akeso Announces Results of the Registrational Phase III Clinical Study Evaluating Ivonescimab (PD-1/VEGF Bispecific Antibody) CI
19/25/19 Summit Intends to Open Clinical Trial Sites in the United States for the Phase Iii Harmoni-Gi3 Study in Colorectal Cancer by the End of 2025 CI
16/25/16 HARMONi-6 Phase III Study of Ivonescimab Accepted by the Lancet and Selected for ESM0 2025 LBA Presentation CI
23/25/23 Akeso Inc. Announces Late-Breaking abstract from the Registrational Phase III Clinical Study (AK-306/HARMONi-6 Study) of Ivonescimab CI
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