From April 17 to 22, 2026 local time, the 117th Annual Meeting of the American Association for Cancer Research (AACR) was held at the San Diego Convention Center in the United States. Keyisheng Pharma, a controlled subsidiary of 3D Medicines Inc. (Stock Code: 1244.HK) focusing on innovative radiopharmaceutical R&D, unveiled for the first time the preclinical and preliminary clinical data of its independently developed PSMA-targeted radiopharmaceutical drug conjugate (RDC), ¹⁷⁷Lu-PSMA-3D1015 (hereinafter referred to as “3D1015s”).
Shanghai, China – On October 23, 2025, 3D Medicines (1244.HK) announced the successful completion of follow-up for the first patient enrolled in the investigator-initiated trial (IIT) of 3D1015, its core radioligand drug conjugate (RDC) candidate.
As one of the world's most influential oncology conferences, the European Society for Medical Oncology (ESMO) has long been dedicated to advancing global efforts in cancer research and treatment. The ESMO Congress 2025 was successfully held in Berlin, Germany, from October 17 to 21, 2025 (local time), in a hybrid format combining in-person and virtual participation. The congress showcased a wealth of cutting-edge clinical research findings and brought together leading international experts to discuss emerging trends in oncology therapeutics and patient management. Notably, multiple studies on Envafolimab® (Envafolimab Injection) were selected for presentation, highlighting its growing scientific and clinical impact.
February 8th, 2025, Shanghai, China—3D Medicines Inc. (1244.HK) today announced the appointment of Mr. Gan Ding as Chief Commercial Officer (CCO). With three decades of experience in the biopharmaceutical industry across China, the United States, and internationally, Mr. Ding brings a wealth of expertise that will drive the future commercial development of 3D Medicines.
With the widespread clinical application of the subcutaneous injection of PD-L1 antibody drug 恩维达® (Envafolimab)in tumor treatment, good news of i...
VOLUNTARY ANNOUNCEMENT APPROVAL FROM FDA TO PROCEED WITH A GLOBAL PHASE III TRIAL FOR TREATMENT OF THE FIRST LINE MISMATCH REPAIR PROFICIENT (pMMR) ADVANCED OR RECURRENT ENDOMETRIAL CANCER