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2026/6/8 13:54:04
Major Milestone: Affinity’s Legubicin for Injection Granted FDA Orphan Drug Designation, Ushering in a New Chapter for Soft Tissue Sarcoma Treatment
Corporate
2026/4/24 10:12:12
Affinity Presents Breakthrough Preclinical Data of First-in-Class Dual-Masked CLDN6-CD3 TMEA-TCE at AACR: Potent Anti-Tumor Activity with No Observed CRS Signals
Corporate
2026/4/24 10:01:23
Affinity Presents First-in-Class TME-Activated IL-2 Platform (TMEABody) and Clinical Data at AACR, Addressing the Toxicity Challenge of Traditional IL-2 Therapies
Corporate
2026/4/23 9:59:12
Affinity Unveils World’s First Dual-Payload ADC Breakthrough Offering Novel Solutions for RAS-Mutant Tumors and ADC Resistance
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2026/6/8 13:54:04
Major Milestone: Affinity’s Legubicin for Injection Granted FDA Orphan Drug Designation, Ushering in a New Chapter for Soft Tissue Sarcoma Treatment
2026/4/24 10:12:12
Affinity Presents Breakthrough Preclinical Data of First-in-Class Dual-Masked CLDN6-CD3 TMEA-TCE at AACR: Potent Anti-Tumor Activity with No Observed CRS Signals
2026/4/24 10:01:23
Affinity Presents First-in-Class TME-Activated IL-2 Platform (TMEABody) and Clinical Data at AACR, Addressing the Toxicity Challenge of Traditional IL-2 Therapies
2026/4/23 9:59:12
Affinity Unveils World’s First Dual-Payload ADC Breakthrough Offering Novel Solutions for RAS-Mutant Tumors and ADC Resistance
2026/3/21 14:18:58
Affinity to Present Latest Preclinical Research Findings at AACR 2026 Annual Meeting
2025/10/20 9:10:50
Legubicin Phase III Registration Data Selected as LBA for ESMO 2025, with First-Time Data Disclosure in Oral Presentation
2025/3/27 9:09:12
Affinity to Present Research Findings at AACR Annual Meeting 2025
2022/8/9 11:19:32
Affinity’s QHL-236 (Legutaxel) Program Receives Clinical Trial Approval in Australia
2022/4/20 14:59:47
Affinity’s QHL-236 (Legutaxel) Clinical Trial Application Receives Implicit Approval
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