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Featured Image: General views at the American Society for Clinical Oncology (ASCO) annual meeting. Courtesy: © ASCO/Max Gersh 2015. Used with permission.

Advances, Sequencing Challenges, and Real-World Integration of ADCs in Breast Cancer:...

Advances, Sequencing Challenges, and Real-World Integration of ADCs in Breast Cancer: Insights from ASCO 2026
Daiichi Sankyo

Datopotamab deruxtecan: First TROP2-Directed ADC Approved for First-Line Treatment of mTNBC...

Datopotamab deruxtecan: First TROP2-Directed ADC Approved for First-Line Treatment of mTNBC in Patients Ineligible for Immunotherapy

AAX Biotech and Daiichi Sankyo to Evaluate Opti-mAb® Technology in Next-Generation...

AAX Biotech, founded by experts from Karolinska Institutet in Stockholm, Sweden, and Daiichi Sankyo are collaborating in the evaluation of  AAX Biotech's Opti-mAb®technology. AAX Biotech pioneers...

Daiichi Sankyo and Merck & Co/MSD Voluntarily Withdraw Biologics License Application...

Daiichi Sankyo and Merck & CO/MSD have voluntarily withdrawn the Biologics License Application (BLA) seeking accelerated approval in the U.S. for patritumab deruxtecan (HER3-DXd) in patients with previously treated locally advanced or metastatic EGFR-mutated Non-Small Cell Lung Cancer (NSCLC) previously treated with two or more systemic therapies.

Phase 3 TROPION-Lung12 Study Evaluates Datopotamab Deruxtecan as Part of Adjuvant...

A first patient has been dosed in the TROPION-Lung12 phase 3 trial (NCT06564844), a global, multicenter, three-arm, open-label phase 3 trial designed to evaluate the efficacy and safety of adjuvant datopotamab deruxtecan (6 mg/kg; Datroway®; Daiichi Sankyo and AstraZeneca; see: ADC Drug Map) in combination with the PD-1/TIGIT bi-specific antibody rilvegostomig* (750 mg) or rilvegostomig monotherapy (750 mg) monotherapy versus observation or standard of care adjuvant chemotherapy regimens.
Daiichi Sankyo

Daiichi Sankyo to Invests US $152M in New ADC Manufacturing Plant...

Japanese drugmaker Daiichi Sankyo this week confirmed that the company will invest approximately US $ 152 million (RMB 1.1 billion) in the construction of a new manufacturing facility for antibody-drug conjugate (ADC-) production in Zhangjiang, Shanghai.

Gilles Gallant, BPharm, PhD, FOPQ, Receives the 2022 George R. Pettit...

Gilles Gallant, BPharm, Ph.D., FOPQ, Chief Development Officer, at Mythic Therapeutics has received the George R. Pettit Individual Input to the Field Award for 2022.  The award was presented at the 13th World ADC Conference, held in San Diego, CA, during the 9th World ADC Awards Ceremony held on Thursday, September 8, 2022.

US FDA Approves Trastuzumab Deruxtecan for the treatment of HER2-Mutant NSCLC

The United States Food and Drug Administration (FDA) has approved trastuzumab deruxtecan* (Enhertu®; Daiichi Sankyo and AstraZeneca) for the treatment of adult patients with...

Trastuzumab deruxtecan Doubles Progression-Free Survival in Metastatic Breast Cancer with Low...

The use of trastuzumab deruxtecan (Enhertu®; Daiichi Sankyo and AstraZeneca), a new HER2-targeting antibody-drug conjugate, doubled progression-free survival (PFS) compared to standard-of-care treatment with...

The Rise of HER2-targeting ADCs and the Journey from Breakthrough Therapy...

Antibody-drug conjugates (ADCs) as precision targeted cancer therapies have started to deliver on their early promise as an innovative novel drug modality as demonstrated...