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Articles published by Daiichi Sankyo

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ENHERTU® Granted Breakthrough Therapy Designation in U.S. for Certain Patients with HER2 Low or HER2 Ultralow Metastatic Breast Cancer

August 19, 2024

From Daiichi Sankyo

Via Business Wire

Daiichi Sankyo and Merck Enter into Global Development and Commercialization Agreement for MK-6070

August 06, 2024

From Daiichi Sankyo

Via Business Wire

Tickers MRK

IDeate-Lung02 Phase 3 Trial of Ifinatamab Deruxtecan Initiated in Patients with Relapsed Small Cell Lung Cancer

August 01, 2024

From Daiichi Sankyo

Via Business Wire

Tickers MRK

Patritumab Deruxtecan BLA Submission Receives Complete Response Letter from FDA Due to Inspection Findings at Third-Party Manufacturer

June 26, 2024

From Daiichi Sankyo

Via Business Wire

Tickers MRK

Datopotamab Deruxtecan Showed Clinically Meaningful Overall Survival Improvement Versus Chemotherapy in Patients with Advanced Nonsquamous Non-Small Cell Lung Cancer in TROPION-Lung01 Phase 3 Trial

May 27, 2024

From Daiichi Sankyo

Via Business Wire

Daiichi Sankyo Highlights Progress in Creating New Standards of Care for Patients Across Multiple Cancers at ASCO

May 21, 2024

From Daiichi Sankyo

Via Business Wire

ENHERTU® Demonstrated Statistically Significant and Clinically Meaningful Improvement in Progression-Free Survival in HR Positive, HER2 Low Metastatic Breast Cancer Following One or More Lines of Endocrine Therapy in DESTINY-Breast06 Phase 3 Trial

April 29, 2024

From Daiichi Sankyo

Via Business Wire

ENHERTU® Approved in the U.S. as First Tumor Agnostic HER2 Directed Therapy for Previously Treated Patients with Metastatic HER2 Positive Solid Tumors

April 05, 2024

From Daiichi Sankyo

Via Business Wire

Tickers AZN

REJOICE-Ovarian01 Phase 2/3 Trial of Raludotatug Deruxtecan Initiated in Patients with Platinum-Resistant Ovarian Cancer

April 03, 2024

From Daiichi Sankyo

Via Business Wire

Tickers MRK

ENHERTU® Granted Priority Review in the U.S. for Patients with Metastatic HER2 Positive Solid Tumors

January 29, 2024

From Daiichi Sankyo

Via Business Wire

Patritumab Deruxtecan Granted Priority Review in the U.S. for Certain Patients with Previously Treated Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer

December 22, 2023

From Daiichi Sankyo

Via Business Wire

Tickers MRK

Two Phase 3 Trials of Datopotamab Deruxtecan Plus Durvalumab Initiated in Patients Across Two Breast Cancer Subtypes

December 18, 2023

From Daiichi Sankyo

Via Business Wire

Daiichi Sankyo Demonstrates Breadth and Depth of Oncology Portfolio Across Multiple Cancers with New Data at ESMO Asia, SABCS and ASH

December 01, 2023

From Daiichi Sankyo

Via Business Wire

ENHERTU® Demonstrated Clinically Meaningful Survival Across Multiple HER2 Expressing Advanced Solid Tumors in DESTINY-PanTumor02 Phase 2 Trial

October 23, 2023

From Daiichi Sankyo

Via Business Wire

Datopotamab Deruxtecan Improved Progression-Free Survival Versus Chemotherapy in Patients with Previously Treated Non-Small Cell Lung Cancer in TROPION-Lung01 Phase 3 Trial

October 23, 2023

From Daiichi Sankyo

Via Business Wire

Datopotamab Deruxtecan Significantly Extended Progression-Free Survival Versus Chemotherapy in Patients with HR Positive, HER2 Low or Negative Breast Cancer in TROPION-Breast01 Phase 3 Trial

October 23, 2023

From Daiichi Sankyo

Via Business Wire

Datopotamab Deruxtecan Plus Durvalumab Demonstrated Robust and Durable Tumor Responses in First-Line Treatment of Patients with Metastatic Triple Negative Breast Cancer in BEGONIA Phase 1b/2 Trial

October 22, 2023

From Daiichi Sankyo

Via Business Wire

Daiichi Sankyo and Merck Announce Global Development and Commercialization Collaboration for Three Daiichi Sankyo DXd ADCs

October 19, 2023

From Daiichi Sankyo

Via Business Wire

Tickers MRK

Daiichi Sankyo Showcases Progress in Developing New Standards of Care for Patients with Industry-Leading DXd ADC Portfolio Across Multiple Cancers at ESMO

October 16, 2023

From Daiichi Sankyo

Via Business Wire

Datopotamab Deruxtecan Demonstrated Statistically Significant and Clinically Meaningful Progression-Free Survival Benefit in Patients with HR Positive, HER2 Low or Negative Breast Cancer in TROPION-Breast01 Phase 3 Trial

September 22, 2023

From Daiichi Sankyo

Via Business Wire

ENHERTU® Demonstrated Strong and Durable Tumor Responses in Previously Treated HER2 Mutant Advanced Lung Cancer in DESTINY-Lung02 Phase 2 Trial

September 11, 2023

From Daiichi Sankyo

Via Business Wire

Datopotamab Deruxtecan Plus Durvalumab Showed Promising Clinical Activity in the First-Line Advanced Non-Small Cell Lung Cancer Setting in TROPION-Lung04 Phase 1b Trial

September 10, 2023

From Daiichi Sankyo

Via Business Wire

Ifinatamab Deruxtecan Continues to Demonstrate Durable Responses in Patients with Advanced Small Cell Lung Cancer in Early Trial

September 10, 2023

From Daiichi Sankyo

Via Business Wire

Patritumab Deruxtecan Demonstrated Clinically Meaningful and Durable Responses in Patients with EGFR-Mutated Metastatic Non-Small Cell Lung Cancer in HERTHENA-Lung01 Phase 2 Trial

September 10, 2023

From Daiichi Sankyo

Via Business Wire

DS-3939 Enters Clinical Development in Patients Across Several Types of Advanced Solid Cancers

September 07, 2023

From Daiichi Sankyo

Via Business Wire

ENHERTU® Granted Two Breakthrough Therapy Designations in U.S. for Patients Across Multiple HER2 Expressing Cancers

August 31, 2023

From Daiichi Sankyo

Via Business Wire

Daiichi Sankyo Highlights Progress in Creating New Standards of Care for Patients with Lung Cancer with Data Across DXd ADC Portfolio at WCLC

August 16, 2023

From Daiichi Sankyo

Via Business Wire

VANFLYTA® Now Available in U.S. for Patients with Newly Diagnosed FLT3-ITD Positive AML

August 09, 2023

From Daiichi Sankyo

Via Business Wire

ENHERTU® Demonstrated Clinically Meaningful Progression-Free Survival and Overall Survival Across Multiple HER2 Expressing Advanced Solid Tumors in DESTINY-PanTumor02 Phase 2 Trial

July 27, 2023

From Daiichi Sankyo

Via Business Wire

VANFLYTA® First FLT3 Inhibitor Approved in the U.S. Specifically for Patients with Newly Diagnosed FLT3-ITD Positive AML

July 20, 2023

From Daiichi Sankyo

Via Business Wire

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