BASKING RIDGE, New Jersey and MUNICH, May 16, 2018
- Updated results from the large ongoing phase 1 study of DS-8201, an investigational HER2-targeting antibody drug conjugate (ADC), in metastatic breast cancer, gastric cancer and other tumors with HER2 as cell surface target to be reported
- First-in-human clinical data from phase 1 study of U3-1402, an investigational and potential first-in-class HER3-targeting ADC, in metastatic breast cancer with HER3 as cell surface target to be presented
- Results from the pivotal phase 3 ENLIVEN study of pexidartinib, the first placebo-controlled trial of a systemic therapy in tenosynovial giant cell tumor (TGCT), to be unveiled
- Data presentations highlight substantial progress of oncology pipeline of Daiichi Sankyo, demonstrating its commitment to translating innovative science into potential new precision medicines for patients with cancer
BASKING RIDGE, New Jersey and MUNICH, May 16, 2018 /PRNewswire/ -- Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) today announced that it will present new data for multiple investigational compounds in the Daiichi Sankyo Cancer Enterprise pipeline at the 2018 American Society of Clinical Oncology (ASCO) Annual Meeting from June 1-5 in Chicago. Key highlights include new results from ongoing phase 1 studies of antibody drug conjugates, DS-8201 and U3-1402, in breast cancer and other tumors, as well as results from the pivotal, phase 3 ENLIVEN study of pexidartinib in tenosynovial giant cell tumor (TGCT), also known as giant cell tumor of the tendon sheath (GCT-TS) and previously referred to as pigmented villonodular synovitis (PVNS), a rare and debilitating tumor of the joint or tendon sheath.
"We are excited to reveal updated results of DS-8201 in patients with heavily pre-treated solid tumors with HER2 as the cell surface target, as well as initial proof-of-concept results for U3-1402, our second smart chemotherapy in development that utilizes our proprietary DXd ADC technology, in HER3 breast cancer," said Antoine Yver, MD, MSc, Executive Vice President and Global Head, Oncology Research and Development, Daiichi Sankyo. "We also will be presenting the pivotal results of pexidartinib, the first systemic therapy examined in a phase 3 study of carefully monitored patients with TGCT, a debilitating and difficult-to-manage non-malignant tumor with treatment options largely limited to surgery. This wealth of data and development candidates showcases our commitment to aligning innovative science with well-characterized disease biology to rapidly develop therapies for patients with cancer."
The following data from the pipeline of Daiichi Sankyo Cancer Enterprise will be presented:
Investigational ADC Franchise Presentations
Investigational Breakthrough Science Presentations
Investigational AML Franchise Presentations
These are investigational agents that have not been approved for any indication in any country. Safety and efficacy of these investigational agents have not been established.
About Daiichi Sankyo Cancer Enterprise
The mission of Daiichi Sankyo Cancer Enterprise is to leverage our world-class, innovative science and push beyond traditional thinking to create meaningful treatments for patients with cancer. We are dedicated to transforming science into value for patients, and this sense of obligation informs everything we do. Anchored by three pillars including our investigational Antibody Drug Conjugate Franchise, Acute Myeloid Leukemia Franchise and Breakthrough Science, we aim to deliver seven distinct new molecular entities over eight years during 2018 to 2025. Our powerful research engines include two laboratories for biologic/immuno-oncology and small molecules in Japan, and Plexxikon Inc., our small molecule structure-guided R&D center in Berkeley, CA. Compounds in pivotal stage development include: DS-8201, an antibody drug conjugate (ADC) for HER2-expressing breast, gastric and other cancers; quizartinib, an oral selective FLT3 inhibitor, for newly-diagnosed and relapsed/refractory acute myeloid leukemia (AML) with FLT3-ITD mutations; and pexidartinib, an oral CSF1R inhibitor, for tenosynovial giant cell tumor (TGCT). For more information, please visit: www.DSCancerEnterprise.com.
About Daiichi Sankyo
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical products to address diversified, unmet medical needs of patients in both mature and emerging markets. With over 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for hypertension and thrombotic disorders, under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo research and development is primarily focused on bringing forth novel therapies in oncology, including immuno-oncology, with additional focus on new horizon areas, such as pain management, neurodegenerative diseases, heart and kidney diseases, and other rare diseases. For more information, please visit: www.daiichisankyo.com. Daiichi Sankyo, Inc., headquartered in Basking Ridge, New Jersey, is a member of the Daiichi Sankyo Group. For more information on Daiichi Sankyo, Inc., please visit: www.dsi.com.
Daiichi Sankyo, Inc.
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May 2018 Job Code: ONP/18/0008(1)