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Daiichi Sankyo Company –
Oncology Drug Pipeline Insights – June 2021

Oncology New Molecules Development Strategy

Team OmicsX by Team OmicsX
June 14, 2021 - Updated On May 30, 2022
in Big Pharma, Onco Pipeline Insights, Oncology
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Daiichi Sankyo is the second largest pharma company in Japan, developing small molecules & biologics for various diseases and was came into existence in 2005, through the merger of Sankyo Co., Ltd. and Daiichi Pharmaceutical Co., Ltd.

Global Oncology Intelligence Global Oncology Intelligence
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2. Daiichi Sankyo Active Clinical Stage Oncology Pipeline (12 Active Molecules)

  • 1. Daiichi Sankyo Major Oncology Drug Approvals
  • 2. Daiichi Sankyo Active Clinical Stage Oncology Pipeline (12 Active Molecules)
    MoleculeTargetPhaseIndicationNCT NumberMol Type
    Pirtobrutinib /
    LOXO-305
    BTKIIIMantle-Cell LymphomaNCT04662255Small Molecule
    IIIChronic Lymphocytic LeukemiaNCT04666038
    Small Lymphocytic Lymphoma
    LY3484356SERDIMetastatic Breast CancerNCT04188548Small Molecule
    Endometrial Cancer
    LY3475070CD73IAdvanced CancerNCT04148937Small Molecule
    LY3295668Aur A KinaseINeuroblastomaNCT04106219Small Molecule
    LY3410738IDH1IAdvanced Solid TumorsNCT04521686Small Molecule
    Advanced Hematologic MalignanciesNCT04603001

Daiichi Sankyo Active Oncology Pipeline Drug Description

  • Teserpaturev is an oncolytic herpes simplex virus type 1 (HSV-1), which has triple mutations in the viral genome that replicate selectively in cancer cells and enhance the induction of antitumor immune response while maintaining high safety.
  • Teserpaturev is co-developed by Daiichi Sankyo and Dr. Tomoki Todo, Professor at the Institute of Medical Science, University of Tokyo.
  • U3-1402 is a novel HER3-antibody-drug conjugate (ADC) composed of the HER3 antibody patritumab and a novel topoisomerase I inhibitor, for the treatment of Colorectal Cancer.
  • Turalio / Pexidartinib is a small-molecule receptor tyrosine kinase (RTK) inhibitor of proto-oncogene receptor tyrosine kinase (KIT), colony-stimulating factor-1 receptor (CSF1R) and FMS-like tyrosine kinase 3 (FLT3), with antineoplastic activity.
  • DS-1001b is an oral selective inhibitor of mutant IDH1 R132X that was designed to penetrate the blood-brain barrier.
  • DS-1055 is a GARP directed immuno-oncology therapy, in patients with advanced or metastatic solid tumors who have progressed on standard treatments including checkpoint inhibitors. GARP is highly expressed on activated regulatory T cells (Tregs) and contributes to their immunosuppressive activity.
  • DS-6000 is a CDH6 directed antibody drug conjugate (ADC), in patients with advanced renal cell carcinoma or ovarian cancer with disease progression following standard treatment.
  • CDH6 overexpression is associated with tumor growth and proliferation and has been correlated with poor prognosis in renal cell carcinoma.
  • DS-6157 is a potential first-in-class GPR20 targeting ADC and the fifth DXd ADC in the oncology pipeline of Daiichi Sankyo to enter clinical development.
  • DS-7300, a B7-H3 (B7 homologue 3) targeting antibody-drug conjugate (ADC), is designed using Daiichi Sankyo’s proprietary DXd technology, and comprised of a humanized anti-B7-H3 monoclonal antibody, attached to a novel topoisomerase I inhibitor payload by a tetrapeptide-based linker.
  • Designed utilizing Daiichi Sankyo’s proprietary DXd ADC technology, DS-6157 is comprised of a humanized anti-GPR20 monoclonal antibody, which is attached to a novel topoisomerase I inhibitor payload by a tetrapeptide-based linker.
Jump to section

2. Daiichi Sankyo Active Clinical Stage Oncology Pipeline (12 Active Molecules)

  • 1. Daiichi Sankyo Major Oncology Drug Approvals
  • 2. Daiichi Sankyo Active Clinical Stage Oncology Pipeline (12 Active Molecules)
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