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DAIICHI SANKYO

USupdated 5mo ago
community read0 votes
pipeline
0
marketed
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phase 3
0
catalysts ytd
0
approvals ytd
0
recalls ytd
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Pipeline(0)

no pipeline products on record

📅 Upcoming

no upcoming catalysts on record

🕒 Recent(90d)

nothing in the last 90 days
view all catalysts →

Active trials

  • phase2A Study of Patritumab Deruxtecan (HER3-DXd) in Combination With Trastuzumab Deruxtecan (T-DXd) in Participants With HR-Positive, HER2-Low or HER2-Ultralow Unresectable or Metastatic Breast Cancerrecruitingn=220
  • phase3A Study of Bempedoic Acid/Ezetimibe/High-intensity Statin in Patients Without Cardiovascular Eventsnot yet recruitingn=103
  • phase3Study of Dato-DXd Plus Pembrolizumab vs Pembrolizumab Alone in the First-line Treatment of Subjects With Advanced or Metastatic NSCLC Without Actionable Genomic Alterationsactive not recruitingn=740
  • phase1A Study of Valemetostat Tosylate in Combination With DXd ADCs in Subjects With Solid Tumorsactive not recruitingn=210
  • phase3HERTHENA-Lung02: A Study of Patritumab Deruxtecan Versus Platinum-based Chemotherapy in Metastatic or Locally Advanced EGFRm NSCLC After Failure of EGFR TKI Therapyactive not recruitingn=586
  • phase1First-in-Human Trial of DS1025a in Participants With Advanced Solid Tumorsrecruitingn=45
  • phase2A First-in-Human Trial of DS3790a in Participants With Hematological Malignanciesrecruitingn=420
  • phase3Study of Datopotamab Deruxtecan Plus Carboplatin or Cisplatin Versus Gemcitabine Plus Carboplatin or Cisplatin in Participants With Locally Advanced or Metastatic Urothelial Carcinomarecruitingn=630
🐶 Hiring Signal
No open roles indexed yet — view DAIICHI SANKYO jobs →

News

  • Summit partners with AstraZeneca and Daiichi; Eccogene earns $50M milestone
    Plus news about Regeneron. Summit Therapeutics to test cancer drug with Datroway: The biotech agreed to partner with AstraZeneca and Daiichi Sankyo on a clinical trial collaboration, testing its Tr…
    endpoints · 1d ago
  • Merck inks up to $2.13B deal to dine with SciBrunch, gain rights to preclinical KRAS inhibitor
    Merck continues to diversify its cancer efforts as the clock ticks down on Keytruda’s patent, picking up rights to a preclinical oncology asset in a deal that could exceed $2 billion.
    biospace · 5d ago
  • STAT+: Pharmalittle: We’re reading about GLP-1s becoming lifestyle drugs, a setback for Merck and Daiichi, and more
    Once promoted as tools to address obesity as a medical issue, GLP-1 drugs are increasingly being marketed as a way to look and feel better
    stat · 5d ago
  • Merck, Daiichi end plans to seek speedy approval of lung cancer ADC
    The FDA indicated that the data generated so far wouldn’t support an accelerated clearance of “I-DXd,” a setback that erases an edge Merck and Daiichi had over multiple fast-moving competitors.
    biopharma_dive · 5d ago
  • Merck, Daiichi Sankyo retract accelerated approval request for lung cancer ADC
    Merck and Daiichi Sankyo’s withdrawal of an accelerated approval request for the antibody-drug conjugate ifinatamab deruxtecan is a “net positive” for rivals like GSK and Roche, according to RBC Ca…
    biospace · 6d ago
  • Merck, Daiichi scrap FDA application for B7-H3 ADC in lung cancer
    In yet another setback to the Merck and Daiichi Sankyo partnership, the companies said they have pulled their FDA accelerated approval application for an antibody-drug conjugate (ADC) in certain sm…
    endpoints · 6d ago
  • Merck, Daiichi pull lung cancer filing after FDA pushback deals another blow to $4B deal
    Daiichi Sankyo and Merck & Co. have withdrawn an antibody-drug conjugate (ADC) filing after the FDA said they lacked the data for accelerated approval in a lung cancer population.
    fiercebiotech · 6d ago
  • Roche, MediLink notch phase 3 lung cancer win but trail GSK on cross-trial survival
    MediLink has reported phase 3 results on a Roche-partnered antibody-drug conjugate. The small-cell lung cancer trial hit its primary endpoint, although the B7-H3-directed ADC’s median overall survi…
    fiercebiotech · 20d ago
  • BioNTech sets survival standard in hard-to-treat cancer ahead of pivotal readout
    BioNTech has linked gotistobart to a median overall survival of 18.5 months in relapsed lung cancer patients, adding to evidence that the anti-CTLA-4 antibody is better than the standard of care.
    fiercebiotech · 23d ago
  • GSK’s Hansoh-partnered ADC lays down marker for lung cancer scrap with Merck
    GSK’s risvutatug rezetecan has achieved a median overall survival of 18.5 months in a phase 3 trial, painting the antibody-drug conjugate as a threat to Amgen and Merck & Co. in the lung cancer field.
    fiercebiotech · 23d ago
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