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Daiichi Sankyo Company (4568) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Bevacizumab, R-DxdFallopian Tube Cancer, Ovarian Cancer, Peritoneal Cancer, Ovarian NeoplasmsPhase IIIRecruitingA Study of Raludotatug Deruxtecan With or Without Bevacizumab as First-Line Maintenance Treatment in Non-HRD-Positive Advanced Ovarian Cancer (MK-5909-006, (ENGOT-ov102/GOG-3141/ REJOICE-Ovarian 04)Aug 17, 2026
Bevacizumab, Ds-6000A, R-Dxd, Mvasi, AvastinFallopian Tube Cancer, Primary Peritoneal Cancer, High-Grade Serous Ovarian Cancer, Endometrioid Epithelial OvarianPhase IIINot Yet RecruitingA Study of Raludotatug Deruxtecan (R-DXd) With or Without Bevacizumab as Maintenance Therapy in Second-Line Platinum-Sensitive Recurrent Ovarian Cancer (REJOICE-Ovarian03)Aug 03, 2026
Carboplatin, Bevacizumab, Gemcitabine, Paclitaxel, Pegylated Liposomal Doxorubicin, R-Dxd, Raludotatug Deruxtecan, Ds-6000A, Mvasi, AvastinOvarian Cancer, Fallopian Tube Cancer, Peritoneal CancerPhase IIINot Yet RecruitingA Clinical Trial of Raludotatug Deruxtecan (R-DXd) With or Without Bevacizumab in Participants With Ovarian Cancer Who Have Progressed During Treatment With PARP-inhibitors Treatment on First Line Maintenance (MK-5909-008/ENGOT-ov107/GOG-3142 / REJOICE-Ovarian05)Jul 29, 2026
Carboplatin, Pembrolizumab, Pemetrexed, Ds-1103A, Ds-3939ASolid Tumor, Metastatic Non-Small Cell Lung Cancer, Locally Advanced Non-Small Cell Lung Cancerphase1AndPhase2Not Yet RecruitingA Study of DS-3939a in Participants With Solid TumorsJul 28, 2026
Her3-Dxd, Trastuzumab Deruxtecan, Patritumab Deruxtecan, T-DxdHormone Receptor Positive, Her2-Low Or Her2-Ultralow, Unresectable Or Metastatic Breast Cancerphase1AndPhase2RecruitingA 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 CancerJul 08, 2026―
Ds1025aAdvanced Solid Tumor, Metastatic Solid Tumor, Unresectable Solid TumorPhase INot Yet RecruitingFirst-in-Human Trial of DS1025a in Participants With Advanced Solid TumorsJun 26, 2026
Trastuzumab Deruxtecan, Trastuzumab, Palbociclib, Endocrine Therapy, Pertuzumab, T-Dxd, Enhertu, Herceptin, IbranceAdvanced Breast Cancer, Metastatic Breast Cancer, Her2 Positive, Hr PositivePhase IIINot Yet RecruitingT-DXd Based Therapy Followed by Endocrine Therapy Plus Dual HER2 Blockade in First-line HER2+/ HR+ Metastatic Breast Cancer and Retreatment With T-DXdJun 25, 2026
Ifinatamab Deruxtecan, I-DxdMalignant Neoplasmphase1AndPhase2RecruitingA Study of Ifinatamab Deruxtecan in Pediatric Participants With Relapsed or Refractory Solid Tumors (MK-9999-01D/LIGHTBEAM-U01)Jun 01, 2026
Rosuvastatin, Atorvastatin, Ezetimibe, Bempedoic AcidHypercholesterolemia, Mixed Dyslipidemia, Coronary AtherosclerosisPhase IIINot Yet RecruitingA Study of Bempedoic Acid/Ezetimibe/High-intensity Statin in Patients Without Cardiovascular EventsMar 11, 2026
Rescue Medication, I-Dxd, Ifinatamab DeruxtecanOesophageal Squamous Cell Carcinomaphase1AndPhase2RecruitingA Clinical Trial of Ifinatamab Deruxtecan in People With Advanced Esophageal Cancer (MK-3475-06F)Feb 05, 2026

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Daiichi Sankyo Company (JP:4568) have in its pipeline
Daiichi Sankyo Company JP:4568 is currently developing the following drugs: Bevacizumab, R-Dxd, Bevacizumab, Ds-6000A, R-Dxd, Mvasi, Avastin, Carboplatin, Bevacizumab, Gemcitabine, Paclitaxel, Pegylated Liposomal Doxorubicin, R-Dxd, Raludotatug Deruxtecan, Ds-6000A, Mvasi, Avastin, Carboplatin, Pembrolizumab, Pemetrexed, Ds-1103A, Ds-3939A, Her3-Dxd, Trastuzumab Deruxtecan, Patritumab Deruxtecan, T-Dxd, Ds1025a, Trastuzumab Deruxtecan, Trastuzumab, Palbociclib, Endocrine Therapy, Pertuzumab, T-Dxd, Enhertu, Herceptin, Ibrance, Ifinatamab Deruxtecan, I-Dxd, Rosuvastatin, Atorvastatin, Ezetimibe, Bempedoic Acid, Rescue Medication, I-Dxd, Ifinatamab Deruxtecan, Datopotamab Deruxtecan, Dexamethasone Mouthwash, Atorvastatin, Ezetimibe, Bempedoic Acid, Cetuximab, Patritumab Deruxtecan, Sacituzumab Tirumotecan, Rescue Medications, Mk-1084, Darolutamide, Valemetostat, Carboplatin, Etoposide, Atezolizumab, Gocatamig, I-Dxd, Rescue Medications, Docetaxel, Datopotamab Deruxtecan, Ds3790a, Combination Drug, Rosuvastatin, Bempedoic Acid, Ezetimibe, Ds9051b, Dato-Dxd, Ds3610a, Pembrolizumab, Ds5361b, Nab-Paclitaxel, Trastuzumab Deruxtecan, Paclitaxel, Capecitabine, Patritumab Deruxtecan, Liposomal Doxorubicin, Docetaxel, Prednisone, Ifinatamab Deruxtecan, Bempedoic Acid 180 Mg Tablet, Pembrolizumab, Pemetrexed, Trastuzumab Deruxtecan, Chemotherapy, Raludotatug Deruxtecan, Docetaxel, Enzalutamide, Abiraterone, Ifinatamab Deruxtecan, Mk-5684, Patritumab Deruxtecan, Pembrolizumab, Bevacizumab, Paclitaxel, Carboplatin, Raludotatug Deruxtecan, Rescue Medication, Quizartinib High Dose, Quizartinib Low Dose, Bevacizumab, Trastuzumab Deruxtecan, Pembrolizumab, Cyclophosphamide, Paclitaxel, Capecitabine, Carboplatin, Olaparib, Patritumab Deruxtecan, Doxorubicin Hydrochloride, Epirubicin Hydrochloride, Ifinatamab Deruxtecan, Raludotatug Deruxtecan, Docetetaxel, Docetaxel, R-Dxd, I-Dxd, Pembrolizumab, Oxaliplatin, Leucovorin, 5-Fluorouracil, Levoleucovorin, I-Dxd, Durvalumab, Ifinatamab Deruxtecan, Gocatamig, Quizartinib, Rufinamide, Quizartinib. These drug candidates are in various stages of clinical development as the company works toward FDA approval.