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Hematology
Blood disease treatments including therapies for hemophilia, sickle cell disease, and myelodysplastic syndromes.
Companies
0
Pipeline Drugs
622
Key People
645
Hematology Pipeline (622 drugs)
Commercial: 90Phase 3: 55Preclinical: 53Approved: 51Pre-clinical: 47Phase 1: 31Phase 2: 30Marketed: 29Phase 1/2: 29Discovery: 20Research: 14Phase III: 11Development: 7Service: 6Not specified: 6Market: 5ANDA Pending: 5IND-Enabling: 4Phase 2/3: 4Tool/Platform Development: 4Phase I/II: 4Under Development: 3Phase 1b: 3Clinical: 3commercial: 3Launched: 2BLA Submitted: 2Phase 2/Phase 3: 2Pre-market: 2Research Use Only: 2Phase not specified: 2Clinical-stage: 2Commercial Expansion: 2Phase 1b/2a: 2Phase I: 2Phase 3 (inferred from ASH presentation): 2Development/Commercial: 2Feasibility: 2Pre-clinical/Research: 2Phase II: 2Approved / Phase 3: 2ANDA Approved: 2Phase 2b: 2Various (Partner-led): 2Clinical Trials: 2Phase 3-ready: 2Not Disclosed: 1Development & Expansion: 1Assay Menu Expansion: 1Integrated Solution: 1Solution: 1Limited Launch: 1R&D / Integration: 1Commercial (Distribution): 1Phase 2a: 1Platform/Service: 1Service/Diagnostic: 1Commercial Service: 1Phase 1/Window-of-Opportunity: 1Commercial & Development: 1Commercial & Expansion: 1Development / Early Commercial: 1Planned: 1Commercial Launch: 1Commercial (ex-US); FDA Breakthrough Designation (US): 1Commercial (ex-US): 1Expanded Access: 1Clinical Trial: 1Development & Validation: 1Service Offering: 1Pre-NDA: 1Approved (CE Mark): 1Phase 3 / Registration: 1Commercial / Line Extension: 1Early Commercial/Clinical: 1Pre-clinical through Post-marketing: 1Pre-clinical / Early Clinical: 1Commercial / Generic Development: 1Phase 1/Preclinical: 1Clinical Stage: 1Pre-clinical / CTA Cleared: 1Device Development: 1Phase 1/2 (not specified): 1Varies by Sponsor Protocol: 1Launch/Commercialization: 1Phase 4: 1Pivotal: 1NDA Filed: 1Pre-clinical/Validation: 1Research/Development: 1Commercial (LDT): 1Proof-of-Concept: 1Registrational: 1development: 1Phase III / Marketed: 1Marketed / Phase 4: 1Marketed / Phase 2/3: 1Filed: 1Phase 1-3: 1Various: 1Research to Phase 3: 1Registration: 1Late-Stage (Phase 3): 1Discovery / Preclinical / Early Clinical: 1Preclinical/Phase I: 1Discovery/Preclinical: 1Preclinical/Discovery: 1Phase 1a/b: 1Phase 1/2 / Pivotal Path: 1
| Drug | Company | Indication | Phase |
|---|---|---|---|
| GS1191 | Gritgen Therapeutics | Hemophilia A | Phase 1 |
| lomonitinib | Lomond Therapeutics | Acute Myeloid Leukemia (AML) | IND-Enabling |
| lonitoclax | Lomond Therapeutics | Chronic Lymphocytic Leukemia (CLL) | Phase 1 |
| Menin Inhibitor | Lomond Therapeutics | Acute Myeloid Leukemia (AML) | Discovery |
| Stem Cell Therapy for Blood Diseases | GIOSTAR | Sickle Cell Anemia, Leukemia, Lymphoma, Thalassemia | Not Disclosed |
| Stem Cell Therapy for Type 1 Diabetes | GIOSTAR | Diabetes (Type 1) | Under Development |
| Stem Cell Therapy for Neurodegenerative Diseases | GIOSTAR | Alzheimer’s, Parkinson’s, ALS, Multiple Sclerosis | Under Development |
| Stem Cell Therapy for Autoimmune Diseases | GIOSTAR | Lupus, Crohn's, Vasculitis, Scleroderma | Under Development |
| PYRUKYND (mitapivat) | Agios Pharmaceuticals | Pyruvate kinase (PK) deficiency — adults | Approved |
| AG-946 | Agios Pharmaceuticals | Hemolytic anemias and other indications | Phase 2 |
| Multiple undisclosed preclinical programs | Agios Pharmaceuticals | Undisclosed rare diseases | Preclinical |
| IDHIFA (enasidenib) — DIVESTED | Agios Pharmaceuticals | Relapsed/refractory AML with IDH2 mutation | Approved |
| TIBSOVO (ivosidenib) — DIVESTED | Agios Pharmaceuticals | Relapsed/refractory AML with IDH1 mutation | Approved |
| MaaT013 | MaaT Pharma | Acute Graft-versus-Host Disease (aGvHD) | Phase 3 |
| MaaT033 | MaaT Pharma | Supportive care in Hemato-Oncology | Phase 2 |
| MaaT03X | MaaT Pharma | Solid Tumors (with ICI) | Research |
| DxC 500 AU Chemistry Analyzer | Beckman Coulter Diagnostics | Core Laboratory Chemistry Testing | Launched |
| DxI 9000 Access Immunoassay Analyzer | Beckman Coulter Diagnostics | High-throughput Immunoassay Testing | Launched |
| Digital Hematology Solutions | Beckman Coulter Diagnostics | Hematology / CBC Analysis | Development & Expansion |
| Neurodegenerative Disease Assays (GFAP, NfL, pTau-217) | Beckman Coulter Diagnostics | Neurology / Alzheimer's Disease Research | Assay Menu Expansion |
| Sepsis Host-Response & AMR Solutions | Beckman Coulter Diagnostics | Sepsis Diagnosis & Management | Integrated Solution |
| Etiometry Clinical Intelligence Platform | Beckman Coulter Diagnostics | Critical Care / High-Acuity Patient Management | Commercial |
| Advantaged Workflows | Beckman Coulter Diagnostics | Laboratory Operational Efficiency | Solution |
| Accrufer (ferric maltol) | Shield Therapeutics | Iron Deficiency Anemia (IDA) in adults | Commercial |
| Feraccru (ferric maltol) | Shield Therapeutics | Iron Deficiency Anemia (IDA) in adults | Commercial |
| Ferric Maltol | Shield Therapeutics | IDA in patients with Inflammatory Bowel Disease (IBD) | Phase 3 |
| Dupixent (dupilumab) | Regeneron | Chronic Obstructive Pulmonary Disease (COPD) | Phase 3 |
| Odronextamab | Regeneron | Relapsed/Refractory Follicular Lymphoma & DLBCL | Phase 3 |
| Pozelimab | Regeneron | Complement 3 Glomerulopathy (C3G) | Phase 3 |
| Garetosmab | Regeneron | Fibrodysplasia Ossificans Progressiva (FOP) | Phase 3 |
| Linvoseltamab | Regeneron | Relapsed/Refractory Multiple Myeloma | Phase 3 |
| Fianlimab + Cemiplimab | Regeneron | Advanced Melanoma (1L adjuvant) | Phase 3 |
| REGN1908-1909 (Fel d 1 mAb) | Regeneron | Cat Allergy | Phase 3 |
| VEGF C-D | Regeneron | Neovascular Age-Related Macular Degeneration (nAMD) | Phase 2/3 |
| Narsoplimab | Omeros | HSCT-TMA | BLA Submitted |
| OMS906 | Omeros | Paroxysmal Nocturnal Hemoglobinuria (PNH) | Phase 2 |
| OMIDRIA | Omeros | Cataract Surgery | Marketed |
| Apitegromab (SRK-015) | Scholar Rock | Spinal Muscular Atrophy (Types 2 & 3) | Phase 3 |
| SRK-181 | Scholar Rock | Solid Tumors (Immuno-Oncology) | Phase 1 |
| SRK-439 | Scholar Rock | Obesity / Muscle Wasting | Preclinical |
| CellaVision Software Updates | CellaVision | Digital Cell Morphology for Peripheral Blood | Commercial |
| Bone Marrow Aspirate Application | CellaVision | Digital Morphology for Bone Marrow Aspirates | Limited Launch |
| AI & Deep Learning Integration | CellaVision | Enhanced Pre-classification & Decision Support | R&D / Integration |
| Reagent Portfolio Expansion | CellaVision | Hematology Staining & Slide Preparation | Commercial |
| INB-400 | IN8bio | Newly Diagnosed Glioblastoma (GBM) | Phase 2 |
| INB-200 | IN8bio | Newly Diagnosed Glioblastoma (GBM) | Phase 1 |
| INB-100 | IN8bio | Leukemia (post-Hematopoietic Stem Cell Transplant) | Phase 1 |
| INB-300 / INB-330 | IN8bio | Acute Myeloid Leukemia (AML) & other cancers | Preclinical |
| INB-500 | IN8bio | Undisclosed Cancers | Preclinical |
| NexCAR19 (talicabtagene autoleucel, Tali‑cel™) | ImmunoACT | CD19‑positive B‑cell acute lymphoblastic leukemia and large B‑cell lymphoma | Commercial |
Key People in Hematology
DY
Dr. Yi Rao
Founder
Gritgen Therapeutics
ID
Iain Dukes
CEO
Lomond Therapeutics
NS
Nikolay Savchuk
COO
Lomond Therapeutics
AB
Amy Burd
CSO
Lomond Therapeutics
BL
Brian Ledwith
Chief Development Officer
Lomond Therapeutics
FP
Fraser Pickersgill
Head CMC
Lomond Therapeutics
JB
John Byrd
Interim Chief Medical Officer
Lomond Therapeutics
DA
Dr. Anand Srivastava
Chairman and Founder
GIOSTAR
DE
Dr. Eleanor Vance
CEO
ClotProtect
DR
Dr. Rajiv Mehta
CSO
ClotProtect
BG
Brian Goff
Chief Executive Officer
Agios Pharmaceuticals
SG
Sarah Gheuens, M.D., Ph.D.
Chief Medical Officer, Head of R&D
Agios Pharmaceuticals
CJ
Cecilia Jones
Chief Financial Officer
Agios Pharmaceuticals
TM
Tsveta Milanova
Chief Commercial Officer
Agios Pharmaceuticals
KV
Krishnan Viswanadhan, Pharm.D.
Chief Strategy and Operations Officer
Agios Pharmaceuticals