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Disease
Leukemia, Myeloid
Late-stage therapeutic developmentEmerging research
2
Publications
18
Clinical trials
2016
Latest publication
Latest activity
betaRecent clinical, regulatory, research and industry developments relating to this disease.
Research2016-04-11Blood
Research1966-02-01Annals of internal medicine
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Executive briefingUpdating summary…Momentum: Low
Key developments
- 3 clinical trials expected to report results, the earliest in Q1 2027.
Upcoming Milestones
- Q1 2027Multicenter, Open-label, Randomized, Phase 2 Study of Venetoclax and Azacitidine Plus Cusatuzumab Versus Venetoclax and Azacitidine Alone in Newly Diagnosed AML Patients Who Are Not Candidates for Intensive Therapy
- Q4 2027A Phase 2 Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome
- Q2 2029A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Study of Bleximenib, Venetoclax and Azacitidine for the Treatment of Participants With Newly Diagnosed Acute Myeloid Leukemia Harboring KMT2A Rearrangements or NPM1 Mutations Who Are Ineligible for Intensive Chemotherapy
Major developments
Upcoming trial readoutHigh impact
Results expected Q2 20292026-07-06
Upcoming trial readoutHigh impact
Results expected Q4 20272026-07-07
Clinical MilestonesViewHide
Results expected
- 2026-07-07A Phase 2 Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic SyndromeResults expected Q4 2027
- 2026-07-06A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Study of Bleximenib, Venetoclax and Azacitidine for the Treatment of Participants With Newly Diagnosed Acute Myeloid Leukemia Harboring KMT2A Rearrangements or NPM1 Mutations Who Are Ineligible for Intensive ChemotherapyResults expected Q2 2029
- 2026-05-11Multicenter, Open-label, Randomized, Phase 2 Study of Venetoclax and Azacitidine Plus Cusatuzumab Versus Venetoclax and Azacitidine Alone in Newly Diagnosed AML Patients Who Are Not Candidates for Intensive TherapyResults expected Q1 2027
Recently completed
Other updates
Activity timeline5
- 2026-07-07ClinicalA Phase 2 Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic SyndromeResults expected Q4 2027
- 2026-07-06ClinicalA Phase 3 Randomized, Double-Blind, Placebo-Controlled, Study of Bleximenib, Venetoclax and Azacitidine for the Treatment of Participants With Newly Diagnosed Acute Myeloid Leukemia Harboring KMT2A Rearrangements or NPM1 Mutations Who Are Ineligible for Intensive ChemotherapyResults expected Q2 2029
- 2026-05-11ClinicalMulticenter, Open-label, Randomized, Phase 2 Study of Venetoclax and Azacitidine Plus Cusatuzumab Versus Venetoclax and Azacitidine Alone in Newly Diagnosed AML Patients Who Are Not Candidates for Intensive TherapyResults expected Q1 2027
- 2026-01-31ClinicalA Multi-center, Prospective, Single-arm Study of Venetoclax Combining Chidamide and Azacitidine (VCA) in the Treatment of Refractory/Relapsed Acute Myelogenous Leukemia (R/R AML)Primary completion
- 2026-01-07ClinicalPhase 3 Randomized Trial of DFP-10917 vs Non-Intensive Reinduction (LoDAC, Azacitidine, Decitabine, Venetoclax Combination Regimens) or Intensive Reinduction (High & Intermediate Dose Cytarabine Regimens) for Acute Myelogenous Leukemia Patients in Second, Third, or Fourth SalvageTerminated
Clinical trials
The current development programme across all trial phases.
Clinical programme
18
6
14
6
Late-stage studies
Recruiting
Recently completed
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Publications over time
19662016
Most influential
Major themes3
- Leukocyte Count1
- Leukopenia1
- Lymphocytes1
Leading journals2
- Annals of internal medicine1
- Blood1
Leading researchers8
- Arber DA1
- Bloomfield CD1
- Bodey GP1
- Borowitz MJ1
- Buckley M1
- Cazzola M1
- Freireich EJ1
- Hasserjian R1
Affiliations (unnormalised)6
- Comprehensive Cancer Center1
- Institute of Pathology1
- John Hopkins Medical Institutions1
- Massachusetts General Hospital1
- Stanford University1
- University of Chicago1
Reference
Authoritative identity, definition & identifiers.
Defined in MeSH
Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites.
Identifiers
References & data sources
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.