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Acute Myeloid Leukemia

Oncology 13 original drugs
13
Novel Drugs
6
Reformulations
0
Active Trials
18
Drug Targets

Phase 3 Readouts Pro

10 active Phase 3 trials with confidence-graded completion dates.

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Q2 2027
mocravimod
Priothera SAS
Estimated · fresh NCT05429632
Q3 2027
XY0206
Shijiazhuang Yiling Pharmaceutical Co. Ltd
Estimated · stale NCT05876832
Q3 2027
Venetoclax
AbbVie
Estimated · fresh NCT03844048
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Treatments by Mechanism

Top 12 mechanisms across 47 industry trials with a known mechanism of action.

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Menin Inhibitor
4 trials 4 active 1 sponsor
BCL-2 Inhibitor
13 trials 3 active 1 sponsor
Nucleoside Metabolic Inhibitor
11 trials 2 active 7 sponsors
Kinase Inhibitor
7 trials 1 active 2 sponsors
IDH1
1 trials 1 active 1 sponsor
Telomerase/hTR
1 trials 1 active 1 sponsor
DNA
3 trials 3 sponsors
Alkylating Drug
2 trials 2 sponsors
Programmed Death Receptor-1 Blocking Antibody
2 trials 1 sponsor
Nuclear Export Inhibitor
1 trials 1 sponsor
CD30-directed Immunoconjugate
1 trials 1 sponsor
DNA polymerase alpha/DNA primase/Ribonucleotide reductase
1 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Clinical Pipeline by Phase

503 industry-sponsored trials across 263 sponsors

Precision Medicine Biomarkers

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Biomarkers used for patient selection in Acute Myeloid Leukemia

Reformulations (6 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Related Indications

Other Oncology indications

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology