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Gilteritinib

Myelodysplastic/Myeloproliferative Neoplasm

Explore 42 assets in Myelodysplastic/Myeloproliferative Neoplasm
Floatz Rating
CCC48/100
Confidence
Indicative
v0.2
Sponsor
M.D. Anderson Cancer Center
Modality
Small molecule
Development Phase
Phase 1/2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
33Indicative
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Azacitidine, Venetoclax, and Gilteritinib in Treating Patients With Recurrent/Refractory FLT3-Mutated Acute Myeloid Leukemia, Chronic Myelomonocytic Leukemia, or High-Risk Myelodysplastic Syndrome/Myeloproliferative Neoplasm
Recruiting

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
95High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Myelodysplastic/Myeloproliferative Neoplasm

AssetSponsorPhaseRating
Gilteritinib (this asset)M.D. Anderson Cancer CenterP1/2CCC · 48
EtoposideM.D. Anderson Cancer CenterP3BBB
MelphalanM.D. Anderson Cancer CenterP2/3BBB
BusulfanumJacqueline Garcia, MDP2/3BBB
Cyclosporin AMemorial Sloan Kettering Cancer CenterP3BBB
CytarabineFred Hutchinson Cancer CenterP3BBB
Anti-Human T-Lymphocyte Immunoglobulin, RabbitM.D. Anderson Cancer CenterP2/3BBB
FludarabineFred Hutchinson Cancer CenterP3BBB
TacrolimusM.D. Anderson Cancer CenterP2BBB

+42 more in the Myelodysplastic/Myeloproliferative Neoplasm cohort

Other indications for Gilteritinib

Scientific Foundation

Strength of the underlying biology: target validation, tractability, modality fit, and how related mechanisms have fared.
NR

Planned for methodology v0.2.

Development Feasibility

How realistically the program can be executed, drawing on modality precedent, enrollment dynamics, and sponsor delivery.
NR

Planned for methodology v0.2.

Commercial Opportunity

Commercial prize: addressable population, unmet need, and the value case for the indication.
NR

Planned for methodology v0.2.

IP & Exclusivity

Exclusivity position, covering patent protection and freedom-to-operate runway.
NR

Planned for methodology v0.2.

Manufacturing & Supply

Manufacturing and supply readiness, driven by modality process and scale-up risk.
NR

Planned for methodology v0.2.

Related assets

Citation

Floatz Terminal. Gilteritinib in Myelodysplastic/Myeloproliferative Neoplasm. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 8, 2026.
Accessed July 14, 2026.
https://terminal.floatz.ai/assets/gilteritinib-myelodysplasticmyeloproliferative-neoplasm

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