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Cpx-351

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Explore 75 assets in Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
Floatz Rating
BB67/100
Confidence
Indicative
v0.2
Sponsor
National Cancer Institute (NCI)
Modality
UNKNOWN
Development Phase
Phase 2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
58High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Testing the Use of Combination Therapy in Patients With Persistent Low Level Acute Myeloid Leukemia Following Initial Treatment, The ERASE Study (A MyeloMATCH Treatment Trial)
Not Yet Recruiting
Testing the Effects of Novel Therapeutics for Newly Diagnosed, Untreated Patients With High-Risk Acute Myeloid Leukemia (A MyeloMATCH Treatment Trial)
Recruiting
MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)
Recruiting
Comparing the Addition of an Anti-Cancer Drug, Pomalidomide, to the Usual Chemotherapy Treatment (Daunorubicin and Cytarabine Liposome) in Newly Diagnosed Acute Myeloid Leukemia With Myelodysplastic Syndrome-Related Changes
Active Not Recruiting
CPX-351 for the Treatment of Secondary Acute Myeloid Leukemia in Patients Younger Than 60 Years Old
Active Not Recruiting
Liposomal Cytarabine, Daunorubicin, and Gemtuzumab Ozogamicin for the Treatment of Relapsed Refractory Pediatric Patients With Acute Myeloid Leukemia
Completed
CPX-351 and Glasdegib for Newly Diagnosed Acute Myelogenous Leukemia With MDS Related Changes or Therapy-related Acute Myeloid Leukemia
Active Not Recruiting
Testing the Effect of Taking Ruxolitinib and CPX-351 in Combination for the Treatment of Advanced Phase Myeloproliferative Neoplasms
Terminated
A Post-Marketing Observational Study of VYXEOS™
Completed
Geriatric Assessment & Genetic Profiling to Personalize Therapy in Older Adults With Acute Myeloid Leukemia
Completed
Show 3 more trials
Liposome-encapsulated Daunorubicin-Cytarabine, Fludarabine Phosphate, Cytarabine, and Filgrastim in Treating Younger Patients With Relapsed or Refractory Acute Myeloid Leukemia
Completed
CPX-351 in Treating Patients With Newly Diagnosed, High-Risk Acute Myeloid Leukemia
Completed
EAP of CPX-351 (VYXEOS) for Patients 60-75 Years of Age With Secondary AML
Approved For Marketing

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
81High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

AssetSponsorPhaseRating
Cpx-351 (this asset)National Cancer Institute (NCI)P2BB · 67
DaunomycinNational Cancer Institute (NCI)P3BBB
CytarabineNational Cancer Institute (NCI)P3BBB
NivestimCity of Hope Medical CenterP2/3BBB
IdarubicinFred Hutchinson Cancer CenterP2/3BB
EtoposideM.D. Anderson Cancer CenterP3BB
CyclophosphamideFred Hutchinson Cancer CenterP3BB
MelphalanCity of Hope Medical CenterP2BB
MitoxantroneInstitut de Recherches Internationales ServierP2BB

+42 more in the Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome cohort

Other indications for Cpx-351

IndicationSponsorPhaseRating
Myelodysplastic SyndromeP2/3B · 63
Acute Myeloid LeukemiaP4B · 61
Myeloproliferative NeoplasmP2B · 60

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. Cpx-351 in Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome. 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/cpx-351-therapy-related-acute-myeloid-leukemia-and-myelodysplastic-syndrome

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