Floatz logo

Etoposide

Chronic Myelomonocytic Leukemia

Explore 94 assets in Chronic Myelomonocytic Leukemia
Floatz Rating
B62/100
Confidence
Indicative
v0.2
Sponsor
Mayo Clinic
Modality
Small molecule
Development Phase
Phase 3
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
57High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Umbilical Cord Blood Transplant With Added Sugar and Chemotherapy and Radiation Therapy in Treating Patients With Leukemia or Lymphoma
Completed
Personalized NK Cell Therapy in CBT
Recruiting
Clofarabine and Melphalan Before Donor Stem Cell Transplant in Treating Patients With Myelodysplasia, Acute Leukemia in Remission, or Chronic Myelomonocytic Leukemia
Active Not Recruiting
Pomalidomide After Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome
Completed
Clofarabine Followed By Lenalidomide for High-Risk Myelodysplastic Syndromes and Acute Myeloid Leukemia
Completed
PK Study of Oral and IV Clofarabine in High Risk Myelodysplasia+Acute Leukemias
Completed
Clofarabine, Cytarabine, and Filgrastim in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia, Advanced Myelodysplastic Syndrome, and/or Advanced Myeloproliferative Neoplasm
Completed
Phase I Dose-Escalation Trial of Clofarabine Followed by Escalating Doses of Fractionated Cyclophosphamide in Children With Relapsed or Refractory Acute Leukemias
Terminated
Vorinostat, Cytarabine, and Etoposide in Treating Patients With Relapsed and/or Refractory Acute Leukemia or Myelodysplastic Syndromes or Myeloproliferative Disorders
Completed
Combination Chemotherapy With or Without Bone Marrow Transplantation in Treating Children With Acute Myelogenous Leukemia or Myelodysplastic Syndrome
Completed

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
73High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Chronic Myelomonocytic Leukemia

AssetSponsorPhaseRating
Etoposide (this asset)Mayo ClinicP3B · 62
PevonedistatTakedaP3BB
VenetoclaxServier Bio-Innovation LLCP2/3BB
Astx727Taiho Oncology, Inc.P3BB
IdarubicinFred Hutchinson Cancer CenterP3BB
Cyclosporin AFred Hutchinson Cancer CenterP2BB
AzacitidineThe University of Hong KongP3BB
MelphalanCity of Hope Medical CenterP2BB
TacrolimusCity of Hope Medical CenterP2BB

+42 more in the Chronic Myelomonocytic Leukemia cohort

Other indications for Etoposide

IndicationSponsorPhaseRating
Acute Megakaryoblastic LeukemiaP3BBB · 79
Acute Monocytic LeukemiaP3BBB · 79
Acute Myeloblastic Leukemia With MaturationP3BBB · 79

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. Etoposide in Chronic Myelomonocytic Leukemia. 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/etoposide-chronic-myelomonocytic-leukemia

Need depth?

Order a full diligence report on this asset.

Order report →

Are you the sponsor?

Submit your data room for a Verified Rating. The public-data rating remains visible alongside.

Contact →