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Alemtuzumab

Myelodysplastic Syndrome

Explore 296 assets in Myelodysplastic Syndrome
Floatz Rating
BB66/100
Confidence
Indicative
v0.2
Sponsor
University Hospital Tuebingen
Modality
monoclonal_antibody
Development Phase
Phase 2/3
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
67High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Alpha/Beta TCD HCT in Patients With Inherited BMF Disorders
Recruiting
Azacytidine Prior to in Vivo T-cell Depleted Allo Stem Cell Transplant for Patients With Myeloid Malignancies in CR
Completed
Efficacy Study of T Cell Depleted Allogeneic Non-myeloablative Stem Cell Transplant
Completed
Mismatched Family Member Donor Transplantation for Children and Young Adults With High Risk Hematological Malignancies
Completed
Chemotherapy and Unrelated Donor Stem Cell Transplantation for Patients With Cancers of the Blood and Immune System
Completed
Sirolimus, Tacrolimus, and Antithymocyte Globulin in Preventing Graft-Versus-Host Disease in Patients Undergoing a Donor Stem Cell Transplant For Hematological Cancer
Completed
Clofarabine and Non-Myeloablative Allogeneic Hematopoietic Transplantation
Terminated
Combination Chemotherapy With or Without Gemtuzumab Ozogamicin or Tipifarnib in Treating Patients With Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndromes
Completed
Donor Stem Cell Transplant in Treating Patients With High-Risk Hematologic Cancer
Terminated
Alemtuzumab, Fludarabine Phosphate, and Total-Body Irradiation Followed by Cyclosporine and Mycophenolate Mofetil in Treating Patients Who Are Undergoing Donor Stem Cell Transplant for Hematologic Cancer
Completed
Show 2 more trials
Alemtuzumab and Combination Chemotherapy Followed By Donor Lymphocytes in Treating Patients Who Are Undergoing Donor Stem Cell Transplant for Hematologic Cancer
Completed
Nonmyeloablative Allogeneic Stem Cell Transplantation From HLA-Matched Unrelated Donor for the Treatment of Hematologic Disorders
Completed

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
65High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Myelodysplastic Syndrome

AssetSponsorPhaseRating
Alemtuzumab (this asset)University Hospital TuebingenP2/3BB · 66
CyclophosphamideSawa Ito, MDP4BB
NivestimCity of Hope Medical CenterP4BB
BusulfanumSawa Ito, MDP4BB
DaunomycinOHSU Knight Cancer InstituteP3BB
CytarabineThe First Affiliated Hospital of Soochow UniversityP4BB
FludarabineCity of Hope Medical CenterP4BB
IdarubicinOHSU Knight Cancer InstituteP4BB
SitagliptinIndiana UniversityP2BB

+42 more in the Myelodysplastic Syndrome cohort

Other indications for Alemtuzumab

IndicationSponsorPhaseRating
Relapsing-Remitting Multiple SclerosisP4BBB · 73
Myelodysplastic/Myeloproliferative NeoplasmP2BB · 71
Chronic Myeloid LeukemiaP2/3BB · 71

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. Alemtuzumab in 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/immunoglobulin-g1-human-rat-monoclonal-campath-1h-gamma1-chain-anti-human-antigen-cd52-disulfide-with-human-rat-monoclonal-campath-1h-light-chain-dimer-myelodysplastic-syndrome

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