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Alemtuzumab

Sickle Cell Disease

Explore 133 assets in Sickle Cell Disease
Floatz Rating
B60/100
Confidence
Indicative
v0.2
Sponsor
St. Jude Children's Research Hospital
Modality
monoclonal_antibody
Development Phase
Phase 3
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
59High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Haploidentical Donor Hematopoietic Cell Transplant for Sickle Cell Disease
Not Yet Recruiting
Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors
Recruiting
Allo HSCT for High Risk Hemoglobinopathies
Recruiting
Sickle Cell Disease Transplant Using a Nonmyeloablative Approach for Patients With Anti-donor Red Cell Antibody
Recruiting
Non-myeloablative Haploidentical HCT Study for Patients With Sickle Cell Disease, Including Compromised Organ Function
Active Not Recruiting
Do Alemtuzumab Levels Predict T Cell Chimerism After MSD SCT for SCD?
Unknown
TMLI and Alemtuzumab for Treatment of Sickle Cell Disease
Active Not Recruiting
Addition of JSP191 (C-kit Antibody) to Nonmyeloablative Hematopoietic Cell Transplantation for Sickle Cell Disease and Beta-Thalassemia
Active Not Recruiting
Reduced Intensity Transplantation for Severe Sickle Cell Disease
Suspended
T-Cell Depleted Alternative Donor Bone Marrow Transplant for Sickle Cell Disease (SCD) and Other Anemias
Recruiting
Show 19 more trials
Minimizing Toxicity in HLA-identical Sibling Donor Transplantation for Children With Sickle Cell Disease
Recruiting
Stem Cell Transplant in Patients With Severe Sickle Cell Disease
Terminated
Haploidentical Transplantation With Pre-Transplant Immunosuppressive Therapy for Patients With Sickle Cell Disease
Recruiting
Nonmyeloablative Stem Cell Transplant in Children With Sickle Cell Disease and a Major ABO-Incompatible Matched Sibling Donor
Recruiting
Nonmyeloablative Haploidentical Peripheral Blood Mobilized Hematopoietic Precursor Cell Transplantation for Sickle Cell Disease
Active Not Recruiting
Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders
Recruiting
Bone Marrow Transplantation vs Standard of Care in Patients With Severe Sickle Cell Disease (BMT CTN 1503)
Completed
Abatacept for GVHD Prophylaxis After Hematopoietic Stem Cell Transplantation for Pediatric Sickle Cell Disease
Completed
Nonmyeloablative Conditioning for Mismatched Hematopoietic Stem Cell Transplantation for Severe Sickle Cell Disease
Terminated
Nonmyeloablative Peripheral Blood Mobilized Hematopoietic Precursor Cell Transplantation for Sickle Cell Disease and Beta-thalassemia in People With Higher Risk of Transplant Failure
Active Not Recruiting
SCD-Haplo: Phase II Study of HLA-Haploidentical SCT for Aggressive SCD
Terminated
Ph I/II Study of Allogeneic SCT for Clinically Aggressive Sickle Cell Disease (SCD)
Active Not Recruiting
CD34+Selection for Partially Matched Family or Matched Unrelated Adult Donor Transplant
Completed
Haploidentical PBMC Transplant for Severe Congenital Anemias
Active Not Recruiting
HSCT For Patients With High Risk Hemoglobinopathies Using Reduced Intensity
Completed
Evaluating the Safety and Effectiveness of Bone Marrow Transplants in Children With Sickle Cell Disease (BMT CTN 0601)
Completed
Haploidentical Stem Cell Transplant for Patients With Sickle Cell Disease and Prior Stroke or Abnormal Transcranial Ultrasound
Completed
Improving the Results of Bone Marrow Transplantation for Patients With Severe Congenital Anemias
Unknown
Induction of Stable Chimerism for Sickle Cell Anemia
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 · Sickle Cell Disease

AssetSponsorPhaseRating
Alemtuzumab (this asset)St. Jude Children's Research HospitalP3B · 60
GlutamineAin Shams UniversityP4BBB
HydroxyureaSt. Jude Children's Research HospitalP4BB
Magnesium MetallicumMedical College of WisconsinP3BB
NivestimSt. Jude Children's Research HospitalP4BB
CrizanlizumabNovartis PharmaceuticalsP4BB
FentanylUniversity College DublinP4BB
NepentheOman Medical Speciality BoardP4BB
ARGTanta UniversityP3BB

+42 more in the Sickle Cell Disease 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 Sickle Cell Disease. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 11, 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-sickle-cell-disease

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