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Floatz Rating
BB65/100
Confidence
Indicative
v0.2
Sponsor
Queen Mary University of London
Modality
monoclonal_antibody
Development Phase
Phase 4 / Approved
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
65High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
A Study to Learn More About The Safety of Diroximel Fumarate (VUMERITY®) in Participants Who Took it During Pregnancy And About the Health of Their Babies
Active Not Recruiting
Randomized Autologous heMatopoietic Stem Cell Transplantation Versus Alemtuzumab, Cladribine or Ocrelizumab for RRMS (RAM-MS)
Active Not Recruiting
A Study to Evaluate Efficacy, Safety, and Tolerability of Alemtuzumab in Pediatric Patients With RRMS With Disease Activity on Prior DMT
Terminated
Signatures of Immune Reprogramming in Anti-CD52 Therapy of MS: Markers for Risk Stratification and Treatment Response
Unknown
Study of Alemtuzumab in Treatment Refractory MS Subjects/Alemtuzumab Naive & Alemtuzumab Experienced Subjects
Unknown
Keratinocyte Growth Factor to Prevent Autoimmunity After Alemtuzumab Treatment of Multiple Sclerosis
Terminated
Hematopoietic Stem Cell Therapy for Patients With Multiple Sclerosis
Terminated
Examining the Risk of Skin Cancer in Multiple Sclerosis Patients Using Fingolimod: a Population-Based Study
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 · Multiple Sclerosis

AssetSponsorPhaseRating
Alemtuzumab (this asset)Queen Mary University of LondonApprovedBB · 65
CladribineUniversity Hospital, Strasbourg, FranceP4BBB
NabiximolsJazz PharmaceuticalsP4BBB
TeriflunomideSanofiP4BBB
OcrelizumabPolpharma Biologics International AGP4BBB
FampridineMGH Institute of Health ProfessionsP4BBB
NatalizumabBiogenP4BB
FingolimodBiogenP4BB
Interferon ?1 (Human Fibroblast Protein Moiety)BayerP4BB

+42 more in the Multiple Sclerosis 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 Multiple Sclerosis. 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-multiple-sclerosis

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