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Floatz Rating
B62/100
Confidence
Indicative
v0.2
Sponsor
Acerta Pharma BV
Modality
monoclonal_antibody
Development Phase
Phase 1/2
Status
Dormant
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
51High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
ACP-196 (Acalabrutinib) in Combination With Pembrolizumab, for Treatment of Hematologic Malignancies
Completed
Brentuximab Vedotin + Rituximab as Frontline Therapy for Pts w/ CD30+ and/or EBV+ Lymphomas
Terminated
Alvocidib, Fludarabine Phosphate, and Rituximab in Treating Patients With Lymphoproliferative Disorders or Mantle Cell Lymphoma
Completed

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
95High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Hairy Cell Leukemia

AssetSponsorPhaseRating
Rituximab (this asset)Acerta Pharma BVP1/2B · 62
CyclophosphamideKite, A Gilead CompanyP2BB
CediranibAlexey Danilov, MDP1/2B
FludarabineKite, A Gilead CompanyP2B
LenalidomideJoseph TuscanoP1/2B
ObinutuzumabJoseph TuscanoP1/2B
Cyclosporin AFred Hutchinson Cancer CenterP2B
AlemtuzumabFred Hutchinson Cancer CenterP2B
EtoposideCity of Hope Medical CenterP1/2B

+33 more in the Hairy Cell Leukemia cohort

Other indications for Rituximab

IndicationSponsorPhaseRating
Lymphoblastic LymphomaP4BBB · 75
Grade III Lymphomatoid GranulomatosisP2BBB · 74
Testicular LymphomaP2BBB · 74

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. Rituximab in Hairy Cell 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/immunoglobulin-g-1-human-mouse-monoclonal-idec-c2b8-gamma1-chain-anti-human-antigen-cd-20-disulfide-with-human-mouse-monoclonal-idec-c2b8-kappa-chain-dimer-hairy-cell-leukemia

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