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Anti-Bcma/Anti-Cd3 T-Cell Engaging Bispecific Antibody Abbv-383

Plasma Cell Myeloma

Explore 475 assets in Plasma Cell Myeloma
Floatz Rating
B63/100
Confidence
Indicative
v0.2
Sponsor
Universitätsklinikum Hamburg-Eppendorf
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.
65Moderate confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Etenta-Isa-VRd in Newly Diagnosed High-Risk Multiple Myeloma
Not Yet Recruiting
A Study to Assess A Change in Disease Activity and Adverse Events of Intravenous Etentamig and Daratumumab (Etentamig+D) Compared to Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Adult Participants With Newly Diagnosed Multiple Myeloma Not Eligible for Transplant
Recruiting
Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereblon E3 Ligase Modulatory Drug (CELMoD) Agent Assessing Adverse Events and Change in Disease Activity in Adult Participants With Relapsed or Refractory Multiple Myeloma
Recruiting
A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult Participants With Multiple Myeloma Receiving Etentamig (ABBV-383) as an Intravenous (IV) Infusion Alone or in Combination With Oral, IV, Subcutaneous Daratumumab; Lenalidomide; Dexamethasone; Carfilzomib
Recruiting
Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutaneous (SC) Injection in Adult Participants With Relapsed or Refractory Multiple Myeloma
Active Not Recruiting
Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Standard Available Therapies in Adult Participants With Relapsed or Refractory Multiple Myeloma
Recruiting
A Study to Assess Adverse Events of Intravenously (IV) Infused Etentamig (ABBV-383) in Adult Participants With Relapsed or Refractory Multiple Myeloma
Recruiting
A Study to Assess Adverse Events and Change in Disease Activity of Intravenously (IV) Infused Etentamig (ABBV-383) in Combination With Anti-Cancer Regimens for the Treatment of Adult Participants With Relapsed/Refractory Multiple Myeloma
Active Not Recruiting
A Study to Assess Adverse Events and Change in Disease State of Intravenously (IV) Infused Etentamig (ABBV-383) of Adult Participants With Relapsed or Refractory Multiple Myeloma in Japan
Active Not Recruiting
A Study of TNB-383B in Participants With Relapsed or Refractory Multiple Myeloma
Active Not Recruiting
Show 1 more trial
Expanded Access for TNB-383B in a Subject With Relapsed/Refractory Multiple Myeloma
No Longer Available

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
59High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Plasma Cell Myeloma

AssetSponsorPhaseRating
Anti-Bcma/Anti-Cd3 T-Cell Engaging Bispecific Antibody Abbv-383 (this asset)Universitätsklinikum Hamburg-EppendorfP3B · 63
Hyaluronidase FihjMassachusetts General HospitalP4BBB
FilanesibPETHEMA FoundationP2BBB
Vincristine SulfateRoswell Park Cancer InstituteP3BBB
Cyclosporin ASeoul National University HospitalP3BBB
Anti-Human T-Lymphocyte Immunoglobulin, RabbitUniversity of BirminghamP4BBB
Epoetin AlfaMayo ClinicP3BB
Arsenic TrioxideDuke UniversityP2BB
SorafenibOHSU Knight Cancer InstituteP2BB

+42 more in the Plasma Cell Myeloma cohort

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. Anti-Bcma/Anti-Cd3 T-Cell Engaging Bispecific Antibody Abbv-383 in Plasma Cell Myeloma. 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/anti-bcmaanti-cd3-t-cell-engaging-bispecific-antibody-abbv-383-plasma-cell-myeloma

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