Alnuctamab

drug
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Summary

Alnuctamab (CHEMBL6068570) is a phase-3 clinical-stage antibody; indicated across 1 condition including plasma cell myeloma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 1 condition
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL6068570
NameAlnuctamab
TypeAntibody
Max phase3

Also known as: Alnuctamab, ALNUCTAMAB

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

1 indication (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
plasma cell myeloma3MONDO:0009693EFO:0001378

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE13
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06232707PHASE3WITHDRAWNA Study to Evaluate Efficacy and Safety of Alnuctamab Compared to Standard of Care Regimens in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)
NCT06121843PHASE1RECRUITINGA Study to Evaluate the Safety, Effectiveness and Tolerable Dose of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma
NCT07219563PHASE1RECRUITINGAlnuctamab for Refractory SLE (LATTE Study)
NCT06163898PHASE1TERMINATEDA Study to Evaluate Alnuctamab in Combination With Mezigdomide in Participants With Relapsed and/or Refractory Multiple Myeloma

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).