Synonyms: JNJ-64407564 | JNJ64407564 | talquetamab-tgvs | Talvey®
talquetamab is an approved drug (FDA & EMA (2023))
Compound class:
Antibody
Comment: Talquetamab (JNJ-64407564) is a humanized, IgG4 bispecific monoclonal antibody that engages the orphan GPCR GPRC5D that's expressed on majority of malignant plasma cells from multiple myeloma (MM) patients and CD3ε on T cells [3]. It has amino acid substitutions in its Fc region to minimise binding to Fcγ receptors and antibody-directed effector functions. The peptide sequences for talquetamab's heavy and light chains are claimed in Janssen's patent US10562968B2 [1]. In preclinical studies talquetamab promoted immune killing of MM cells, including cells from patients with daratumumab-refractory disease [4].
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No information available. |
Summary of Clinical Use ![]() |
Talquetamab (JNJ-64407564) was progressed to phase 3 evaluations in patients with relapsed/refractory MM. Both the FDA and EMA granted approval in August 2023, for heavily pre-treated relapsed or refractory MM [2]. |
Clinical Trials | |||||
Clinical Trial ID | Title | Type | Source | Comment | References |
NCT04586426 | A Study of the Combination of Talquetamab and Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma | Phase 1 Interventional | Janssen Research & Development, LLC | ||
NCT04634552 | A Study of Talquetamab in Participants With Relapsed or Refractory Multiple Myeloma | Phase 2 Interventional | Janssen Research & Development, LLC | ||
NCT05455320 | A Study Comparing Talquetamab in Combination With Daratumumab or in Combination With Daratumumab and Pomalidomide Versus Daratumumab in Combination With Pomalidomide and Dexamethasone in Participants With Relapsed or Refractory Multiple Myeloma | Phase 3 Interventional | Janssen Research & Development, LLC | ||
NCT05461209 | A Study of Comparing Talquetamab to Belantamab Mafodotin in Participants With Relapsed/Refractory Multiple Myeloma | Phase 3 Interventional | Janssen Research & Development, LLC |
External links ![]() |
For extended ADME data see the following: European Medicines Agency (EMA) |