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1 products found

pp-146

Concentrate for solution for infusion

Dossier type
CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Comments
Indication: 1L advanced cutaneous melanoma (PRAME+/HLA-A*02:01+) Clinical stage: Phase 3 Modality: Biologic (ImmTAC bispecific: soluble TCR against PRAME peptide/HLA-A*02:01 fused to anti-CD3 scFv) Mechanism / Target: Redirects polyclonal T cells to kill PRAME-presenting tumour cells; targets intracellular antigen presented on MHC-I — inaccessible to conventional mAbs Route / form: Intravenous infusion (weekly) Differentiation: Access to intracellular proteome (99%+ of tumour antigens); allele-specific targeting; ImmTAC proven class (tebentafusp approved for uveal melanoma 2022); 1L setting
Manufacturer #39177

Commercial-stage biopharmaceutical with approved ImmTAC bispecific for uveal melanoma. Pioneers TCR-based bispecific T-cell engagers targeting intracellular tumour antigens. Wholly owned Phase 3 cutaneous melanoma programme expanding the ImmTAC platform.
 

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