Drug intelligence / Profile preview

neldaleucel

Development stage
Phase 1
Lead developer
Marker Therapeutics
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, TCR-Engineered T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Tumor-Infiltrating Lymphocytes (TILs) → Native Immune Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous
01

Overview

Neldaleucel (MT-601) is an autologous, non-genetically modified, multi-tumor-associated antigen (multiTAA)-specific T cell therapy developed by Marker Therapeutics for the treatment of pancreatic adenocarcinoma. Utilizing the proprietary MAR-T (Multi-Antigen Recognizing T cell) platform, the therapy consists of cytotoxic T lymphocyte lines that simultaneously target six tumor-associated antigens highly expressed in pancreatic cancer: PRAME, NY-ESO-1, Survivin, MAGE-A4, SSX2, and WT1. Unlike CAR-T or TCR-T therapies, neldaleucel does not require genetic engineering, which may reduce manufacturing complexity and improve safety by avoiding insertional mutagenesis. The therapy is currently being evaluated in the Phase 1 PANACEA study in combination with front-line chemotherapy for patients with newly diagnosed locally advanced unresectable or metastatic pancreatic adenocarcinoma.

Brand names
MultiTAA
Other names
MT-601MT601MT 601
02

Targets

WT1 (Wilms tumor protein)SSX2 (Synovial sarcoma X breakpoint protein 2)PRAME (Preferentially expressed antigen in melanoma)NY-ESO-1 (New york esophageal squamous cell carcinoma 1)pHLA (Human leukocyte antigen class I and class II peptide-presenting complexes)BIRC5 (Survivin)MAGEA4 (Melanoma-associated antigen A4)

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