Drug intelligence / Profile preview

ras peptide-specific activated autologous t lymphocytes

Development stage
Phase 1
Lead developer
National Cancer Institute
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

ras peptide-specific activated autologous t lymphocytes is an experimental adoptive cell therapy consisting of a patient's own T lymphocytes that have been sensitized and expanded ex vivo to target mutated Ras proteins. The process involves harvesting T cells from a patient, culturing them with synthetic peptides representing common oncogenic Ras mutations (such as KRAS G12D or G12V), and re-infusing the activated cells back into the patient. These sensitized T cells are designed to recognize and eliminate tumor cells that present these specific mutant Ras neoantigens via the major histocompatibility complex (MHC). Developed primarily by researchers at the National Cancer Institute (NCI), this therapy aims to exploit the high prevalence of Ras mutations in solid tumors, particularly in pancreatic, colorectal, and lung cancers, providing a personalized approach to targeting a key driver of malignancy.

Other names
ras peptide-sensitized autologous T lymphocytesmutant ras-specific activated autologous T-lymphocytesras peptide-specific T cellsmutated ras peptide-specific activated autologous T lymphocytes
02

Targets

Divarasib-KRAS G12C-pMHC (Divarasib-modified KRAS G12C peptide–MHC class I complex)

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