Opportunity
Federal Register #2026-14981
NCI Seeks Partners for NPM1 Mutation-Specific T Cell Receptors for AML Therapy
Posted
July 24, 2026
Identifier
2026-14981
NAICS
541715, 541711, 325412, 541380, 541690
The National Cancer Institute (NCI), part of the National Institutes of Health under the Department of Health and Human Services, is seeking partners for a government-owned invention targeting Acute Myeloid Leukemia (AML): - Government Buyer: - Department of Health and Human Services - National Institutes of Health - National Cancer Institute - Technology Offered: - NPM1 Mutation-Specific T Cell Receptors (TCR6 and TCR7) - Designed for targeted adoptive T cell therapy in AML patients expressing the NPM1 mutation and HLAA*11:01 - Recognizes the neoepitope AVEEVSLRK derived from mutant NPM1 - Product Details: - Part number: E20020250 - Pre-clinical validation stage - Demonstrated robust, specific cytotoxicity against AML cell lines and patient-derived samples - No cross-reactivity to normal cells or unrelated HLA alleles, indicating a strong safety profile - Opportunity Type: - Seeking research co-development partners or licensees - No commercial OEMs or vendors are named; this is a government-owned invention - Unique Requirements: - Focus on AML patients with HLAA*11:01 and NPM1 mutation - Technology is intended for adoptive T cell therapy applications - Emphasis on specificity and safety in targeting cancer cells
Description
The National Cancer Institute (NCI) is seeking research co-development partners or licensees for NPM1 Mutation-Specific T Cell Receptors aimed at targeted treatment of Acute Myeloid Leukemia (AML). This invention involves two highly specific T cell receptors, TCR6 and TCR7, which recognize a neoepitope derived from mutant NPM1 presented in the context of HLAA*11:01. Pre-clinical results show robust and specific cytotoxicity against leukemia cell lines and patient-derived AML samples expressing the NPM1 mutation and HLAA*11:01, with no cross-reactivity to normal cells or unrelated HLA alleles. The technology represents a potential adoptive T cell therapy for AML with a significant unmet medical need and enhanced safety profile.