SBIR/STTR Research Award

Engineered TCR-T Cell Therapy Targeting Driver Mutations in NSCLC

Award identifier dbb522e7e33216ea271a59d8975e356e2bf014d5bdc23e02967aadf9354bbc57Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$400,000

Program and phase

SBIR · Phase I

Award year

2021

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
GIGAMUNE, INC.
Proposal award date
2021-05-01
Contract end date
2022-04-30
UEI
KD8GTLK3VV93
Solicitation number
PA20-260
Topic code
102

Research abstract

PROJECT SUMMARY Project Title: Engineered TCR-T Cell Therapy Targeting Driver Mutations in NSCLC Organization: GigaMune Inc. PI: Matthew J Spindler, Ph.D. Adoptive cell therapies (ACTs) including CAR-T, TCR-T, and TIL therapies have shown strong clinical responses for the treatment of cancer patients for hematological cancers and solid tumors. However, only anti- CD19 CAR-T cell therapies have been FDA approved and commercialized for the treatment of hematological cancers. Numerous TCR-T cell clinical trials are ongoing for the treatment of solid tumors, but these trials target only a handful of well-known cancer-testis and over expressed tumor antigens. Thus, there is a need to develop TCR-T cell therapies that target novel tumor antigens. Recurrent cancer driver mutations and fusion events in genes like KRAS, EGFR, and ALK drive tumorigenesis in numerous cancers including non-small cell lung cancer (NSCLC). Importantly, these mutations are homogenously present within the tumor and the generated neoantigens have shown immunogenicity in cancer patients and healthy individuals across common HLA types. This suggests that TCR-T cell therapies targeting driver mutations would be a safe and effective treatment for NSCLC. The Specific Aim of this Phase I SBIR project is to develop a catalog of natural human TCRs that target recurrent cancer driver gene mutations present in NSCLC patients for use in TCR-engineered autologous or allogeneic ACTs (TCR-T cells). GigaMuneandapos;s unique technology uses microfluidics, genomics, and mammalian display to generate millions-diverse, natively paired TCRab repertoire libraries. The TCRab libraries are immortal, enabling repeated experimentation with a panel of antigens. This will expedite discovery of rare anti- driver mutation TCRs. The project is led by Dr. Matthew J. Spindler, an expert in immunogenomics and inventor of the GigaMune technology and supported by leading NSCLC oncologists Justin Gainor and Alice Shaw (Mass General). After completing this Phase I SBIR project, GigaMune will further develop promising TCRs as TCR-T cell therapies, through in vivo efficacy studies, in vitro safety studies, and manufacturing development.PROJECT NARRATIVE Project Title: Engineered TCR-T Cell Therapy Targeting Driver Mutations in NSCLC Organization: GigaMune Inc. PI: Matthew J Spindler, Ph.D. Cancer remains an intractable disease, but doctors have been achieving incredible results with new therapies that rely on genetic engineering of T cells. We are using microfluidics and DNA sequencing to capture disease- modulating T cells from patients. Antitumor genes from these T cells are then engineered into healthy T cells to create a TCR-engineered T cell therapy.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

8 SBIR/STTR records share this UEI (2018–2025). Reported award amounts total $2,750,294. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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