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COMPANY RESEARCH

GRIT Biotechnology

GRIT disclosed T-cell-targeted mRNA/LNP GT801 and a separate lentiviral direction. GT801 is also developed through spinout Vivacta Bio; the two company profiles describe a shared program lineage, not two independent drugs. GRIT’s TIL clinical stages are separate.

Company at a glance

Corporate information

Company entity
GRIT Biotechnology
Headquarters / principal office
Beijing relocation in 2025; public contact address remains in Shanghai ↗
Founded
2019 ↗
Ownership / capital status
PrivateSeries B+ (2024 historical disclosure) ↗
Official corporate reference
https://www.grit-bio.com/vivo-cart ↗
Latest financing / award identified
2024 · Series B+ · Undisclosed ↗
LinkedIn company page
Independent company page not verified

Company history gives the year and round, without an exact amount.

Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

GRIT disclosed T-cell-targeted mRNA/LNP GT801 and a separate lentiviral direction. GT801 is also developed through spinout Vivacta Bio; the two company profiles describe a shared program lineage, not two independent drugs. GRIT’s TIL clinical stages are separate.

Program / serviceTarget / indicationRepresentative stageEvidence & scope
GT801CD19 · See program source; distinguish indicationsExploratory human study / IITHuman research disclosed or registered; efficacy is not established.

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

No cataloged update explicitly mentions this company.

Same-field reading (not company-specific)
Nature

ANGPTL3 base-editing study reports sustained protein lowering in nonhuman primates

A Nature study delivered guide RNA and base-editor mRNA in GalNAc lipid nanoparticles to inactivate liver ANGPTL3. Nonhuman primates showed mean ANGPTL3 protein reductions exceeding 90%, with durability assessed through three years after one dose. Lipid reductions were observed in animal models. Human liver-cell testing assessed selected off-target sites; the paper does not report human clinical efficacy.

Nature Materials

In situ CAR engineering and nanoparticle-mediated TREM2 degradation for macrophage reprogramming in malignant ascites

A Nature Materials study describes mRNA-loaded LNPs that reprogram tumor-associated macrophages into Claudin18.2-targeting CAR macrophages. The lipid formulation also promotes TREM2 internalization and degradation, reshaping immune responses. The original abstract reports tumor suppression and longer survival with PD-1 blockade in mice, plus ex vivo patient-sample findings. These findings do not demonstrate clinical efficacy in treated patients.

CSPC Pharmaceutical Group

CSPC initiates first Chinese center for SYS6055-003 in vivo CAR-T trial

CSPC announced initiation of the first Chinese center for SYS6055-003, a Phase 1/2 trial in relapsed or refractory B-cell non-Hodgkin lymphoma. SYS6055 uses lentiviral vectors to generate CD19-targeting CAR-T cells in vivo. The company said recruitment and screening are underway following October clinical-trial authorization. Center initiation does not establish patient dosing, efficacy, or marketing approval.

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Sources & open questions

  • Unverified financing, founding dates, and clinical status are not inferred. Acquisitions/options are not financing rounds.
  1. GRIT Biotechnology — primary program / ownership disclosure ↗GRIT Biotechnology · Undated unless stated in source; checked 2026-11-04
  2. GRIT Biotechnology — supporting primary disclosure ↗GRIT Biotechnology · Undated unless stated in source; checked 2026-11-04
  3. GRIT Bio — Company History ↗GRIT Biotechnology ·

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