Tumor Neoantigen Vaccine Schematic

What Is a Neoantigen Cancer Vaccine ?

Neoantigens are tumor-specific protein fragments arising from cancer-cell mutations and are absent from normal tissue. Genomic sequencing and AI-based algorithms can be used to identify patient-specific neoantigens and design personalized vaccine therapies.

Video Player is loading.
Current Time 0:00
Duration 0:30
Loaded: 40.33%
Stream Type LIVE
Remaining Time 0:30
 
1x
    • Chapters
    • descriptions off, selected
    • captions off, selected

      GT601: An AI-Driven, Next-Generation Neoantigen Cancer Vaccine

      GT601 is built on GRIT Bio's proprietary AI-assisted neoantigen discovery platform, leveraging the Company's extensive internal functional validation data and multi-omics data accumulated through TIL R&D. The neoantigen sequences selected can better achieve specific immune responses and reprogram the tumor microenvironment, thereby reducing exhausted CD8+ T cells and regulatory T cells (Tregs). GT601 holds promise for breakthroughs in the post-surgical adjuvant setting and may synergize with multiple therapeutic modalities including TIL, in vivo CAR-T, and CAR-iNKT cell therapies.

      FIH Clinical

      GT601

      GT601 is a personalized neoantigen tumor vaccine leveraging proprietary TIL R&D data for AI model training to drive vaccine development.

      Indications

      Solid tumors

      Technology Platform

      NEOvigator® / APC‑Targeted LNP DeliveryTechnology

      AI-driven Algorithms Represent All Steps of Antigen Presentation And T Cell Response

      AI-Driven Algorithm Covering the Full Process of Antigen Processing, Presentation, Recognition, and T Cell Response

      NeoAntigen Discovery and Functional Validation Platform

      The platform is designed to fully recapitulate the entire process of antigen processing, presentation and recognition, as well as the resulting T-cell response, including:

      • Isolation and expansion of autologous antigen-presenting cells to evaluate neoantigen expression, processing, MHC binding and presentation;

      • Patient-derived tumor-infiltrating lymphocytes and peripheral blood mononuclear cell (PBMC)-derived T cells to evaluate T-cell recognition of presented antigens and the resulting T-cell responses.

      Traditional MHC-binding prediction

      CD8+ Only Focused

      Prediction Success Rate: <10%

      GRIT NEOvigator® Neoantigen Discovery Platform

      Covers Both CD4+ & CD8+

      Prediction Success Rate: ~70%

      APC-Targeted LNP Delivery System

      APC-targeted lipid nanoparticles are designed to combine efficient mRNA delivery with precise targeting, reduced liver uptake and scalable manufacturing.

      Lipoplex (LPX) Schematic

      Lipoplex (LPX)

      Classic LNP Schematic

      Classic LNP

      CategoryAttributeLipoplex (LPX)Classic LNP (2nd Gen)APC-Targeted LNP
      PhysicochemicalFunctional LipidPermanently Cationic LipidIonizable LipidIonizable Lipid
      Particle Size200~400 nm60~120 nm60~120 nm
      EfficacyAPC-Targeting SpecificityYesNoYes
      mRNA Delivery EfficiencyLowHighHigh
      SafetyBiodegradabilityPoorHighHigh
      Relative ToxicityHighLowLow
      Liver LeakageLowVery HighLow
      CMCManufacturing ScalabilityDifficultEstablishedEstablished
      Colloidal StabilityLowHighHigh
      Polydispersity IndexHigh (>0.2)Low (<0.2)Low (<0.2)

      Learn More About Tumor Neoantigen Therapy

      We welcome medical institutions and research organizations to explore clinical collaboration and technical exchange on tumor neoantigen vaccines.