
Myrio at AACR 2025
April 15, 2025
U.S. Food & Drug Administration (FDA) Approves Investigational New Drug (IND) Application for Myrio’s Lead Product (PHOX2B PC-CAR T) for the Treatment of Neuroblastoma
June 17, 20256th June, 2025
Key Highlights
- Myrio Tx and the University of Pennsylvania’s (UPenn) enduring partnership drives innovation in KRAS based cell therapy for solid tumours
- Myrio Tx’s precision scFv antibodies provided the foundation for UPenn’s NeoCARs. Yielding promising animal model results: Now live in Cancer Cell: https://doi.org/10.1016/j.ccell.2025.05.006
- Remarkably, all mice in the treatment arm achieved complete response (CR) and 100% survival throughout the 60-day study. No toxicity or tumour progression was observed, unlike the control groups
Myrio Tx and University of Pennsylvania’s long standing collaboration has yielded compelling results in developing first-in-class and best-in-class next-generation cancer therapies for solid tumours recently published in Cancer Cell: https://doi.org/10.1016/j.ccell.2025.05.006
Approximately 20% of all solid tumours possess a mutation in the KRAS gene (mKRAS), and as such mKRAS presents a unique and attractive signature for cancer targeting.
Myrio Tx has developed a series of scFv antibodies that precisely target mKRAS. These binders easily discriminate between wildtype and mKRAS, boasting high affinity binding (Kd values from 3-22 nM) resulting in potency and specificity in cancer cell killing in vitro.
These potent and specific scFvs were integrated into the next-generation CAR-T platform – NeoCARs from University of Pennsylvania. Novel enhancements were also leveraged- TCR Knock-Out, to prevent graft-versus-host disease and cellular toxicity; and inducible IL-12-IFN-g cytokines, to boost tumour-killing activity . The safety and potency of this mKRAS anti-cancer therapy was demonstrated in human-tumour mice models, with all animals in this treatment group showing complete response and survival for the duration of the 60-day experiment, exhibiting zero tumor progression or toxicity – in stark contrast to all the other control groups.
These results powerfully demonstrate the precision, effectiveness and potency of Myrio Tx’s antibody engineering platform and their application in translational immune-oncology, making the next-generation of precision immuno-oncology therapeutics closer to patients.