CDKN2A is a known negative prognostic marker in glioblastoma that frequently undergoes homozygous deletion (between 40% to 60% of the patients). RXcel's smart RNA molecules turn this gene into a therapeutic target which offers a rational for a transformative approach to treatment, laying the foundation for a more precise clinical intervention.
Despite current standard-of-care treatments (surgery, radiotherapy, and temozolomide), median survival for patients with glioblastoma remains just 12 to 15 months. There have been few advances over the past two decades, and recurrence is almost inevitable. Novel, targeted therapies are urgently needed.
Compared to other solid tumors, glioblastoma sees disproportionately low clinical trial activity — despite its severity and poor prognosis. This highlights a major gap in innovation and investment that RXcel is aiming to address.
An idea is born, Simon and Michal lay the foundation in Basel, Switzerland.
06/08/2023In collaboration with FHNW (University of Applied Sciences Northwestern Switzerland) , RXcel has successfully conducted a proof-of-concept experiment, funded by Innosuisse. This study demonstrated a statistically significant difference of effector protein production in specific cell lines with and without CDKN2A, using fluorescent reporter constructs (eGFP). The underlying concept has been discussed with scientists in the relevant fields, who have expressed confidence in its potential.
01/03/2024Dr. Marion Salvador joins as a Scientific Consultant. Private funding has enabled us to revalidate and optimize in vitro results in close collaboration with FHNW.
05/01/2025RXcel signs a Memorandum of Understanding with the Czech Academy of Sciences. This also marks the beginning of our collaboration with Prof. Petr Svoboda and his group.
08/01/2025Prof. Ghazaleh Tabatabai joins as another Strategic Consultant and brings long-standing experience from clinical practice and research in the field of neuro-oncology.
11/27/2025In close collaboration with our academic partners, we are currently optimizing our target RNA, aiming to reach in vivo readiness by Q1 2027. This includes the integration of new RNA designs to build a versatile therapeutic platform, along with ongoing validation of the molecular mechanism and assessment of potential off-target effects. To advance into in vivo studies, additional funding will be required, and RXcel has initiated early-stage discussions to secure the necessary resources.
12/31/2025Founder
Biologist with experience in lipid nano carriers and RNA therapeutics
Founder
Physicist and passionate data scientist, extensive experience in cancer biology
Strategic Consultant
Molecular biologist specialized on post-transcriptional regulations and RNA processing, professor at Charles University and a group leader at Institute of Molecular Genetics
Strategic Consultant
A neurologist, a physician scientist and a professor of Neurology and Neuro-oncology at the University of Tübingen,
Scientific Consultant
Cancer biologist and translational cancer researcher with passion for innovation