Vascarta Inc, a clinical stage biopharmaceutical company developing therapies for pain, inflammation, and in collaboration with the City University of New York (CUNY), announced on Monday the publication of a preclinical study demonstrating that STO-1, a first-in-class drug candidate, can selectively withdraw glioblastoma (GBM) cells in mice while avoiding harmful autoimmune reactions.
STO-1 is a proprietary hybrid molecule in which curcumin is linked to paclitaxel with a linker that gets broken when STO-1 enters a cell. Vascarta says that during the study, mice treated with STO-1 experienced a 67% long-term survival rate, with several animals achieving complete tumour clearance.
Dr. Probal Banerjee, the senior author and Professor of Biochemistry, Biology, Neuroscience, Chemistry at the College of Staten Island, CUNY, said: "Unlike other immune therapies, which can trigger dangerous autoimmune reactions, STO-1 targets only the tumour-associated cells. This study demonstrates a promising new approach to treating glioblastoma safely."
TIRmed Pharma partners with Bachem to advance production of atopic dermatitis therapy
Fondazione Telethon reports positive opinion for Waskyra marketing authorisation in Europe
Vascarta and CUNY report positive preclinical results in glioblastoma treatment
Cellipont Bioservices and Ernexa Therapeutics form cell therapy partnership
Hemogenyx Pharmaceuticals advances HG-CT-1 trial and opens paediatric recruitment
CStone announces Phase I CS2009 data at ESMO 2025
Merck KGaA to acquire JSR Life Sciences chromatography business to expand Protein A capabilities
Bristol Myers Squibb to acquire Orbital Therapeutics for USD1.5bn to expand cell therapy portfolio
Celltrion launches AVTOZMA IV in the United States following FDA approval
OSE Immunotherapeutics forms strategic alliance with Inserm Transfert and Nantes University
Shoulder Innovations expands I-Series portfolio with launch of InSet 70 Humeral Stem
EMA recommends marketing approval of Alvotech's Gobivaz biosimilar to Simponi