OncoZenge AB, a pharmaceutical company developing BupiZenge™, a non-opioid based treatment for oral pain, announced that ongoing stability studies for the revised formulation of BupiZenge™ show positive results.
Stability studies of BupiZenge™ are ongoing in line with previous communication from the company. The data now obtained shows 3 months of positive results within the desired limits of the specification for the development of the latest formulation. This data complements earlier data and analyzes and confirms the flexibility that OncoZenge now possesses to take BupiZenge™ to the next clinical development phase and market approval, with different packaging options.
“We are pleased to confirm that we continue to receive positive stability data for the latest formulation of BupiZenge,” says Stian Kildal, CEO of OncoZenge. “This confirms the competence, methods, and experience that the team now possesses to create stable product formulations with bupivacaine in combination with different packaging options. In addition to our readiness to take BupiZenge™ into a Phase 3 program for Europe, these insights are also valuable for future opportunities to create product variants for other indications and dosage-levels, or for other future pipeline candidates with bupivacaine.”