Astellas, XenoPort Regnite tablet secures Japanese approval
The New Drug Application (NDA) filing for Regnite was backed by the safety and efficacy data from the Phase 2 study in RLS patients. The long-term safety study
China-based Biocytogen Pharmaceuticals has entered a non-exclusive licensing agreement with Qilu Pharmaceutical for a fully human VHH antibody molecule.
The data demonstrated that Dimebon did not achieve statistically significant results for either of the two co-primary endpoints including the Alzheimer’s Disease Assessment Scale and the Alzheimer’s Disease