FDA grants breakthrough therapy status for ACADIA’s Nuplazid
If approved, Nuplazid will establish a new and distinctly different pharmacological approach to treat psychosis. The company has already completed a pivotal Phase III trial of Nuplazid in
South Korea-based Alteogen has signed an exclusive licensing deal worth up to $365m with a global pharmaceutical company, granting worldwide rights to develop and commercialise a subcutaneous biologic product using its Hybrozyme technology.
APD811 is an investigational drug candidate internally discovered and developed by Arena for the treatment of vasospastic diseases, such as PAH. Arena Operations Global Regulatory Affairs senior vice-president
Motolimod is indicated for ovarian cancer patients whose disease has progressed on or recurred after platinum-based chemotherapy. The new Toll-like receptor 8 (TLR8) immunotherapy, motolimid is currently being
The active substance in Somatuline is lanreotide acetate, a somatostatin analogue that inhibits the secretion of several endocrine, exocrine and paracrine amines and peptides. Decision from the FDA