China Aoxing Completes Tilidine Phase III Trial
The company said that the drug is designated as a Class III New Medicine with approximately at least four-year market exclusivity protection, upon marketing clearance by the China
The US Food and Drug Administration (FDA) is set to review Kowa Pharmaceuticals America’s new drug application (NDA) for K-911, an investigational once-daily eye drop aimed at reducing intraocular pressure (IOP) in open-angle glaucoma (OAG) or ocular hypertension (OHT) patients.