Anadys Updates On ANA598 Phase II Study In Hepatitis C Patients
Anadys has also announced that all patients have commenced dosing in the second dose cohort, 400mg bid. With patient enrollment in this cohort completed, the company has accelerated
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.