Alcon withdraws European Retaane application
The company chose to withdraw the application for Retaane 30mg/ml (anecortave acetate suspension for depot injection) after being informed by the EMEA that it would have to provide
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.