Positive nine year data for Accentia lymphoma vaccine
As well as the 95% survival rate at the median 9.2 year follow-up, 45% of patients that received the vaccine remained in continuous first clinical remission at their
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.