EMA Recommends Sanofi Pasteur A(H1N1) Vaccine Humenza
The CHMP has recommended the marketing authorisation of Humenza vaccine in EU countries for the active immunisation of persons 6 months of age and older against influenza disease
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.
Horizant is an investigational treatment for moderate-to-severe primary Restless Legs Syndrome developed by Xenoport and licensed to GlaxoSmithKline. Depomed noted that unlike Horizant, its proprietary extended release formulations
Lapatinib, in combination with an aromatase inhibitor (AI), is indicated for the treatment of post-menopausal women with hormone receptor (HR)-positive, HER2 (ErbB2) over-expressing metastatic breast cancer. The patients