Merck’s new drug application for an investigational intravenous (IV) formulation of NOXAFIL® (posaconazole) receives FDA priority review
18 November 2013 | By Merck
Marketing authorization application also filed with the European Medicines Agency...
List view / Grid view
18 November 2013 | By Merck
Marketing authorization application also filed with the European Medicines Agency...
18 November 2013 | By GlaxoSmithKline
RELVAR® ELLIPTA® is now licensed across 31 European countries...
18 November 2013 | By AMSBIO
Presented by Dr Elad Katz, a senior scientist at AMSBIO, a new on-demand webinar explores the potential of 3D cell-based models for regenerative medicine and drug discovery.
18 November 2013 | By Abbott
Abbott was recognized by The Deal as the best all-around dealmaker in healthcare...
18 November 2013 | By Novo Nordisk
NovoEight® has passed the review by the Committee on Drugs of Japan's Pharmaceutical Affairs and Sanitation Council...
18 November 2013 | By Merck
“I am excited by the results seen for MK-3475 to date as a single agent..."
18 November 2013 | By Amgen
Differences in survival rates were pronounced in the subset of patients with stage IIIB, IIIC or IV M1a disease...
15 November 2013 | By Boehringer Ingelheim
"Run for Diabetes" raises €15,000 towards supporting "Life for a Child Programme..."
14 November 2013 | By Novartis
85% of subjects immunologically protected after receiving second dose of investigational cell culture vaccine when combined with proven MF59® adjuvant...
14 November 2013 | By Bristol-Myers Squibb
“There is a need for the development of short- and long-term diabetes care models and self-management programs..."
14 November 2013 | By Amgen
First long-term data of a PCSK9 Inhibitor to be featured in clinical science: special reports session...
13 November 2013 | By Boehringer Ingelheim
"Our extensive studies have demonstrated that tiotropium Respimat® has the potential to be an effective new treatment..."
13 November 2013 | By Biogen Idec
Phase 3 study showed potential for once- or twice-weekly prophylactic dosing regimens...
13 November 2013 | By Johnson & Johnson
Janssen Biotech, Inc. [“Janssen”] today announced the U.S. Food and Drug Administration (FDA) has approved IMBRUVICA™ (ibrutinib) capsules for the treatment of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy.1 This indication is based on overall response rate (ORR). An improvement in survival or…
13 November 2013 | By Abbott
The Abbott Fund provide $450,000 in grants and healthcare products to help people affected by super typhoon...