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The watchdog filed a complaint in the US District Court for the District of Delaware. It wants the court to prohibit the pharma from submitting repetitive and baseless filings with

Acticor Biotech had already secured €1,4M in the first closing, which brings the total amount invested to €2,9M. This new fund will enable Acticor Biotech to pursue the

GBM is a particularly aggressive brain tumor, with a poor prognosis. GW has received Orphan Drug Designation from the U.S. Food and Drug Administration (FDA) and the European

Perrigo has notified Valeant Pharmaceuticals North America LLC and Dow Pharmaceutical Sciences, Inc. (Valeant) the owner of both the New Drug Application and patents listed in FDA's Orange

The company claims that Parsabiv is the first new therapy approved for the condition in 12 years. It is designed to be administered intravenously three times per week

The company has submitted a marketing authorization application (MAA) to the European Medicines Agency (EMA). Ariad’s US marketing application is currently under the US Food and Drug Administration

The addition of Vault Submissions Publishing unifies publishing capabilities and enterprise content management to streamline end-to-end submission development. Now life sciences companies can plan, review, publish, archive, and

Clinical investigators will assess the safety and efficacy of Immunovaccine's DPX-Survivac cancer vaccine candidate in combination with Merck's checkpoint inhibitor Pembrolizumab in patients with recurrent, platinum-resistant ovarian cancer.

Concurrently, Chondrial announced the licensing of a novel investigational technology, CTI-1601, for the treatment of Friedreich's Ataxia from Indiana University Research and Technology Corp. (IURTC) and Wake Forest