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This designation provides Antigenics with, among other benefits, ten years of potential market exclusivity if the product is approved for marketing in the European Union (EU). The FDA

Under the agreement, Valentis has agreed to grant Schering a worldwide license to its GeneSwitch gene regulation and PINC polymer delivery technologies for research purposes on a non-exclusive

The lawsuit had been filed in a US federal district court on February 8, 2005, alleging false advertising and unfair competition claims relating to the Nicodrops product. The

InterveXion has received a $3 million grant to conduct clinical trials for the first antibody treatment for addiction to the drug phencyclidine, or PCP. The business development grant

The FDA approval was based on results of a large randomized, double-blind, placebo-controlled study involving 277 patients with pulmonary arterial hypertension (PAH). The study measured the exercise capability

The study, which compared the five-day dosing (320mg once-daily) to the FDA-approved seven-day dosing, achieved its primary endpoint (non-inferior clinical response rate at the follow-up visit), illustrating the

The study was designed to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of escalating doses of ALTU-238 in normal healthy volunteers. Altus now plans to initiate a multi-center

Blue Cross is using the ZixVPM (Virtual Private Messenger) to enforce its email security policies in order to ensure secure handling of confidential information to its users, including

If the drug continues in development and ultimately is approved and marketed, Ligand could receive additional milestone payments and double-digit royalties on product sales. Thrombocytopenia (decreased platelet count)