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AZ-004 is being developed for the treatment of agitation in patients with schizophrenia or bipolar disorder. In the CRL, the FDA has stated that their primary clinical safety

Vickers will be responsible for leading global R&D for Shire HGT and for establishing the strategic direction of the company’s pipeline. Vickers will report to Sylvie Gregoire, president

In the letter, the FDA discussed a number of topics, including the need for additional clinical studies, the appropriate patient population, methods for ensuring safe use, and the

de Garidel started his career in 1983 with the Eli Lilly pharmaceutical Group where he held various roles, mainly finance related, firstly in France, then in the US

As per the terms of the agreement, Lundbeck is expected to pay an undisclosed fee as well as product supply payments in exchange for exclusive commercial rights to

Daiichi Sankyo, the holder of the investigational new drug application for ARQ 197 and ArQule’s partner for the development of the compound, will conduct the Phase 3 trial,

The active ingredient in NeuroSTAT, cyclosporin-A, has been used for immunosuppression such as in organ transplantation, NeuroVive said. NeuroVive Pharma CEO Mikael Bronnegard said that the orphan drug

The pre-clinical research was presented at the 8th International M Judah Folkman Conference in Cambridge, Massachusetts, highlighting significant advances in the systemic delivery of RNAi therapeutics. In the

In the study, BSI-201demonstrated that treatment with the drug in combination with gemcitabine/carboplatin results in a improvement in overall survival and a high rate of clinical response in