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Myriad drug to enter brain cancer trial

This new human clinical study will evaluate the potential of MPC-6827 to treat metastatic brain cancer by achieving therapeutic concentrations in the brain that are sufficient to treat

UK regulator could withdraw Alzheimer’s drugs

The National Institute of Clinical Excellence (NICE) has recommended that four cholinesterase inhibitors currently licensed in the UK for use in Alzheimer’s disease, donepezil (Pfizer and Eisai’s Aricept),

Takeda and 3M enter development and marketing pact

Under the terms of this agreement, 3M and Takeda will share further costs of development and, upon successful clinical development and regulatory approvals, the companies will jointly commercialize

NicOx compound beats aspirin in diabetes trial

Increased platelet activation is a feature of diabetes that contributes to the high incidence of cardiovascular events in diabetic patients. NCX 4016 is a novel antithrombotic and vascular

MediciNova anti-anxiety agent enters phase II

MN-305 is described as a serotonin type 1A receptor agonist, and based on preclinical and earlier clinical studies, could hold the potential for rapid onset of anti-anxiety effect

Sunesis presents promising anticancer data

Sunesis’ Aurora kinase inhibitors target cells in the mitotic phase of the cell cycle. In vivo results demonstrate robust activity, including significant tumor growth retardation, exceeding 80% in

Elusys files to begin human anthrax studies

Anthim is a therapeutic monoclonal antibody being developed by Elusys to prevent and treat anthrax infections. Following clearance of the investigational new drug (IND) by the FDA, Elusys

GW speeds up plans to enter US market

In its preliminary results statement of January 19 2005, GW announced that it would embark on a regulatory program in the US for its lead product, Sativex. The