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US regulators approve GSK’s allergy nasal spray

Veramyst is the first prescription nasal steroid spray to demonstrate consistent and significant improvement in relieving overall allergic eye symptoms, which included red, itchy and watery eyes, in

Wyeth stockholders reject CEO, chairman separation

In addition, stockholders voted to defeat stockholder proposals regarding: disclosing the company’s animal welfare policy; preparing a report on limiting the supply of prescription drugs in Canada, and

FDA rejects Merck’s Arcoxia

Merck is seeking market authorization for Arcoxia to treat osteoarthritis in the US, where it has been under review since December 2003. The drug is in the same

Alexion gets recommendation for Soliris

Based upon the positive recommendation, marketing authorization by the European Commission is expected in two to three months. Soliris, a designated orphan medicinal product, is intended to reduce

Meda buys product portfolio from Wyeth

The acquired portfolio include CNS drug Seresta, an anti-anxiety agent used for sleep disorders and substance-withdrawal symptoms. No employees will transfer from Wyeth to Meda in conjunction with

FDA requests additional drug data from Cipher

The FDA indicated that Cipher’s application is approvable subject to the resolution of two remaining issues. In addition to one question related to chemistry, manufacturing and controls, the

J&J schizophrenia drug receives positive opinion

The company said it anticipates receiving the marketing authorisation from the European Commission by mid-year 2007. The paliperidone prolonged release tablets marketing authorisation application is based on an