Baxter expects to complete acquisition of Alpha Therapeutics alpha-1 antitrypsin product and all Alpha plasma collection operations, including 42 U.S. facilities and one central lab, in first half of 2003. The proteinase inhibitor is under review at FDA for treatment of hereditary emphysema. Baxter estimates 200,000 patient population in the U.S. and Europe, half of whom are symptomatic...
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Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.
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A new pilot aims to take Brazil closer to ‘digital transformation.’
Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.
The UK’s research-based pharma industry and medical research charities have set out clear action points to drive greater diversity and inclusion in clinical trials.
Blenrep, GSK’s multiple myeloma therapy, faced a major setback when it was withdrawn from the market in 2022. The drug has since made a return as a second-line therapy, and is on track to being reimbursed in England.
