DOAN'S PILLS BACK PAIN RELIEF COMPARATIVE AD CLAIMS CHALLENGED BY FTC in a complaint against Ciba Self-Medication issued June 26. The Federal Trade Commission is seeking to impose an order requiring Ciba to "cease and desist" from representing, without "competent and reliable supporting evidence," that Doan's pills are "more effective than other over-the-counter analgesic drugs for relieving back pain or any other kind of pain."
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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.’
While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.
Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.
Highlights from Day Four of the BIO International Convention include policy concerns helping constrain dealmaking, Novartis discussing its approach to partnering, and Generate looking for funding to move into Phase III.
