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CHMP says yes to developing world vaccine, Novartis' Seebri Breezhaler, Takeda's Revestive

This article was originally published in Scrip

Executive Summary

The European Medicines Agency's scientific committee, the CHMP, has given the green light for the European Commission to OK a number of new medicines, including Takeda's orphan drug Revestive (teduglutide) for patients with short bowel syndrome. And, for the first time ever, it recommended a vaccine – Sanofi Pasteur's Hexaxim – for use in markets outside the EU.



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