Europe's CHMP recommends approval of Boehringer Ingelheim's Twynsta and Teva's generic Plavix; updates on rotavirus vaccines

26 July 2010

The European Medicines Agency (EMEA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the granting of a marketing authorization for Twynsta (telmisartan/amlodipine), from independent German drug major Boehringer Ingelheim. The drug is intended for the treatment of essential hypertension. The review for Twynsta began on 23 September 2009 with an active review time of 210 days.

Positive opinion for generics

The Committee also adopted positive opinions recommending the granting of marketing authorizations for the following generic medicines:

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