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Qnexa to be re-filed at FDA for Obesity

Read time: 1 mins
Last updated:19th Sep 2011
Published:19th Sep 2011
Source: Pharmawand
Vivus will resubmit its application to the FDA for Qnexa (phentermine plus topiramate), by the end of October,which is about two months before top-line results are expected from the firm's retrospective observational study assessing fetal outcomes in the offspring of women exposed to topiramate(forming part of Qnexa) during the first trimester of pregnancy. Results of the study are expected by the third quarter of 2012.

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