FDA wants cleft birth defect analysis for Vivus weight-loss drug
This article was originally published in Scrip
Investors chose to see the glass as half empty 21 January after Vivus revealed that the US FDA wants an analysis of birth defects associated with one of the two active ingredients in the company's experimental weight-loss drug Qnexa (phentermine/topiramate).
You may also be interested in...
With new funding in hand, Moderna and its infectious disease venture Valera are going full-speed ahead with a Zika vaccine, taking an mRNA approach, which they said could be a more rapid strategy to try to stop the disease.
Allergan CEO Brent Saunders vows not to engage in price gouging and says his firm will limit cost increases to single-digit percentages, occurring only once per year. But it's unclear whether Saunders will stand as a lone wolf in the industry or if others will make similar pledges.
Hillary Clinton's plan to rein in high prices of older medicines, which includes creating a federal panel that has authority to impose fines, may grab headlines, but some analysts think it's unlikely to get very far in a divided Washington.