FDA wants more safety data on Entereg

Adolor and GlaxoSmithKline have revealed that the FDA is looking for more safety data along with new results for carcinogenicity for the experimental Entereg. The data requests are a condition for the agency's approval to use Entereg as a treatment for post-surgery bowel dysfunction. Originally, Entereg was in trials for opiate-induced constipation, a much larger indication. But those studies were suspended after researchers determined the drug was linked to higher rates of cardiovascular incidents, fractures as well as skin cancers. New data is expected in the third quarter. 

- see this release on Entereg
- read the AP report

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