Janssen's Sirukumab Brings Mortality Imbalance Into FDA Panel Review

Unfavorable trends in all-cause death, malignancy and major adverse cardiovascular events are key safety issues facing US agency's Arthritis Advisory Committee, which also is being asked to weigh adequacy of Janssen's dose selection and, more generally, use of long-term placebo controls in rheumatoid arthritis studies.

More from US FDA Performance Tracker

More from Regulatory Trackers