Pharmaceutical Business review

J&JPRD AF drug gets FDA Advisory Committee recommendation

The recommendation is based on the results from a double-blind Rocket AF Phase 3 trial which showed that once-daily rivaroxaban had a 21% relative risk reduction in stroke and non-CNS systemic embolism while on-treatment compared to warfarin, with low and comparable bleeding rates

The committee voted 9-2 in favor of rivaroxaban in patients with AF who are at risk of stroke and systemic embolism.

J&JPRD Cardiovascular and Metabolism Global Therapeutic Area head peter DiBattiste said they look forward to working with the FDA to help make this important therapy available in the US.