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.

 

Exit mobile version