Breaking News

Johnson & Johnson’s SPRAVATO Approved as Standalone Treatment for MDD

FDA approval was supported by positive results from a randomized, double-blind, multicenter, placebo-controlled study.

Author Image

By: Charlie Sternberg

Associate Editor

The U.S. Food and Drug Administration (FDA) has approved a supplemental New Drug Application (sNDA) for Johnson & Johnson’s SPRAVATO (esketamine) CIII nasal spray, making the treatment the first and only monotherapy for adults living with major depressive disorder (MDD) who have had an inadequate response to at least two oral antidepressants. “Treatment-resistant depression can be very complicated, especially for patients who do not respond to oral antidepressants or cannot tolerate...

Continue reading this story and get 24/7 access to Contract Pharma for FREE


Already a subscriber? Sign in

Keep Up With Our Content. Subscribe To Contract Pharma Newsletters