Jazz Pharmaceuticals’ Sunosi (solriamfetol) Receives FDA’s Approval for the Treatment of Sleep Disorders
Shots:
- The approval is based on P-III TONES study assessing Sunosi (solriamfetol) vs PBO in 900 patients with excessive daytime sleepiness associated with narcolepsy or Obstructive Sleep Apnea (OSA)
- The P-III TONES study results: @12wks. improvement in PGIc scale (68-74% receiving 75mg & 78-90% receiving 150mg); improvement in wakefulness (assessed in the maintenance of wakefulness test)
- Sunosi (75mg & 150mg for narcolepsy) (37.5 mg, 75 mg &150 mg for OSA) is a NDRI inhibitor, developed and commercialized by Jazz (Ex. Asia) and has received FDA’s ODD for narcolepsy in the US
Click here to read full press release/ article | Ref: Jazz Pharmaceuticals | Image:Cronin Movers Group