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FDA Approves Once-Nightly Lumryz for Patients With Narcolepsy

The FDA has granted final approval to Lumryz for the treatment of cataplexy or excessive daytime sleepiness in adults with narcolepsy. ....

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FDA Approves Once-Nightly Lumryz for Patients With Narcolepsy

The FDA has granted final approval to Lumryz (sodium oxybate) for the treatment of cataplexy or excessive daytime sleepiness in adults with narcolepsy. ....

Michaelj Thorpy , Wake Disorders Center At Montefiore Medical , Albert Einstein College Of Medicine , Drug Administration , Wakefulness Test , Clinical Global Impression , Symptom Daily , Sleep Wake Disorders Center , Montefiore Medical Center , Albert Einstein College ,

Avadel Pharmaceuticals : Regulation FD Presentation - Form 8-K

Avadel Pharmaceuticals Announces Final FDA Approval of LUMRYZ™ for Extended-Release Oral Suspension as the First and Only Once-at-Bedtime Oxybate for Cataplexy or Excessive Daytime. | May 1, 2023 ....

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FDA Approves Once-at-bedtime Sodium Oxybate with Orphan Drug Exclusivity for Narcolepsy

This marks the first and only FDA-approved once-at-bedtime oxybate for individuals living with narcolepsy. ....

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FDA Gives Final Approval to Sodium Oxybate for Cataplexy or Excessive Daytime Sleepiness in Adults With Narcolepsy

The final approval was based on efficacy and safety data from the phase 3 REST-ON study. ....

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