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Levo Therapeutics, Inc : FDA Grants Priority Review for Levo Therapeutics New Drug Application for LV-101 (Intranasal Carbetocin) for the Treatment of Prader-Willi Syndrome

Levo Therapeutics, Inc : FDA Grants Priority Review for Levo Therapeutics New Drug Application for LV-101 (Intranasal Carbetocin) for the Treatment of Prader-Willi Syndrome
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United statesNorth dakotaKostenloser wertpapierhandelSara cotterPaige rivardFoundation for prader willi researchResearch programsFerring pharmaceuticalsDrug administrationLevo therapeutics incPrader willi syndrome association united statesLevo therapeuticsPriority reviewNew drug applicationPrader willi syndrome association unitedTheresa strong

FDA Grants Priority Review for Levo Therapeutics New Drug Application for LV-101 (Intranasal Carbetocin) for the Treatment of Prader-Willi Syndrome

FDA Grants Priority Review for Levo Therapeutics New Drug Application for LV-101 (Intranasal Carbetocin) for the Treatment of Prader-Willi Syndrome
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United statesNorth dakotaSara cotterPaige rivardFoundation for prader willi researchResearch programsFerring pharmaceuticalsDrug administrationLevo therapeutics incPrader willi syndrome association united statesLevo therapeuticsPriority reviewNew drug applicationPrader willi syndrome association unitedTheresa strongIntranasal carbetocin

Soleno Therapeutics Participates in Prader-Willi Syndrome (PWS) DCCR Town Hall

Soleno Therapeutics Participates in Prader-Willi Syndrome (PWS) DCCR Town Hall April 14, 2021 20:40 ET | Source: Soleno Therapeutics Soleno Therapeutics Redwood City, UNITED STATES REDWOOD CITY, Calif., April 14, 2021 (GLOBE NEWSWIRE) Soleno Therapeutics, Inc. (“Soleno”) (NASDAQ: SLNO), a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, today announced that Anish Bhatnagar, M.D., Chief Executive Officer, participated in a Prader-Willi Syndrome (PWS) DCCR Town Hall on Wednesday, April 14, 2021. The event featured speakers from the PWS community who discussed the challenges of living with PWS, as well as patient and caregiver perspectives on DCCR treatment. Dr. Bhatnagar’s remarks highlighted the unmet medical needs facing PWS patients, the Company’s ongoing commitment to obtaining regulatory approval for DCCR and an outline of the necessary steps to obtain reg

United statesManish bhatnagarBrian ritchieSoleno therapeutics incPrader willi syndrome association united statesLifesci advisorsFoundation for prader willi researchDrug administrationSecurities exchangeChief executive officerPrader willi syndromePrader willi researchPrader willi syndrome associationOrphan drug designationFast track designationDiazoxide choline

Harmony Biosciences Hosts Summit Which Sheds Light on Impact of Sleep Disruption in Rare Diseases

Harmony Biosciences Hosts Summit Which Sheds Light on Impact of Sleep Disruption in Rare Diseases
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United statesJeremy kellyNancy leoneLisa caperelliClara pullenLindsay jesteadtSteve maierJerica kellyTerri jo bichellCasey gormanRebecca kingSharon oshaughnessyPaige rivardChion foundationHypersomnia foundationFoundation for prader willi research

Harmony Biosciences Enrolls First Patient In Phase 2 Trial Evaluating Pitolisant For Excessive Daytime Sleepiness In Patients With Prader-Willi Syndrome

Share this article Share this article PLYMOUTH MEETING, Pa. and CHICAGO, Dec. 15, 2020 /PRNewswire/ Harmony Biosciences Holdings, Inc. ( Harmony ) (Nasdaq: HRMY), a pharmaceutical company dedicated to developing and commercializing innovative therapies for patients living with rare neurological disorders who have unmet medical needs, today announced the first patient has been enrolled in a Phase 2 trial evaluating the safety and efficacy of pitolisant for the treatment of excessive daytime sleepiness (EDS) and other key symptoms in patients with Prader-Willi Syndrome (PWS). We view pitolisant as a portfolio in a product opportunity and are taking a mechanism-based approach to drug development in managing its life cycle with the goal of expanding its clinical utility, said Harmony s Chief Medical Officer, Jeffrey Dayno, M.D. We believe pitolisant could offer an important therapeutic benefit in people living with PWS based on preclinical models of the disorder, pitolisant s

United statesBaylor college of medicineJeffrey daynoNancy leonePaige rivardLisa caperelliJohn walterFoundation for prader willi researchDrug administrationPrader willi syndrome association united statesExchange commissionHarmony biosciences holdings incParagon biosciencesHarmony biosciences holdingsPrader willi syndromeChief medical officer