Soleno Therapeutics, Inc.

Individuals and families with #PraderWilliSyndrome overcome challenges every day. If you’re living with PWS, share your story of resilience and give hope to others facing this #RareDisease. Share your story here: www.support4pws.com.

Happy 4th of July! To our Redwood City neighbors, we’ll see you at the parade!

We are pleased to announce that Soleno Therapeutics has submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for DCCR (diazoxide choline) extended-release tablets for the treatment of Prader-Willi syndrome (PWS) in individuals four years and older who have hyperphagia. Following the FDA’s designation of DCCR as the first-ever Breakthrough Therapy for PWS, this submission marks a significant milestone in our mission to provide innovative treatments to those in need. DCCR also has Orphan Drug Designation for PWS in the U.S. and E.U., as well as Fast Track Designation in the U.S. Hyperphagia, the hallmark symptom of PWS, is a chronic and life-threatening feeling of intense, persistent hunger, food pre-occupation, and extreme drive to seek and consume food that severely diminish the quality of life for individuals with PWS and their families. Stay tuned for updates as we continue our commitment to improving lives. Read more: https://lnkd.in/gTXcnRpR #SolenoTherapeutics #PraderWilliSyndrome #PWSAwareness Foundation For Prader-Willi Research | Prader-Willi Syndrome Association | USA | International Prader-Willi Syndrome Organisation (IPWSO) | Prader-Willi Syndrome Association UK

People with #PraderWilliSyndrome are resilient, determined, and hopeful – and each one of their amazing stories are important. We’re expanding our #PWSAwareness website as a place to share community stories. If you’re part of the PWS community, we invite you to share your story at www.support4pws.com. 

We are growing our team! As we drive toward the potential approval of our first medicine, we are inspired by the possibility of making a positive impact on the lives of individuals and families facing #PraderWilliSyndrome.If you share our dedication to excellence and our commitment to patients, take a look at our open roles: https://lnkd.in/dWPDf_8r #LifeScienceCareers #BiotechCareers #Hiring

#DidYouKnow that there are #PraderWilliSyndrome advocacy organizations and resources across the globe? Check out the list of International Prader-Willi Syndrome Organisation (IPWSO) members to connect with the global PWS community and find the organizations nearest you: https://lnkd.in/eCpxkZU2

Though #PWSAwarenessMonth has come to an end, those with #PraderWilliSyndrome deserve support and words of kindness 365 days a year! There’s still time to share your message of hope for this beautiful community at www.Support4PWS.com. #PWSAwareness #PraderWilliSyndromeAwareness #RareDisease Foundation For Prader-Willi Research | Prader-Willi Syndrome Association | USA | International Prader-Willi Syndrome Organisation (IPWSO) | Prader-Willi Syndrome Association UK

It was wonderful to see so many iconic locations across the UK #GlowOrangeForPWS last week! We were proud to support Prader-Willi Syndrome Association UK and Foundation for Prader Willi Research UK in raising awareness of #PraderWilliSyndrome and showing support for this #RareDisease community. https://lnkd.in/dC_-c6iz #PWSAwareness #PWSStrongerTogether #GlowOrange #PraderWilliSyndromeAwareness #PWSAwarenessMonth PWS Stronger Together

Today is #GlowOrange Day! 30+ locations across the UK will light up orange to raise awareness and show support for the #PraderWilliSyndrome (PWS) community. See the trail: https://lnkd.in/exNHyAyQ PWS is a complex genetic #RareDisease, and it is estimated that there are about 2,000 people living with PWS in the UK. For those in the UK, you can show your support by taking photos of any of the locations lit up in orange and share your photos to your social media by using #GlowOrangeForPWS and tagging PWS Stronger Together, Prader-Willi Syndrome Association UK, and Foundation for Prader Willi Research UK. We’re looking forward to the event at Battersea Power Station, London – the final stop on the Glow Orange trail! #PWSStrongerTogether

As we near the end of #PraderWilliSyndrome Awareness Month, there are just two more days to join Prader-Willi Syndrome Association UK and Foundation for Prader Willi Research UK in traveling virtually across the UK by logging #MoveItMay minutes. Any type of movement counts! Tomorrow, all the locations we’ve collectively ‘visited’ will #GlowOrangeForPWS! https://lnkd.in/e3VCzKYb