Research and Clinical Trials Update Meetings
Thursday 11 September 2025, 5pm London, UK time on Zoom
Across the globe, scientists and clinical researchers are working to develop effective treatments and interventions for PWS. As our understanding of this complex genetic condition continues to grow, clinical trials remain essential in transforming research into real-world solutions, helping evaluate the safety, efficacy, and potential impact of new therapies.
IPWSO’s 2025 Research and Clinical Trials Update Meeting will take place on Thursday, 11 September 2025 at 5:00 PM (London, UK time) via Zoom.
📅 Click here to convert to your local time
This annual event brings together leading researchers, clinicians, and members of the global PWS community to share the latest developments in research and clinical trials. Attendees will hear directly from experts about ongoing studies, emerging treatments, and what the future holds for care and intervention in PWS.
Whether you’re a parent or caregiver, a person living with PWS, a healthcare professional, or a researcher, this session is an opportunity to stay informed, ask questions, and be part of the global conversation driving progress in PWS treatment.
What to Expect:
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Presentations from leading scientists and clinicians
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Updates on current and upcoming clinical trials
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Insights into therapeutic advances and genetic research
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Live Q&A session with presenters
More details, including the list of speakers, will be available soon.
Click the “RSVP” button below to let us know you plan on attending, and to add the event to your calendar.

In accordance with our Policy and Code of Practice, IPWSO does not promote individual trials or the use of specific medications.
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International Community
IPWSO was established so that PWS associations, families, clinicians and caregivers around the world could exchange information and support and have a united global voice under one umbrella.
Information for Medical Professionals
The latest medical and scientific research and information, plus guides into common medical issues affecting people with PWS.
What is PWS?

Prader-Willi syndrome is a complex genetic condition. Various studies have shown that between 1 in 15,000 to 25,000 children are born with Prader-Willi syndrome and it affects all races and both sexes equally.
Free Diagnosis

If you suspect your patient has Prader-Willi syndrome, based on the clinical signs and symptoms, but are unable to access testing in your country, then you may be able to access free testing.