epm Therapeutics

10/16/2026

We’re excited to hear that The Foundation for Prader-Willi Research is researching an emotional regulation therapy program for the PWS community.

Emotional regulation can be an important part of daily life for individuals with Prader-Willi syndrome (PWS), their families and caregivers. Learn more about this exciting program and the research underway in the video below.

10/14/2026

The Prader-Willi Research Foundation Australia is “Bringing Hope to Life” by raising funds for Prader-Willi syndrome (PWS) research and family support services during Giving Day on October 15.

An estimated 1,500 Australian families are affected by PWS. In this video, Rosemary, whose son Bradley was born with PWS, shares a powerful message: “Don’t lose hope.”

At EPM Therapeutics, we believe hope is an important part of the journey toward better treatments and improved quality of life for people living with PWS and their families. Learn more about PWRFA’s Giving Day and how you can help bring hope to life.

10/12/2026

It's a major for team epm! 🌟 We're proud to finally unveil the posters we presented at The Foundation for Prader-Willi Research's Family Conference and Research Symposium last week.

The posters highlight the latest findings from studies evaluating the safety and pharmacokinetics of EPM301, a potential therapeutic for .

We're particularly proud to call out the safety profile of EPM301 these findings establish, as safety is foundational to our approach as we continue the R&D process.

Check out the full posters here: https://bit.ly/epm_news

10/07/2026

Our team is attending The Foundation for Prader-Willi Research Family Conference and Research Symposium this week and we're looking forward to spending time with the people at the heart of the Prader-Willi syndrome community.

Please stop by and see our team from 5- 7 p.m. today, Wednesday, October 7, during the Poster Session and Reception in the Liberty Ballroom.

We’re looking forward to making new connections at this year’s conference!

10/03/2026

Join Prader-Willi Syndrome Association USA's TREND Community on Thursday, October 15, for “Understanding Hyperphagia: Going Beneath the Surface,” a FREE webinar offered via Zoom.

This webinar will feature individuals living with Prader-Willi syndrome sharing their personal experiences and perspectives on living with hyperphagia — which is one of the key PWS symptoms we're developing EPM301 to treat.

We're looking forward to tuning in and learning more!

When: Thursday, October 15, 2026
12:00 PM PT | 3:00 PM ET

Join TREND Community for a zoom webinar, "Understanding Hyperphagia: Going Beneath the Surface," a conversation centered on the lived experience of hyperphagia. Vanessa, Finn, and Chaz will share what hyperphagia feels like in everyday life, including thoughts and emotions around food, non-visible challenges, and the strategies and support that have helped them.

Moderated by rare disease psychologist Dr. Al Freedman, the conversation will also explore what individuals with PWS wish families, healthcare providers, and others better understood about hyperphagia.

Speakers:
Dr. Al Freedman, Counseling Psychologist and Rare Disease Dad
Vanessa Child, Living with PWS
Finn Schneider, Living with PWS
Chaz Sberna, Living with PWS

Register for this webinar at https://www.eventcreate.com/e/understandinghyperphagia

09/30/2026

There’s a lot of work in caring for someone with Prader-Willi syndrome that the world may never see.

The planning before the day begins. The routines that create stability. The decisions made with safety in mind. The constant advocacy, adjustment and attention to details others may not even notice.

Caregiving is not just about managing what’s in front of you. It’s about anticipating what comes next and doing everything possible to help your loved one thrive.

At epm Therapeutics, we are continually inspired by the dedication of PWS caregivers and we see the commitment behind the scenes!

09/25/2026

epm Therapeutics' President & CEO, Dr. Peter Welburn was incredibly honored to participate in the Prader-Willi Research Foundation Australia's 2026 Prader-Willi Syndrome Research and Family Conference!

Stay tuned for more from the conference — including videos from his panel presentation on turning research insights into actionable treatments for individuals living with .

09/22/2026

Nutrition care plays an important role in supporting people with Prader-Willi syndrome throughout every stage of life. In this episode of Nutrition Pearls: the Podcast, Michael Tan and Dr. Jennifer Miller discuss how to optimize nutrition care for people with PWS from infancy through adolescence.

Listen to the episode to learn more about the role of nutrition in supporting individuals with PWS:

Nutrition Pearls: The Pediatric GI Nutrition Podcast · Episode

09/21/2026

The epm Therapeutics team has 80+ years of collective expertise in R&D, financing, and commercialization and a shared commitment to advancing new treatment possibilities for Prader-Willi syndrome.

Our work is grounded in research, collaboration, and the goal of developing treatment options that may improve quality of life for patients and caregivers.

Meet our team at https://bit.ly/EPM_team

09/18/2026

As Direct Support Professionals Week comes to a close, we want to give a heartfelt shout-out to the professionals who play an essential role in the lives of people with Prader-Willi syndrome.

We appreciate hearing from Nicole Tingley, an experienced DSP in the PWS community, in her blog for Prader-Willi Syndrome Association USA.

She says: "The individuals we serve have taught me more about strength, patience, acceptance, and finding joy than I could ever put into words."

Thank you to all DSPs for your dedication, compassion and commitment to the PWS community!

At PWSA | USA, we know firsthand how essential these professionals are to the lives of children and adults living with Prader-Willi syndrome. DSPs are the backbone of care. They provide more than day-to-day supervision, they ensure dignity, safety, independence, and opportunity for those they support. Working with individuals who have PWS requires a unique combination of compassion, patience, vigilance, and skill. From carefully managing food security, to navigating challenging behaviors, to offering encouragement and joy in daily activities, DSPs make an extraordinary difference every single day.

We encourage our families to celebrate the DSPs in their lives, whether with a thank you note, gift card, flowers, or some other meaningful gesture. Let them know how much you appreciate them!

Nicole Tingley, an experienced DSP in the PWS community, wrote a beautiful blog on what this work means to her. You can read this blog at https://www.pwsausa.org/what-being-a-dsp-means-to-me/