epm Therapeutics

06/15/2026

A breakthrough molecule requires a seasoned team to navigate the complex journey. epm Therapeutics is led by industry veterans with a combined 80+ years of global experience at giants like GSK and Eli Lilly.

Meet the team driving our mission forward: https://bit.ly/EPM_MeetUs

06/12/2026

Are you a caregiver with questions about sleep disorders related to ? TREND Community is hosting a “Shedding Light on PWS and Sleep” webinar on Wednesday, June 17. Hear directly from those living with PWS, as well as cataplexy and clinical experts.

Get more info in the post below ⬇️

Many families living with PWS have questions about sleep, and cataplexy is often one of the most misunderstood symptoms.
Join us for Shedding Light on PWS and Sleep: Understanding Cataplexy, a conversation featuring caregivers, lived experience perspectives, and clinical experts. Together, we'll explore how to recognize cataplexy, better understand its connection to sleep disorders in PWS, and share real-world experiences and practical tips.

🗓️ Wednesday, June 17, 2026
⏰ 2:00–3:30pm ET/1:00-2:30pm CT/12n-1:30pm MT/11:00am-12:30 PT

Whether you're newly learning about cataplexy or looking to connect with others who understand the journey, we hope you'll join us.
RSVP here: https://www.eventcreate.com/e/cataplexy-pws-webinar

06/05/2026

“Be patient. Be calm. Be grateful.”

Wise words from Teri, a mother sharing her son's journey with Prader-Willi syndrome. If you need a reminder to not sweat the small stuff today, read their full story from The Foundation for Prader-Willi Research ⬇️

Teri's son Jacob is 21 years old, happy, healthy and living on his own; as hard as it was to let him go, she gets to watch him be independent.

06/01/2026

On this , we encourage you to check out the epm Therapeutics website!

This is an incredible resource for individuals looking to learn more about:
⬢ Prader-Willi syndrome (PWS)
⬢ Who we are
⬢ What we're researching
⬢ How our EPM301 molecule may one day improve the lives of those impacted by

🔗 Check it out now: https://bit.ly/epm_NewWebsite

05/29/2026

There’s still time to double your impact and have your gift to The Foundation for Prader-Willi Research matched in honor of !

Take a look at some of the inspiring faces of the people their research has touched:

Research is everything to us because behind every study, every grant, and every breakthrough are real people and real moments 🧡

That's why FPWR exists.

We were founded by parents who believed families affected by Prader-Willi syndrome deserved more answers, more options, and more hope for the future. Today, we remain relentlessly focused on research because families deserve better options.

This spring, FPWR awarded more than $1 million in new research grants supporting 7 innovative projects exploring hunger, sleep, behavior, brain pathways, and future therapies for PWS.

Every project adds another piece to the puzzle and another step toward progress.

Throughout PWS Awareness Month, families shared milestone moments big and small:
• A new word
• A better night of sleep
• A glimpse of independence

These moments remind us why research matters.

Thank you for helping move research and hope forward.

Final days to have your gift matched:
https://hubs.la/Q04jd0Ym0

05/26/2026

As we come to the end of Prader-Willi Syndrome Awareness Month, we’re recognizing the resilience, courage and advocacy of the PWS community.

We know that a disease doesn't seem rare if you or a loved one are experiencing it.

At epm Therapeutics, we remain focused on advancing innovation that has the potential to make a meaningful difference for the PWS community.

Get to know our team at https://bit.ly/EPM_MeetUs

05/22/2026

Families affected by Prader-Willi syndrome (PWS) live with daily challenges, including constant hunger and food-seeking behaviors due to hyperphagia. Simple routines and clear food rules are not about restriction — they are about safety, stability, and reducing anxiety for individuals living with PWS.

This graphic from Prader Willi Syndrome Association Ireland (PWSAI) highlights why structure around food is so important, and offers insight into the reality many families navigate every day:

Sometimes what looks like “just one small treat” can create a cycle of expectation, anxiety and distress for a person with PWS.

Every family living with PWS has their own routines, rules and strategies around food, designed to help their child feel safe, secure and happy.

The most supportive thing we can do is respect those routines, even when they may look different from what we’re used to.

Awareness creates understanding and understanding creates compassion.

05/15/2026

Join us as we Go Orange for Prader-Willi Syndrome Awareness Day!

We will be sporting orange in support of those with Prader-Willi syndrome, their friends, families and caregivers who stand beside them every day. Together, we can help raise awareness, foster understanding and advocate for continued research and innovation that brings hope to the PWS community. 🧡

05/13/2026

The epm Therapeutics team is thrilled to welcome Kylie O’Keefe to our Board of Directors!

Kylie brings a wealth of biopharmaceutical experience to our board, including a proven track record in the development and commercialization of products to treat rare diseases.

Her guidance will be invaluable as we advance EPM301 through clinical development as a potentially meaningful new treatment option for people living with .

Get to know Kylie and learn why she’s excited to join our board: https://bit.ly/epm_KylieOKeefe

05/11/2026

On this , we’re highlighting our ongoing work and partnership with Patheon & Thermo Fisher Scientific to advance the oral formulation development of EPM301.

From the very beginning, we've approached this formulation with the needs of the (PWS) community in mind, including:
• A formulation that is low in calories
• A dosage form that is small and easy to swallow
• Convenience for caregivers administering treatment

While our work in the lab is vital, we know the real impact happens beyond it. Every decision we make reflects our commitment to ensuring that each step of development is guided by the real-world needs of PWS patients and their caregivers.

Because innovation isn't just about what we create — it’s about who we create it for.