epm Therapeutics

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.

05/08/2026

This May during PWS Awareness Month, gifts to The Foundation for Prader-Willi Research will be matched dollar for dollar, up to $25,000!

Research funding is critical to advancing our understanding of PWS and developing therapies that can improve quality of life for individuals living with this complex disorder.

Research is moving PWS forward 🧡
Donations MATCHED for PWS Awareness Month!

Give now: https://hubs.la/Q04dM2Q90

05/07/2026

Get your steps in this month! 👟 In observance of , Prader-Willi Research Foundation Australia is inviting the community to get behind a shared goal: 1,500km for Prader-Willi syndrome research.

Every step counts! Join us as we help raise awareness and funds for research that can change lives for those with PWS.

Learn more, submit your steps and raise money at https://bit.ly/15K_AU.

1500k this May for PWS Research

05/05/2026

Has your loved one been diagnosed with Prader-Willi syndrome? You're not alone.
As we commemorate , we invite you to take the time to watch this incredible video from Prader-Willi Syndrome Association USA, featuring the organization's Adults with PWS Advisory Board sharing advice for family members of children recently diagnosed with PWS.

05/01/2026

May is Awareness Month.

At EPM Therapeutics, our work is driven by a commitment to developing therapies that address the complex needs of individuals living with PWS and support the families and caregivers who stand beside them every day.

While PWS only occurs in approximately 1 in 15,000 births, we know that a disease doesn't seem rare if you or a loved one are experiencing it.

Together, we can help bring greater understanding, urgency, and hope to those affected by PWS.

04/28/2026

May is Prader-Willi Syndrome Awareness Month — and with that in mind, we're shining a spotlight on our friend Becca of Raising Lazarus - PWS as she chronicles her experiences raising a son with PWS and shares plenty of incredible resources along the way.

Be sure to check out her content and give her a follow!