Vision
Our vision is a world in which every child with Progeria is cured.
Mission
To discover treatments and the cure for Progeria and its aging-related disorders, including heart disease.
Vision
Our vision is a world in which every child with Progeria is cured.
Mission
To discover treatments and the cure for Progeria and its aging-related disorders, including heart disease.
Progeria is an ultra-rare, fatal, “rapid-aging” disease that afflicts children who, without the FDA-approved treatment lonafarnib, die of heart disease at an average age of 14.5 years. PRF is the only non-profit organization solely dedicated to finding treatments and the cure for Progeria, and is making phenomenal progress toward that goal.

News

PRF Co-Founders Drs. Leslie Gordon and Scott Berns speaking as thought leaders at CiMUS, Spain
The Center for Research in Molecular Medicine and Chronic Diseases (CiMUS) at the University of Santiago in Spain invited PRF co-founders to share their story at a special event on Rare Disease Day 2025.

New clinical trial with the drug Progerinin is officially underway
PRF is thrilled to announce that the first Progerinin clinical trial patient visits are complete!

Get PRF’s 2024 Newsletter here!
PRF’s 2024 Newsletter is OUT – check it out for details on the launch of the NEW Progeria clinical trial, get exciting updates on the lives of those you’re supporting, and SO MUCH MORE.

BIG NEWS: Announcing the launch of a brand-new clinical drug trial!
We’re back at it! PRF is thrilled to announce the start of a new Progeria clinical trial with a new drug called Progerinin.

PRF’s 12th International Scientific Workshop
Join us at our scientific workshop taking place at the Boston Marriott Cambridge Hotel, from October 29-31, 2025, to hear about the latest breakthroughs in Progeria research.
Get Involved
Our lonafarnib clinical trials enrolled 107 children from 42 different countries to test this now-FDA-approved treatment. Because of your support, these children and young adults are living longer, healthier lives.
About PRF
Your donation helps The Progeria Research Foundation treat children with Progeria today, and cure them in the future.
Meet the Kids
We hope their stories inspire you to support PRF, so those dreams can come true.
Events
Team PRF Runs the Falmouth Road Race
August 17, 2025, Falmouth, MA
Details coming soon!
PRF’s 24th Annual International Race for Research
September 13, 2025, Peabody, MA
Details coming soon!
SAVE THE DATE!
Night of Wonder Gala, Westin Boston Seaport District Hotel, Boston, MA
November 14, 2026
Team PRF Runs the Falmouth Road Race
August 17, 2025, Falmouth, MA
Details coming soon!
PRF’s 24th Annual International Race for Research
September 13, 2025, Peabody, MA
Details coming soon!
SAVE THE DATE!
Night of Wonder Gala, Westin Boston Seaport District Hotel, Boston, MA
November 14, 2026