
Cystinosis Research Network
43323789
1996
Lake Forest, IL 60045 USA
cystinosis.org
CystinosisCRN
CystinosisResearch
More from Lake Forest
TRUE GUIDANCE NFP |
|
Eagle Community Credit Union |
|
Age Well Senior Services, Inc. |
|
Paws for Patrick |
|
Blue Wave Athletics |
Similar social media (2901)
COMMUNITY HEALTH CENTER2903 |
|
TEXAS EARLY MUSIC PROJECT2903 |
|
YWCA BUCKS COUNTY2902 |
|
Fam 1st Family Foundation2903 |
|
Consortium for Public Education2904 |
More Alliance/Advocacy Organizations
National Headache Foundation |
|
Foundation for Women's Cancer |
|
Neurofibromatosis Midwest |
|
Us TOO International, Inc. |
News

Returning for the CRN 2025 Family Conference: Speak Up, Speak Out Workshop Join the Grand Rapids conference for this powerful self-advocacy workshop designed for cystinosis patients ages 13-22. Get ready to share your story through art, writing, and performance while connecting with others in the cystinosis community. đźš…Flight and lodging scholarships for those who qualify âť“For questions, email info@cystinosis.org đź’»Ready to go? Register for the conference here and note your interest in the SUSO program https://tinyurl.com/GR2025reg #cystinosis #SpeakUpSpeakOut #SelfAdvocacy (fb)

A new chapter in cystinosis research has begun. Novartis has officially opened the next phase of its CYStem Phase I/II clinical trial, now enrolling children between 2 and 5 years old diagnosed withnephropathic cystinosis. The study represents a hopeful step forward in the development of anautologous stem cell and gene therapy aimed at addressing cystinosis at its genetic root. You can view the official trial listing here: https://tinyurl.com/d3a53asf This moment is the result of years of work across the cystinosis community—researchers, patients, funders, and families. The foundation for this trial was laid through early and sustained investment in the science by the Cystinosis Research Foundation (CRF). Their support for Dr. Stéphanie Cherqui’s pioneering vision made it possible for the research to progress from the lab to the clinic, culminating in the treatment of adult patients in the earlier phase. Those patients’ willingness to participate—and the encouraging outcomes that followed—have made it possible for this therapy to now be studied in young children. At the Cystinosis Research Network (CRN), we are deeply encouraged by this progress. While our mission is distinct from that of the research funders, we work every day to support families living with cystinosis—connecting them to resources, advocating for their needs, and helping them navigate the realities of life with a rare disease. We know how much this news means to the parents of young children with cystinosis who wonder what options the future might hold. We’re grateful to Novartis for engaging with the cystinosis community in meaningful ways as this trial expands. As always, CRN remains committed to walking alongside families as science moves forward—celebrating progress, holding space for uncertainty, and offering support in every season. This trial represents not only a medical milestone, but also a deeply personal one for so many. Our community continues to move forward—together. (fb)
Nearby
20
4.5
Lake Forest
About the organization
- G01, H01, H80 -
Making Lives Better Starts Here The Cystinosis Research Networks vision is the acceleration of the discovery of a cure development of improved treatments and enhancement of quality of life for those with cystinosis. Support The Cystinosis Research Network offers a variety of educational materials and research articles along with opportunities to connect with others online and inperson. Research The Cystinosis Research Networks vision is the discovery of improved treatments and ultimately a cure for cystinosis. Education and Awareness The Cystinosis Research Network educates the public and professional community about cystinosis is actively involved in the rare disease community and offers educational scholarships to individuals with cystinosis and their siblings.
Alliance/Advocacy Organizations Alliance/Advocacy Organizations Specifically Named Diseases Research