Fabry Disease

Join Sanguine's Fabry Disease patient community to stay informed on upcoming trials
Join Sanguine's Fabry Disease patient community to stay informed on upcoming trials

We Bring Research To You

Fabry Disease is a rare genetic disorder that prevents the body from breaking down a type of fat called GL-3 (globotriaosylceramide). Better medicine and treatment options are needed for Fabry disease in order to save thousands of people each year.

We believe patients like you are the key to making a difference in Fabry disease research. Joining a research study can help advance the future of Fabry disease research and impact the development of new treatments and cures.

Sanguine's unique model alleviates many of the difficulties associated with clinical trials and we make it easy for patients to contribute to research for medical conditions that matter most to them, regardless of their location or ability to travel. Sign up to learn more and participate today!

Sanguine's Expertise in Accelerating Research

25,000+
Members in
our community
3
Average # of times a
member has participated
500+
Studies completed
by Sanguine

We are currently recruiting for 1 Fabry Disease study

STUDY NAME:

Fabry Disease At-Home Research Study

compensation:

$50

description

Volunteers with Fabry Disease are needed to participate in a research study from the comfort of their own home. The goal of this research is to develop new diagnostic and treatment options for patients living with Fabry Disease by analyzing biomarkers such as genetic, environmental, and microbial factors that may influence the disease's development.

location

United States

RECRUITMENT FOR THIS STUDY CLOSES IN:
THE STUDY IS NOW CLOSED

Nationwide Partners

We partner with like-minded organizations and nonprofits to connect with patients who want to contribute and help accelerate research.

Join the Sanguine community!