G6PD Deficiency

Join Sanguine's G6PD Deficiency patient community to stay informed on upcoming trials
Join Sanguine's G6PD Deficiency patient community to stay informed on upcoming trials

We Bring Research To You

G6PD deficiency is a genetic disease that happens when the body does not have an adequate amount of glucose-6-phosphate dehydrogenase in the blood, which causes red blood cells to break down. More than 400 million people worldwide are living with G6PD deficiency. Better medicine and treatment options are needed for G6PD deficiency in order to save millions of people each year.

We believe patients like you are the key to making a difference in G6PD deficiency research. Joining a research study can help advance the future of G6PD deficiency 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 not recruiting

Stay in touch and we will let you know when the next recruitment is available.

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!