ALCAP, the Association pour la Lutte Contre l’Alcaptonurie, is the support group for AKU patients and their families in France.
ALCAP aims to:
Provide support to patients and their families
Provide information about AKU and educate health professionals
Promote medical research
Raise funds to achieve these goals
To find out more about ALCAP, visit their website.
ALCAP are a partner in the DevelopAKUre clinical trials, leading on patient support to the French and Belgium patients who are enrolled in the French clinical
site at the Hopital Necker in Paris.
Watch this short video created by ALCAP explaining Alkaptonuria, the AKU Society and our DevelopAKUre clinical trials:
Hi! My name is Maria and I am currently a 2nd-year student at Royal Holloway University of L.. ...more
Today's blog is written by Nick Sireau the Chair and CEO of the AKU Society, It was in.. ...more
We are delighted to announce that all the data from the SONIA 2 clin.. ...more
My name is Alev Sen. I’m the main researcher on a study of treatment for AKU in UK hea.. ...more