Sanofi begins pivotal clinical trial to evaluate therapy for patients at risk of rapidly progressing autosomal dominant polycystic kidney disease (ADPKD)
Autosomal dominant polycystic kidney disease (ADPKD) is a devastating rare genetic kidney condition that leads to the growth of numerous cysts in the kidneys. Affecting an estimated 120,000 people in the U.S. and 170,000 in the European Union, ADPKD becomes so severe for approximately half of those patients that they face either a lifetime of dialysis or a kidney transplant.
Sanofi is beginning a pivotal clinical trial to study the safety, efficacy, and tolerability of an investigational oral agent called venglustat for certain patients with ADPKD. The international trial is enrolling patients who are at risk of rapidly progressive ADPKD.
Genetic mutation leads to devastating condition
ADPKD is caused by a mutation in the PKD1 or PKD2 gene that leads to a build-up of complex substances called glycosphingolipids in the kidneys. Glycosphingolipid accumulation is thought to be an important driver of cyst growth  . Relentless cyst growth can cause chronic pain and lead to reduced kidney function and kidney failure in ADPKD patients. The symptoms of ADPKD usually start to appear between the ages of 30 and 40, but they can begin as early as childhood for some patients .
“The PKD Foundation welcomes research efforts that have the potential to bring new therapies to patients living with this condition,” said David Baron, Ph.D., Chief Scientific Officer of the PKD Foundation. “We appreciate that Sanofi has engaged with the ADPKD patient community throughout the early stages of clinical development for venglustat and look forward to continuing to work with Sanofi.”
Venglustat is an investigational oral therapy designed to inhibit the abnormal accumulation of a substance in the body called glucosylceramide (GL-1), which plays a role in production of glycosphingolipids. In genetic mouse models of ADPKD, inhibition of glycosphingolipid production has been shown to reduce kidney cyst growth . The clinical significance of this is under investigation.
Venglustat has received Orphan Drug designation in the U.S. for the treatment of ADPKD. The ADPKD clinical trial will be conducted at sites in the U.S., Canada, China and Japan as well as several EU countries.