Paroxysmal nocturnal hemoglobinuria 2
MONDO:0014166Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene.
Also known as: PIGT paroxysmal nocturnal hemoglobinuria, paroxysmal nocturnal hemoglobinuria 2, paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutation, paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT, paroxysmal nocturnal hemoglobinuria type 2, PNH2
10 clinical trials for this condition and its sub-types, 0 tagged with Paroxysmal nocturnal hemoglobinuria 2 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
New blood treatment could block zika in transfusions
Disease control OngoingThis study tests a special treatment for red blood cells that aims to kill the Zika virus, making transfusions safer. About 692 people who need blood transfusions will receive either treated or standard blood. The goal is to see if the treated blood works just as well and is safe…
Phase 3 • Sponsor: Cerus Corporation • Aim: Disease control
Last updated Jun 27, 2026 11:03 UTC
-
Scientists hunt for genes behind kidney disease
Knowledge-focused OngoingThis study aims to find the genetic causes of kidney diseases like FSGS and nephrotic syndrome. Researchers will collect saliva and urine samples from up to 2,050 participants, including patients and their family members, as well as healthy volunteers. The goal is to understand w…
Sponsor: Beth Israel Deaconess Medical Center • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:06 UTC