Please sign in to follow a disease.
Achromatopsia 3
MONDO:0009875Any achromatopsia in which the cause of the disease is a mutation in the CNGB3 gene.
Also known as: ACHM3, CNGB3 achromatopsia, achromatopsia 3, achromatopsia caused by mutation in CNGB3, achromatopsia type 3, ACHM1 (formerly), ACHM1, formerly, RMCH1 (formerly)
30 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
New wearable gadget aims to give Low-Vision users a helping hand
Symptom relief Not yet recruitingThis study explores how visual impairment affects movement and daily activities, and tests a wearable system called VIS4ION that provides audio and touch cues to help users navigate. Researchers will enroll 150 adults with visual impairment and healthy controls to see if the devi…
Phase: NA • Sponsor: NYU Langone Health • Aim: Symptom relief
Last updated Jun 27, 2026 09:09 UTC
-
New eye camera could spot retinal disease earlier
Knowledge-focused Not yet recruitingThis study will test a new, noninvasive camera called XyCAM CRE that measures blood flow in the back of the eye. Researchers will compare its images with standard eye tests in 350 adults with retinal disorders. The goal is to see if this camera can provide extra information to he…
Sponsor: Stuart Terry Eye Associates • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:07 UTC
-
Gene therapy readiness check: new study maps virus immunity in muscle disease patients
Knowledge-focused Not yet recruitingThis study will test blood samples from 450 people aged 6 to 60 with inherited neuromuscular diseases to see if they have antibodies that could block gene therapy viruses (AAVs). The goal is to understand how common these antibodies are and which patients might be good candidates…
Phase: NA • Sponsor: Genethon • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:04 UTC