Charcot-Marie-Tooth disease type 2B1
MONDO:0011569Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy.
Also known as: AR-CMT2B1, CMT2B1, Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA, Charcot-Marie-Tooth disease, type 2B1, LMNA Charcot-Marie-Tooth disease type 2, autosomal recessive Charcot-Marie-Tooth disease type 2B1, autosomal recessive axonal CMT4C1, CMT 2B1
10 clinical trials for this condition and its sub-types, 1 tagged with Charcot-Marie-Tooth disease type 2B1 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
Can tiny cell particles calm a fiery facial nerve?
Symptom relief Recruiting nowResearchers are testing whether exosomes, tiny particles released by donor umbilical cord or placental stem cells, are safe and can help people with trigeminal neuralgia or peripheral neuropathy. The trial enrolls about 20 adults with a confirmed diagnosis. Participants receive t…
Phase 1 • Sponsor: The Foundation for Orthopaedics and Regenerative Medicine • Aim: Symptom relief
Last updated Oct 21, 2026 18:00 UTC
-
800-Patient registry maps the hidden path of rare muscle and heart gene disorders
Knowledge-focused Recruiting nowLaminopathies and emerinopathies are rare disorders caused by mutations in the LMNA or EMD genes, often affecting skeletal muscles and the heart. Researchers at French hospitals are building a registry of 800 patients with confirmed mutations to record detailed genetic, neurologi…
Sponsor: Pitié-Salpêtrière Hospital • Aim: Knowledge-focused
Last updated Sep 23, 2026 00:00 UTC
-
Global registry aims to map the full course of Charcot-Marie-Tooth disease
Knowledge-focused Recruiting nowResearchers are building a global registry to collect patient-reported surveys, genetic test results, and medical records from people with Charcot-Marie-Tooth disease and related inherited neuropathies. The study is open to children and adults with a confirmed or suspected diagno…
Sponsor: Hereditary Neuropathy Foundation • Aim: Knowledge-focused
Last updated Sep 19, 2026 00:00 UTC
-
Scientists hunt for 'Modifier Genes' that could explain why some LMNA patients fare better than others
Knowledge-focused Recruiting nowThis study aims to identify genetic factors that affect how severe muscle and heart problems become in people with LMNA gene mutations. Researchers will collect skin and muscle samples from 40 participants and use advanced DNA and RNA analysis to look for protective or aggravatin…
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:10 UTC
-
4,000 patients to help unlock secrets of nerve disease
Knowledge-focused Recruiting nowThis study is collecting information from 4,000 adults with peripheral neuropathy (nerve damage) to better understand the condition. Researchers will combine standard tests with nerve ultrasound to see if it helps diagnose and track the disease. No new treatments are being tested…
Sponsor: Casa di Cura Dott. Pederzoli • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:08 UTC
-
Liquid nerve biopsy could unlock ALS secrets
Knowledge-focused Recruiting nowThis study is collecting nerve samples and biofluids from 400 people with ALS or peripheral neuropathies to find biological markers for early diagnosis and disease tracking. By analyzing individual cells, researchers hope to identify molecular changes that happen before symptoms …
Sponsor: Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:02 UTC