CMT: Clinical Trials

6 trials for CMT, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

3 completed, 3 recruiting. 1 Phase 1, 1 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 11Completed 1
Phase 21Completed 1

Follow CMT: new trials by email Literature Review of CMT trials Research Report on CMT

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Multi-omic Approach to the Identification of Novel Biomarkers in Early Charcot-Marie-Tooth 1A Disease (CMT1A)
CMT, CMT (Charcot Marie Tooth Disease)
RecruitingUniversity Medical Center Goettingen702025-03-242026-04-13
TREMOR IN CHARCOT-MARIE-TOOTH
CMT, CMT (Charcot Marie Tooth Disease)
RecruitingUniversity Medical Center Goettingen752024-07-302026-05-06
The Safety and Tolerability of Engensis (VM202) in Patients With Charcot-Marie-Tooth Disease Subtype 1A (CMT1A)
Engensis (VM202) - CMT
Phase 1 / Phase 2CompletedHelixmith Co., Ltd.122020-09-212025-10-06
Analysis of Pain and Quality of Life in Patients With Charcot-Marie-Tooth Neuropathy (CMT)
CMT
CompletedUniversity Medical Center Goettingen2002019-06-032020-11-05
LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies
Leukodystrophy, White Matter Disease
CompletedChildren's Hospital of Philadelphia2362017-01-062025-11-10
The Myelin Disorders Biorepository Project
Leukodystrophy, White Matter Disease
RecruitingChildren's Hospital of Philadelphia120002016-12-082025-10-23

Narrower conditions

Charcot-Marie-Tooth Disease (4)  ·  Adrenoleukodystrophy (2)  ·  Aicardi-Goutieres syndrome (2)  ·  Alexander Disease (2)  ·  Alexanders leukodystrophy (2)  ·  Allan-Herndon-Dudley syndrome (2)  ·  Attention Deficit Disorder with Hyperactivity (2)  ·  CADASIL (2)  ·  Canavan Disease (2)  ·  Cockayne Syndrome (2)  ·  Gangliosidoses (2)  ·  Gangliosidoses, GM2 (2)  ·  Leukodystrophy, Globoid Cell (2)  ·  Leukodystrophy, Hypomyelinating, 5 (2)  ·  Leukodystrophy, Hypomyelinating, 6 (2)

Broader conditions

Congenital Abnormalities (4)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Genetic Diseases, Inborn (4)  ·  Hereditary Sensory and Motor Neuropathy (4)  ·  Heredodegenerative Disorders, Nervous System (4)  ·  Nervous System Diseases (4)  ·  Nervous System Malformations (4)  ·  Neurodegenerative Diseases (4)  ·  Neuromuscular Diseases (4)  ·  Peripheral Nervous System Diseases (4)  ·  Polyneuropathies (4)  ·  Abnormalities, Multiple (2)  ·  Adrenal Gland Diseases (2)  ·  Adrenal Insufficiency (2)  ·  Arthritis (2)

Sponsors

University Medical Center Goettingen (3)  ·  Children's Hospital of Philadelphia (2)  ·  Helixmith Co., Ltd. (1)

Countries

Germany (3)  ·  United States (2)  ·  South Korea (1)

Top investigators

Adeline Vanderver, MD (2)  ·  Michael W Sereda (1)

Results publications

PMID 32342562, PMID 32749716, PMID 41787447

NIH funding

U01NS106845 (1), U54NS115052 (1)