Crick
HomeTrialsGenesDrugs23andMeGraphBlogContact
  • Home
  • Trials
  • Genes
  • Drugs
  • 23andMe
  • Graph
  • Blog
  • Contact
Crick

An open-source clinical intelligence platform. Explore clinical trials, gene networks, and molecular structures using public data sources.

Data Sources

  • ClinicalTrials.gov
  • OpenTargets
  • ClinVar
  • PubChem

Links

  • Contact
  • About
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “Emery-Dreifuss Muscular Dystrophy”

6 trials

Filters

Phase
Early Phase 1
Phase 1
Phase 2
Phase 3
Phase 4
Status
Recruiting
Active, Not Recruiting
Not Yet Recruiting
Completed
Enrolling by Invitation

Showing 6 of 6 results

Not applicableStudy completedNCT02876809
What this trial is testing

A Model for Healthy Aging: Moscow Centenarians (AGE-100)

Who this might be right for
Aging
Pirogov Russian National Research Medical University 100
Not applicableStudy completedNCT00094393
What this trial is testing

Clinical Studies of Progeria

Who this might be right for
Progeria
National Human Genome Research Institute (NHGRI) 15
Not applicableStudy completedNCT05099107
What this trial is testing

Changes of Motor Function Tests in Congenital Myopathy Subjects Treated With Oral Salbutamol as Compared to no Treatment

Who this might be right for
Congenital MyopathyNeuromuscular DiseasesMusculoskeletal Diseases+3 more
Vastra Gotaland Region 18
Not applicableLooking for participantsNCT03058185
What this trial is testing

Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies)

Who this might be right for
LaminopathiesEmerinopathies
Pitié-Salpêtrière Hospital 800
Not applicableLooking for participantsNCT05394506
What this trial is testing

Modifying Factors in Striated Muscle Laminopathies

Who this might be right for
LaminopathiesEmery Dreifuss Muscular Dystrophy 2LMNA-Related Congenital Muscular Dystrophy+1 more
Institut National de la Santé Et de la Recherche Médicale, France 40
Not applicableLooking for participantsNCT01403402
What this trial is testing

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Who this might be right for
Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) DeficiencyAlpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)+49 more
Cure CMD
4,000