Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

3 clinical studies listed.

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Muscular Dystrophies (Duchenne, Becker, Myotonic Dystrophy)

Tundra lists 3 Muscular Dystrophies (Duchenne, Becker, Myotonic Dystrophy) clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07608432

Efficacy, Safety, and Tolerability of Zeleciment Rostudirsen (DYNE-251) Administered Intravenously Every 4 Weeks in Ambulatory Participants With Duchenne Muscular Dystrophy (FORZETTO)

The purpose of the study is to assess the efficacy, safety, and tolerability of zeleciment rostudirsen (DYNE-251) administered intravenously (IV) every 4 weeks to ambulatory Duchenne muscular dystrophy (DMD) participants, 4 to 18 years of age, with dystrophin mutations amenable to exon 51 skipping.

Gender: MALE

Ages: 4 Years - 18 Years

Updated: 2026-05-27

1 state

Duchenne Muscular Dystrophy (DMD)
Muscular Dystrophy, Duchenne
Muscular Dystrophy (DMD)
+10
NOT YET RECRUITING

NCT07587242

A Phase 3 Study to Evaluate the Safety and Efficacy of AOC 1044 (Also Referred to as Delpacibart Zotadirsen) in Participants With DMD With Gene Mutations Amenable to Exon 44 Skipping

A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Intravenous AOC 1044 for the treatment of Duchenne Muscular Dystrophy (DMD) with Gene Mutations Amenable to Exon 44 Skipping

Gender: MALE

Ages: 7 Years - 16 Years

Updated: 2026-05-14

Muscular Dystrophies
Muscular Dystrophies (Duchenne, Becker, Myotonic Dystrophy)
Muscular Disorders, Atrophic
+11
ENROLLING BY INVITATION

NCT02413450

Derivation of Human Induced Pluripotent Stem (iPS) Cells to Heritable Cardiac Arrhythmias

Human induced pluripotent stem cells (hiPSCs) have driven a paradigm shift in the modeling of human disease; the ability to reprogram patient-specific cells holds the promise of an enhanced understanding of disease mechanisms and phenotypic variability, with applications in personalized predictive pharmacology/toxicology, cell therapy and regenerative medicine. This research will collect blood or skin biopsies from patients and healthy controls for the purpose of generating cell and tissue models of Mendelian heritable forms of heart disease focusing on cardiomyopathies, channelopathies and neuromuscular diseases. Cardiomyocytes derived from hiPSCs will provide a ready source of disease specific cells to study pathogenesis and therapeutics.

Gender: All

Ages: 18 Years - 85 Years

Updated: 2026-01-16

1 state

Inherited Cardiac Arrythmias
Long QT Syndrome (LQTS)
Brugada Syndrome (BrS)
+7