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  • Pfizer Early Stage GT

    The study will evaluate the safety and dystrophin expression following gene therapy in boys with Duchenne Muscular Dystrophy (DMD). It is a single-arm, non-randomized, open-label study

    Investigator
    Barry J Byrne
    Ages
    2 Years - 3 Years
    Sexes
    Male
  • VASO-Rex study

    Examining two strategies as potential adjuvant therapies for Duchenne muscular dystrophy (DMD); aerobic exercise training (to induce adaptations in skeletal muscle and improve cardiovascular health) and tadalafil, an FDA-approved vasodilator (to鈥�

    Ages
    6 Years - N/A
    Sexes
    Male
  • Edgewise-210

    The LYNX study is a 2-part, multicenter, Phase 2 study of safety, pharmacokinetics and biomarkers in children with Duchenne muscular dystrophy including a randomized, double-blind, placebo-controlled part A, followed by an open-label part B.

    Ages
    4 Years - 9 Years
    Sexes
    Male
  • Edgewise-215 FOX

    The FOX study is a 2-part, multicenter, Phase 2 study of safety, pharmacokinetics, and biomarkers in children and adolescents with Duchenne muscular dystrophy previously treated with gene therapy including a randomized, double-blind,鈥�

    Ages
    6 Years - 17 Years
    Sexes
    Male
  • Givinostat Long Term Study

    This is an open label, long-term safety, tolerability, and efficacy study of GIVINOSTAT in all DMD (Duchenne's muscular dystrophy) patients who have been previously treated in one of the GIVINOSTAT studies.

    Investigator
    Barry J Byrne
    Ages
    7 Years - N/A
    Sexes
    Male