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  2. Stamulumab - Wikipedia

    en.wikipedia.org/wiki/Stamulumab

    Stamulumab (MYO-029 [1]) is an experimental myostatin inhibiting drug developed by Wyeth Pharmaceuticals for the treatment of muscular dystrophy (MD). Stamulumab was formulated and tested by Wyeth in Collegeville, Pennsylvania. [2]

  3. Mom Has 3 Days to Get Son Life-Saving Treatment for Muscular ...

    www.aol.com/mom-3-days-son-life-150759249.html

    “Duchenne muscular dystrophy (DMD) is one of the most severe forms of inherited muscular dystrophies,” the National Library of Medicine says. “Mutations in the dystrophin gene lead to ...

  4. Delandistrogene moxeparvovec - Wikipedia

    en.wikipedia.org/wiki/Delandistrogene_moxeparvovec

    Delandistrogene moxeparvovec, sold under the brand name Elevidys, is a recombinant gene therapy used for the treatment of Duchenne muscular dystrophy. [3] It is designed to deliver into the body a gene that leads to production of Elevidys micro-dystrophin that contains selected domains of the dystrophin protein present in normal muscle cells. [3]

  5. Myostatin inhibitor - Wikipedia

    en.wikipedia.org/wiki/Myostatin_inhibitor

    Clinical trials for muscular dystrophy have not proven successful in generating functional improvements compared to placebo. Gains of muscle mass were small to non-existent in this population. [ 13 ] Research is ongoing on the potential use of myostatin inhibitors for motor neuron diseases like spinal muscle atrophy and amyotrophic lateral ...

  6. ICOTF: Targeting Stem Cells for Muscular Dystrophy Treatment

    www.aol.com/news/icotf-targeting-stem-cells...

    By David Bautz, PhD OTC:ICOTF | TSX:MSCL.V Satellos Bioscience Inc. (OTC:ICOTF)(TSX:MSCL.V) is a Canadian biotechnology company dedicated to developing therapies for the treatment of life ...

  7. Cure Rare Disease - Wikipedia

    en.wikipedia.org/wiki/Cure_Rare_Disease

    Finding success in developing a novel framework to treat the first patient, Cure Rare Disease expanded the development of additional therapeutics. Currently, there are 18 mutations and conditions in the Cure Rare Disease pipeline, including Duchenne muscular dystrophy, various subtypes of Limb-girdle muscular dystrophy, spinocerebellar ataxia ...

  8. Austin musician Casey McPherson opens Everlum Bio lab to ...

    www.aol.com/lifestyle/austin-musician-casey...

    Spinal muscular atrophy now has a gene therapy treatment, given shortly after birth to introduce a new copy of the SMN1 gene. Babies now born with SMA are identified at birth and treated within a ...

  9. Physical therapy for Duchenne muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Physical_therapy_for...

    Devices to help a person with duchenne muscular dystrophy stand are a common treatment approach. [3] Orthotic devices are used (as discussed above) and also specific standing devices such as standing frames, standing wheelchairs, and tables that have a tilt function.

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