Challenges in drug development for muscle disease: A stakeholders' meeting

Jerry R. Mendell, Cristina Csimma, Craig M. McDonald, Diana M. Escolar, Scott Janis, John D. Porter, Sharon E. Hesterlee, R. Rodney Howell

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Current treatment benefits for patients with muscle disease are limited, but progress in legislative and scientific initiatives have set the stage for the development of new therapies. The MD-CARE Act (Public Law 107-84), which allocates federal resources to muscular dystrophy, was approved by Congress and signed into law by the President of the United States in 2001. This has shifted the emphasis toward translational research. To facilitate a push toward therapy for muscle disorders, the Muscular Dystrophy Association (MDA) sponsored a meeting with representatives from industry, the Food and Drug Administration (FDA), the National Institutes of Health (NIH), and other government agencies and academia. Each contributed in different ways. The FDA helped define the necessary data to support investigational new drug (IND) applications including the design of proof-of-principle studies, outcome measures for clinical trials, and the pathway for developing surrogate measures for fast-tracking promising new drugs. The NIH, other government agencies, and the MDA described potential funding sources for translational research. Industry delineated a complementary role with academia, and academic investigators elucidated the current strengths and weaknesses of available clinical endpoints. The meeting provided a format for communication for diverse disciplines that usually have no common meeting ground, helping to lay the foundation for bringing products to market in a timely fashion.

Original languageEnglish (US)
Pages (from-to)8-16
Number of pages9
JournalMuscle and Nerve
Volume35
Issue number1
DOIs
StatePublished - Jan 2007

Keywords

  • Clinical endpoints
  • Clinical trials
  • Drug development
  • Motor function measures
  • Muscle disease
  • Outcome measures
  • Pediatric Evaluation of Disability Inventory
  • Quantitative muscle testing

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

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  • Cite this

    Mendell, J. R., Csimma, C., McDonald, C. M., Escolar, D. M., Janis, S., Porter, J. D., Hesterlee, S. E., & Howell, R. R. (2007). Challenges in drug development for muscle disease: A stakeholders' meeting. Muscle and Nerve, 35(1), 8-16. https://doi.org/10.1002/mus.20686