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Perspectives on clinical trials in spinal muscular atrophy.
Swoboda, Kathryn J; Kissel, John T; Crawford, Thomas O; Bromberg, Mark B; Acsadi, Gyula; D'Anjou, Guy; Krosschell, Kristin J; Reyna, Sandra P; Schroth, Mary K; Scott, Charles B; Simard, Louise R.
Afiliación
  • Swoboda KJ; Department of Neurology, University of Utah School of Medicine, Salt Lake City, Utah 84132, USA. swoboda@genetics.utah.edu
J Child Neurol ; 22(8): 957-66, 2007 Aug.
Article en En | MEDLINE | ID: mdl-17761650
Spinal muscular atrophy is one of the most heterogeneous of the single-gene neuromuscular disorders. The broad spectrum of severity, with onset from the prenatal period to adulthood, presents unique challenges in the design and implementation of clinical trials. The clinical classification of subjects into severe (type 1), intermediate (type 2), and mild (type 3) subtypes has proved useful both in enhancing communication among clinicians internationally and in forging the collaborative development of outcome measures for clinical trials. Ideally, clinical trial design in spinal muscular atrophy must take into account the spinal muscular atrophy type, patient age, severity-of-affection status, nature of the therapeutic approach, timing of the proposed intervention relative to disease progression, and relative homogeneity of the cohort to be studied. Following is an overview of the challenges and opportunities, current and future therapeutic strategies, and progress to date in clinical trials in spinal muscular atrophy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Atrofias Musculares Espinales de la Infancia / Predisposición Genética a la Enfermedad Límite: Child / Humans Idioma: En Revista: J Child Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2007 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Atrofias Musculares Espinales de la Infancia / Predisposición Genética a la Enfermedad Límite: Child / Humans Idioma: En Revista: J Child Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2007 Tipo del documento: Article País de afiliación: Estados Unidos