Subcutaneous IGF-1 is not beneficial in 2-year ALS trial. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Previous human clinical trials of insulin-like growth factor type I (IGF-1) in amyotrophic lateral sclerosis (ALS) have been inconsistent. This phase III, randomized, double-blind, placebo-controlled study was undertaken to address whether IGF-1 benefited patients with ALS. METHODS: A total of 330 patients from 20 medical centers were randomized to receive 0.05 mg/kg body weight of human recombinant IGF-1 given subcutaneously twice daily or placebo for 2 years. The primary outcome measure was change in their manual muscle testing score. Secondary outcome measures included tracheostomy-free survival and rate of change in the revised ALS functional rating scale. Intention to treat analysis was used. RESULTS: There was no difference between treatment groups in the primary or secondary outcome measures after the 2-year treatment period. CONCLUSIONS: Insulin-like growth factor type I does not provide benefit for patients with amyotrophic lateral sclerosis.

publication date

  • November 25, 2008

Research

keywords

  • Amyotrophic Lateral Sclerosis
  • Central Nervous System Agents
  • Insulin-Like Growth Factor I

Identity

PubMed Central ID

  • PMC2617770

Scopus Document Identifier

  • 58149242839

Digital Object Identifier (DOI)

  • 10.1212/01.wnl.0000335970.78664.36

PubMed ID

  • 19029516

Additional Document Info

volume

  • 71

issue

  • 22