Abstract
To test the safety and efficacy of recombinant human insulin-like growth factor-I (rhIGF-I) in ALS, 183 patients from eight European centers were randomized to receive double-blind placebo (n = 59) or rhIGF-I 0.1 mg/kg/day (n = 124) subcutaneously for 9 months. At study completion, the primary efficacy outcome measure (change in disease progression as assessed by the Appel ALS rating scale) showed no significant difference between treatment groups. RhIGF-I appeared to be safe and well-tolerated.
Original language | English |
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Pages (from-to) | 583-586 |
Number of pages | 4 |
Journal | Neurology |
Volume | 51 |
Issue number | 2 |
Publication status | Published - Aug 1998 |
ASJC Scopus subject areas
- Neuroscience(all)