Last updated on April 2017

Safety and Biomarker Study of EPI-589 in Subjects With ALS


Brief description of study

Open label study with EPI-589 and ALS subjects

Detailed Study Description

Open label with 30-day run in phase to establish baseline parameters and a 90-day withdrawal phase to determine duration of treatment response.

Clinical Study Identifier: NCT02460679

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Robert Baloh, MD, PhD

Cedar's Sinai
Los Angeles, CA United States
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Robert Miller, MD

California Pacific Medical Center
San Francisco, CA United States
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Kimberly Goslin, MD, PhD

Providence Brain and Spine Institute ALS Center
Portland, OR United States
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