An Open-Label Study of Poly I: Poly C12U (Ampligen®) in Patients with Severely Debilitating Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (ME). The FDA approved the study for cost recovery. Patients enrolled in the study are responsible for costs related to the therapy, e.g., drug cost, infusion cost, cost of supplies, diagnostic and other laboratory testing.
Subjects who meet the following criteria may be eligible for study participation:
Diagnosis of Chronic Fatigue Syndrome ( 12 months) as defined by the 1988 CDC case definition of CFS
Adults ages 18 to 65 years of age
Karnofsky Performance Score from 20 to 60 during baseline
The study is open to enrollment
Incline Village, NV
Salt Lake City, UT
Please contact Hemispherx Biopharma for additional information regarding trial locations and site contacts:
||Hemispherx Biopharma, Inc.
One Penn Center
1617 JFK Blvd., 6th Floor
Philadelphia, PA 19103