AMP 516
Design:
A Multi-Center, Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of Poly I: Poly C12U (Ampligen®) 400 MG IV Twice Weekly Versus Placebo in Patients with Severely Debilitating Chronic Fatigue Syndrome (CFS)/ Myalgic Encephalomyelitis (ME)
Eligibility:
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 18 to 60 years of age.
- Karnofsky Performances Score of 40 to 60 during the 12 weeks immediately preceding the start of the study drug infusions.
- Able to walk on a moving treadmill for a minimum of 20 seconds.
Status:
TRIAL COMPLETED
Please contact Hemispherx Biopharma in writing for additional information regarding trial locations and site contacts:
| By Fax: |
215-988-1739 |
| By E-Mail: |
trialinfo@hemispherx.net |
| By Mail: |
Hemispherx Biopharma, Inc.
One Penn Center
1617 JFK Blvd., 6th Floor
Philadelphia, PA 19103 |
|