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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:

  1. Diagnosis of Chronic Fatigue Syndrome ( 12 months) as defined by the 1988 CDC case definition of CFS.
  2. Adults 18 to 60 years of age.
  3. Karnofsky Performances Score of 40 to 60 during the 12 weeks immediately preceding the start of the study drug infusions.
  4. 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