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| Sponsored by: |
Hemispherx Biopharma |
| Information provided by: | Hemispherx Biopharma |
| ClinicalTrials.gov Identifier: | NCT00215813 |
Purpose
This is an open label study of Ampligen in patients with chronic fatigue syndrome.
| Condition | Intervention | Phase |
|
Chronic Fatigue Syndrome |
Drug: Ampligen (poly I: poly C12U) |
Phase III |
| MedlinePlus related topics: | Chronic Fatigue Syndrome |
| Drug Information available for: | Ampligen |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Expanded Access Assignment, Safety/Efficacy Study |
| Official Title: | An Open Label Study of Ampligen in Chronic Fatigue Syndrome |
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.
Eligibility
| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations| Contact: Sharon Conway | 215-988-0080 | sharon@hemispherx.net |
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Show 51 Study Locations |
| Hemispherx Biopharma |
| Principal Investigator: | Daniel Peterson, M.D. | Sierra Internal Medicine |
| Principal Investigator: | Lucinda Bateman, M.D. | Fatigue Consultation Clinic |
| Principal Investigator: | Charles W. Lapp, M.D. | Hunter-Hopkins Center, P.A. |
More Information
| Study ID Numbers: | AMP 511 |
| First Received: | September 16, 2005 |
| Last Updated: | October 24, 2006 |
| ClinicalTrials.gov Identifier: | NCT00215813 |
| Health Authority: | United States: Food and Drug Administration |
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