A Pilot Study of the Efficacy of Recombinant Alpha Interferon (IFN-A2b) and Zidovudine (AZT) in the Treatment of Progressive Multifocal Leukoencephalopathy (PML) Complicating HIV-1 Infection
This study has been completed.
Sponsor:
University of Miami
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002270
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: March 1991
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Purpose
To study the effectiveness of alpha interferon (IFN-A2b) and zidovudine (AZT) in treating progressive multifocal leukoencephalopathy (PML) as a complication of HIV-1 infection.
| Condition | Intervention |
|---|---|
|
HIV Infections Leukoencephalopathy, Progressive Multifocal |
Drug: Interferon alfa-2b Drug: Zidovudine |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
| Official Title: | A Pilot Study of the Efficacy of Recombinant Alpha Interferon (IFN-A2b) and Zidovudine (AZT) in the Treatment of Progressive Multifocal Leukoencephalopathy (PML) Complicating HIV-1 Infection |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by NIH AIDS Clinical Trials Information Service:
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
Patients must have:
- HIV seropositivity by both ELISA and Western blot.
- Biopsy proven progressive multifocal leukoencephalopathy (PML).
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
- Intolerant to interferon.
- Prior or concomitant central nervous system disease (CNS) such as toxoplasmosis, multiple sclerosis (MS), or neurosyphilis.
Patients with the following are excluded:
- Intolerant to interferon.
- Prior or concomitant central nervous system disease (CNS) such as toxoplasmosis, multiple sclerosis (MS), or neurosyphilis.
Prior Medication:
Excluded:
- Patients receiving interferon for other reasons.
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00002270 History of Changes |
| Other Study ID Numbers: | 074A |
| Study First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NIH AIDS Clinical Trials Information Service:
|
Leukoencephalopathy, Progressive Multifocal Interferon Alfa-2b Drug Evaluation Acquired Immunodeficiency Syndrome Zidovudine |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Leukoencephalopathy, Progressive Multifocal Leukoencephalopathies Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases Encephalitis, Viral Encephalitis |
Central Nervous System Viral Diseases Polyomavirus Infections DNA Virus Infections Brain Diseases Central Nervous System Diseases Nervous System Diseases Central Nervous System Infections Demyelinating Diseases Interferon-alpha Interferon Alfa-2a Interferon Alfa-2b Interferons Zidovudine Reaferon Antiviral Agents |
ClinicalTrials.gov processed this record on May 16, 2013