The Safety and Effectiveness of Zidovudine Plus Adefovir in HIV-Infected Patients
This study has been completed.
Sponsor:
Gilead Sciences
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002326
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: October 1995
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Purpose
To study the safety, tolerance, pharmacokinetics, and anti-HIV effects of combination zidovudine (AZT) and PMEA (adefovir) therapy.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Adefovir Drug: Zidovudine |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Pharmacokinetics Study Primary Purpose: Treatment |
| Official Title: | A Phase I/II Study of the Safety, Tolerance, and Pharmacokinetics of Combination Zidovudine (AZT) and 9-(2-Phosphonylmethoxyethyl)Adenine (PMEA; Adefovir) Treatment in HIV-Infected Patients |
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 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
Concurrent Medication:
Allowed:
- Prophylactic therapy with aerosolized pentamidine, oral trimethoprim/sulfamethoxazole (Bactrim, Septra) or dapsone, and fluconazole or ketoconazole IF on a stable regimen for at least 4 weeks prior to study entry.
Patients must have:
- HIV seropositivity.
- Mean CD4 count <= 500 cells/mm3.
- Been receiving AZT at 500 mg daily for at least 4 weeks prior to study entry.
- Life expectancy of at least 3 months.
NOTE:
- Kaposi's sarcoma is permitted provided patient has not received any systemic therapy for KS within the past 4 weeks. Patients with a history of another malignancy must be disease free for 6 months or more prior to study entry.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Inadequate venous access.
- Active, serious infections (other than HIV infection) requiring parenteral antibiotic therapy.
- Clinically significant cardiac disease, including symptoms of ischemia, congestive heart failure, or clinically significant arrhythmia.
- Active malignancy other than Kaposi's sarcoma.
- Mental incapacity or illness that may affect compliance.
Concurrent Medication:
Excluded:
- ddI or ddC.
- Interferon alpha.
- Ganciclovir.
- Foscarnet.
- Diuretics.
- Investigational agents including d4T.
- Chemotherapeutic agents.
- Amphotericin B.
- Aminoglycoside antibiotics.
- Other nephrotoxic agents.
- Immunomodulatory agents.
- Parenteral therapy for an active, serious infection (other than HIV infection).
Prior Medication:
Excluded within 2 weeks prior to study entry:
- ddI or ddC.
- Interferon alpha.
- Ganciclovir.
- Foscarnet.
- Diuretics.
- Investigational agents including d4T.
- Chemotherapeutic agents.
- Amphotericin B.
- Aminoglycoside antibiotics.
- Other nephrotoxic agents.
- Immunomodulatory agents.
Excluded within 4 weeks prior to study entry:
Systemic therapy for Kaposi's sarcoma.
Required:
- AZT at a stable dose for at least 4 weeks prior to study entry. Current use of illicit drugs (e.g., heroin or cocaine). Ingestion of substantial alcohol.
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00002326 History of Changes |
| Other Study ID Numbers: | 217B, GS-93-204 |
| 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:
|
Drug Therapy, Combination Acquired Immunodeficiency Syndrome AIDS-Related Complex |
Antiviral Agents Zidovudine Adenine |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome 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 Zidovudine Adefovir dipivoxil |
Adefovir Antimetabolites Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Reverse Transcriptase Inhibitors Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Therapeutic Uses Anti-HIV Agents |
ClinicalTrials.gov processed this record on May 19, 2013