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OpenTrials
Completed

NCT Number: NCT00002115

A Phase I/II Study of the Safety, Tolerance, and Pharmacokinetics of 9-(2-Phosphonylmethoxyethyl)Adenine ( PMEA; Adefovir ) in Patients With Advanced HIV Disease.

To study the safety, tolerance, pharmacokinetics, and anti-HIV effects of PMEA ( adefovir ) when administered daily by intravenous (IV) and/or subcutaneous (SC) injection in patients with advanced HIV disease.

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Key information

About this study

Patients receive a single IV or SC dose of PMEA daily for 4 weeks. A maximum tolerated dose will be defined for these regimens.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Concurrent Medication:

Allowed:

  • Other antiretroviral therapy IF on a stable dose for at least 4 weeks prior to study entry.
  • Prophylactic therapy with aerosolized pentamidine, oral trimethoprim/sulfamethoxazole (Bactrim, Septra) or dapsone, and fluconazole or ketoconazole IF on a stable prophylactic regimen for at least 4 weeks prior to study entry.

Patients must have:

  • HIV seropositivity.
  • Elevated p24 antigen (> 40 pg/ml).
  • Mean CD4 count <= 100 cells/mm3.
  • Life expectancy of at least 3 months.

Prior Medication:

Allowed:

  • Other prior antiretroviral therapy.
  • Prophylactic therapy with aerosolized pentamidine, oral trimethoprim/sulfamethoxazole (Bactrim, Septra) or dapsone, and fluconazole or ketoconazole.

Exclusion criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Inadequate venous access.
  • Active serious infection (other than HIV infection) requiring parenteral antibiotic therapy.
  • Clinically significant cardiac disease, including symptoms of ischemia, congestive heart failure, or arrhythmia.
  • Psychiatric disturbance or illness that may affect compliance.
  • Malignancy other than Kaposi's sarcoma.

Concurrent Medication:

Excluded:

  • Investigational agents other than stavudine (d4T).
  • Interferon-alpha.
  • Ganciclovir.
  • Foscarnet.
  • Diuretics.
  • Amphotericin B.
  • Aminoglycoside antibiotics.
  • Other nephrotoxic agents.
  • Acyclovir at doses >= 2 g/day.

Prior Medication:

Excluded within 2 weeks prior to study entry:

  • Investigational agents other than stavudine (d4T).
  • Interferon-alpha.
  • Ganciclovir.
  • Foscarnet.
  • Diuretics.
  • Amphotericin B.
  • Aminoglycoside antibiotics.
  • Other nephrotoxic agents.

Excluded within 4 weeks prior to study entry:

  • Systemic therapy for Kaposi's sarcoma. Substance abuse.

Treatment and study plan

Adefovir

Drug

Sponsors and collaborators

Lead sponsor

Gilead Sciences

Industry

Registry information

Important dates

First posted
Aug 31, 2001
Registry last updated
Jun 24, 2005

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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