The Safety and Effectiveness of Adefovir Dipivoxil in the Treatment of HIV-Infected Patients

Completed · Phase 3 · Has a placebo group

Conditions studied: Cytomegalovirus Infections, HIV Infections

In brief

To evaluate the safety and efficacy of adefovir dipivoxil in prolonging survival of patients with advanced HIV disease. In CMV prophylaxis substudy: To evaluate the efficacy of adefovir dipivoxil in preventing the development of CMV end-organ disease in patients with advanced HIV coinfected with CMV. The optimal treatment for HIV infection and the prevention of CMV disease has not been identified. Currently available antiretroviral therapies are hampered by both significant toxicities and the development of resistance. In addition, agents for preventing CMV disease, such as oral ganciclovir, are complicated by poor bioavailability and decreased compliance secondary to toxicities. Moreover, discordant results have been reported regarding the effectiveness of oral ganciclovir for preventing CMV disease. There is a need for newer agents with anti-HIV and anti-herpesvirus activity that have good pharmacokinetic and safety profiles and that will be well tolerated by patients. Adefovir dipivoxil is an oral pro-drug of PMEA, a nucleoside analog with activity against a broad spectrum of retroviruses and herpesviruses, including important human pathogens, such as HIV-1, HIV-2 and CMV. Due to its anti-HIV and anti-herpesvirus activity, adefovir dipivoxil may be able to decrease the incidence of opportunistic herpesvirus infections and prolong survival in patients with advanced HIV infection.

Key facts

Study ID

NCT00001082

Run by

National Institute of Allergy and Infectious Diseases (NIAID)

People needed

505

Starts

1996-12-01

Expected to finish

1999-08-01

Last updated by the study team

2013-10-01

Who can join

Age: 13 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Concurrent Medication:
• Allowed:
• Chronically administered concomitant therapies for HIV and opportunistic diseases, including chemotherapy for cutaneous Kaposi's sarcoma, must be on these therapies for at least 30 days prior to study entry.
• Short courses of oral antibiotics or other therapies given for a limited period of 3 weeks.
• Episodic use of IV acyclovir or oral acyclovir > 1g/day for treatment of acute illness is permitted at the clinician's discretion.
• Patients must have:
• A working diagnosis of HIV infection based on the patient's medical history, behavioral history, clinical signs and symptoms, or results of other laboratory tests.
• CD4+ cell count <= 100 cells/mm3 within 60 days prior to randomization (OR, AS PER AMENDMENT 8/7/97, a CD4+ cell count that is both > 100 and <= 200 cells/mm3 within 60 days prior to randomization and a documented nadir CD4+ cell count <= 50 cells/ mm3 at any time prior to randomization).
• Reasonably good health.
• Life expectancy of at least 6 months.
• Access to a refrigerator for the storage of adefovir dipivoxil.
• Signed informed consent from parent or legal guardian for patients less than 18 years of age.
• AS PER AMENDMENT 8/7/97:
• CMV serology (IgG) positive (CMV bDNA cohort and CMV-virology cohort).

You may not qualify if…

• Co-existing Condition:
• Patients with the following symptoms and conditions are excluded:
• Evidence of active CMV disease at screening.
• Conditions that would require use of medications listed in Exclusion Concurrent Medications.
• Concurrent Medication:
• Excluded:
• Any investigational anti-CMV agent.
• Adenine arabinoside (vidarabine).
• Amantadine hydrochloride (Symmetrel).
• Cidofovir (Vistide).
• CMV hyperimmune globulin.
• Cytosine arabinoside (cytarabine).
• Famciclovir.
• Foscarnet (phosphonoformic acid).
• Ganciclovir (Cytovene).
• GW 1263W94 (Benzamidazole).
• Idoxuridine.
• Intravenous acyclovir.
• ISIS 2922 (Anti-sense).
• Lobucavir.
• MSL109.
• Oral acyclovir > 1 g/day.
• Valacyclovir.
• Patients with the following prior conditions are excluded:
• History of CMV end-organ disease.

Where it is running

• Community Consortium / UCSF — San Francisco, California, United States
• Denver CPCRA / Denver Public Hlth — Denver, Colorado, United States
• Washington Reg AIDS Prog / Dept of Infect Dis — Washington D.C., District of Columbia, United States
• AIDS Research Consortium of Atlanta — Atlanta, Georgia, United States
• AIDS Research Alliance - Chicago — Chicago, Illinois, United States
• Louisiana Comm AIDS Rsch Prog / Tulane Univ Med — New Orleans, Louisiana, United States
• Wayne State Univ - WSU/DMC / Univ Hlth Ctr — Detroit, Michigan, United States
• Henry Ford Hosp — Detroit, Michigan, United States
• Southern New Jersey AIDS Cln Trials / Dept of Med — Camden, New Jersey, United States
• North Jersey Community Research Initiative — Newark, New Jersey, United States
• Partners in Research / New Mexico — Albuquerque, New Mexico, United States
• Harlem AIDS Treatment Grp / Harlem Hosp Ctr — New York, New York, United States
• The Research and Education Group — Portland, Oregon, United States
• Philadelphia FIGHT — Philadelphia, Pennsylvania, United States
• Richmond AIDS Consortium / Div of Infect Diseases — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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