A Clinical Trial of Alternating and Intermittent Regimens of 2',3'-Dideoxycytidine and 3'-Azido-3'-Deoxythymidine in the Treatment of Patients With AIDS and Advanced ARC
NCT ID: NCT00000718
Last Updated: 2021-11-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
112 participants
INTERVENTIONAL
1991-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
AZT extends the survival of some patients with AIDS, and both AZT and ddC are known to inhibit the growth of HIV. When AZT or ddC is given continuously over a prolonged period of time, toxic effects occur that are not found when the drugs are given for 4 - 6 weeks. It is hoped that by alternating the drugs or by giving one drug intermittently, the toxic effects can be decreased without lowering the therapeutic effectiveness of the drugs.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Patients will be assigned to 1 of 7 treatment groups. Both AZT and ddC will be given by mouth every 4 hours. One group will take AZT continuously for 52 weeks. One group will alternate 1 week of AZT with a week with no drug for 48 weeks and another group will alternate 1 week of ddC with a week of no drug for 48 weeks. Other groups will alternate AZT and either low-dose or high-dose ddC on a weekly basis or a monthly basis for 48 weeks. Patients will be seen weekly for the first 8 weeks of study and less often thereafter. Blood samples will be withdrawn frequently and evaluated for possible changes in the immune system, toxic effects, and possible changes in the amount of HIV in the blood. Lumbar punctures and skin biopsies will also be performed.
AMENDED: All patients receiving continuous AZT will be switched to a lower dose of AZT if they have not already been switched. This is in accordance with results of NIAID ACTG 002, 016, and 019 which demonstrate that this dose of AZT delays progression of HIV symptoms.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
TREATMENT
NONE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Zidovudine
Zalcitabine
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Encouraged though not required:
* Inhaled pentamidine as prophylaxis for Pneumocystis carinii pneumonia (PCP).
* Allowed:
* AL-721 use is discouraged but not prohibited.
* Use of aspirin, acetaminophen, and nonsteroidal anti-inflammatory agents should be minimized, with continuous use for \> 72 hours discouraged.
* Acute therapy (7 days) with oral acyclovir.
* Acute therapy with ketoconazole.
Concurrent Treatment:
Allowed:
* Up to 4 units of packed red blood cells for hemoglobin toxicity.
All patients must have the following:
* A consistently positive serum HIV p24 antigen = or \> 70 pg/ml, defined by the Abbott HIV antigen test, on two occasions. The tests must be within 1 month of study entry, separated by at least 72 hours, and the last must be within 2 weeks of starting therapy. Any negative antigen test during the period will exclude the patient from the study.
* A positive antibody to HIV confirmed by any federally licensed ELISA test kit.
* Patients in group A must have AIDS related complex (ARC) as defined by the documented presence of at least one of the following:
* Recurrent oral candidiasis.
* Hairy leukoplakia.
* History of herpes zoster.
* Temperature \> 38.5 degrees C with or without night sweats, persisting for \> 14 consecutive days or \> 15 days in a 30-day interval prior to study entry.
* Weight loss of \> 15 lbs. or 10 percent of body weight noted in a 120-day period prior to study entry.
* Diarrhea defined as = or \> 3 liquid stools per day, persisting for \> 30 days prior to study entry without definable cause.
* Patients in group B must have CDC-defined AIDS not requiring systemic maintenance chemotherapy.
Exclusion Criteria
Patients with the following conditions or symptoms are excluded:
* Transfusion dependence requiring 2 units of blood more than once per month.
* Significant malabsorption (\> 10 percent weight loss within the past 3 months with serum carotene \< 75 IU/ml or vitamin A \< 74 IU/ml).
* Significant cardiac or liver disease.
* Significant neurologic abnormalities defined by any one of the following:
* A significant abnormality on the ddC Neuropathy Targeted Symptom Questionnaire defined as a symptom score \> 4 (moderate severity) in any one of six categories or a score \> 2 (mild severity) in any two of six categories.
* Moderate abnormalities on standardized neurologic exam.
* Any severe abnormality (a value = or \> 4.0) on standardized 4-arm quantitative sensory testing of vibration threshold.
* Diabetes, renal failure, or alcoholism.
* Dose-limiting or transfusion-requiring toxicity during a previous course of zidovudine therapy.
* History of idiopathic thrombocytopenic purpura.
* Requirement for prolonged acyclovir therapy. Patients in group A must not have the following:
* Opportunistic infection or malignancy fulfilling the CDC definition of AIDS.
* Neoplasms other than basal cell carcinoma of the skin or in situ carcinoma of the cervix. Patients in group B must not have the following:
* Active opportunistic infection or AIDS-defining opportunistic infection requiring ongoing systemic therapy and/or prophylaxis other than inhaled pentamidine for Pneumocystis carinii pneumonia prophylaxis.
* Symptomatic visceral Kaposi's sarcoma (KS), progression of KS within the month prior to study entry.
* Concurrent neoplasms other than KS, basal cell carcinoma of the skin or in situ carcinoma of the cervix.
Concurrent Medication:
Excluded:
* Neurotoxic drugs.
* Prolonged acyclovir therapy.
* Antineoplastic therapy.
* Systemic therapy and/or prophylaxis for an AIDS-defining opportunistic infection, other than inhaled pentamidine for Pneumocystis carinii pneumonia (PCP) prophylaxis.
* Other antiretroviral agents, immunomodulators, or systemic corticosteroids.
* Other experimental medication.
Concurrent Treatment:
Excluded:
* Transfusion dependency (requiring 2 units of blood more than once per month).
Prior Medication:
Excluded:
* Antiretroviral agents within 60 days of study entry.
* Biologic modifiers or corticosteroids within 30 days prior to study entry.
* Dideoxycytidine (ddC).
Prior Treatment:
Excluded:
* Blood transfusion within 2 weeks of entry.
Any negative HIV p24 antigen test during the month prior to entry will exclude the patient from the study.
Active drug or alcohol abuse.
13 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hoffmann-La Roche
INDUSTRY
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
G Skowron
Role: STUDY_CHAIR
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Northwestern University CRS
Chicago, Illinois, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Lathey JL, Marschner IC, Kabat B, Spector SA. Deterioration of detectable human immunodeficiency virus serum p24 antigen in samples stored for batch testing. J Clin Microbiol. 1997 Mar;35(3):631-5. doi: 10.1128/jcm.35.3.631-635.1997.
Gries JM, Troconiz IF, Verotta D, Jacobson M, Sheiner LB. A pooled analysis of CD4 response to zidovudine and zalcitabine treatment in patients with AIDS and AIDS-related complex. Clin Pharmacol Ther. 1997 Jan;61(1):70-82. doi: 10.1016/S0009-9236(97)90183-1.
Merigan TC. Treatment of AIDS with combinations of antiretroviral agents. Am J Med. 1991 Apr 10;90(4A):8S-17S. doi: 10.1016/0002-9343(91)90405-m.
Skowron G, Merigan TC. Alternating and intermittent regimens of zidovudine (3'-azido-3'-deoxythymidine) and dideoxycytidine (2',3'-dideoxycytidine) in the treatment of patients with acquired immunodeficiency syndrome (AIDS) and AIDS-related complex. Am J Med. 1990 May 21;88(5B):20S-23S. doi: 10.1016/0002-9343(90)90417-c.
Skowron G, Bozzette SA, Lim L, Pettinelli CB, Schaumburg HH, Arezzo J, Fischl MA, Powderly WG, Gocke DJ, Richman DD, Pottage JC, Antoniskis D, McKinley GF, Hyslop NE, Ray G, Simon G, Reed N, LoFaro ML, Uttamchandani RB, Gelb LD, Sperber SJ, Murphy RL, Leedom JM, Grieco MH, Zachary J, Hirsch MS, Spector SA, Bigley J, Soo W, Merigan TC. Alternating and intermittent regimens of zidovudine and dideoxycytidine in patients with AIDS or AIDS-related complex. Ann Intern Med. 1993 Mar 1;118(5):321-30. doi: 10.7326/0003-4819-118-5-199303010-00001.
Fitzgibbon JE, Howell RM, Schwartzer TA, Gocke DJ, Dubin DT. In vivo prevalence of azidothymidine (AZT) resistance mutations in an AIDS patient before and after AZT therapy. AIDS Res Hum Retroviruses. 1991 Mar;7(3):265-9. doi: 10.1089/aid.1991.7.265.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
11021
Identifier Type: REGISTRY
Identifier Source: secondary_id
ACTG 047
Identifier Type: -
Identifier Source: org_study_id