NCT Number: NCT00001040
Comparison of Ro 31-8959 Plus Zidovudine (AZT) Versus AZT Plus Zalcitabine (ddC) Versus Ro 31-8959 Plus AZT Plus ddC
PRIMARY: To determine the efficacy and toxicity of three treatment regimens: saquinavir mesylate (Ro 31-8959) plus zidovudine (AZT) vs. AZT plus zalcitabine (dideoxycytidine; ddC) vs. Ro 31-8959 plus AZT plus ddC.
SECONDARY: To investigate the pharmacokinetics and effects on various clinical parameters of the three regimens.
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Notify MeKey information
Conditions
Age range
13 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Univ of Alabama at Birmingham, Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Prior Medication: Required:
- At least 4 months total of AZT at some point in the past, alone or in combination with other antiretroviral therapy.
Patients must have:
- HIV seropositivity.
- Diagnosis of AIDS, ARC, PGL, or asymptomatic infection.
- CD4 count > 50 to <= 300 cells/mm3.
- Life expectancy of at least 6 months.
- Prior AZT therapy.
Exclusion criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Acute serious opportunistic infections requiring immediate treatment, including (but not limited to) tuberculosis, CMV, cryptococcal meningitis, disseminated MAC, cerebral toxoplasmosis, and Pneumocystis carinii pneumonia.
- Known intolerance to Ro 31-8959, AZT, or ddC.
- Symptoms suggestive of pancreatitis.
- Moderate or severe peripheral neuropathy as evidenced by discomfort from numbness, tingling, burning or pain of the extremities or any related symptoms that are accompanied by an objective finding.
- Visceral Kaposi's sarcoma.
- Lymphoma that will require therapy within the next 6 months.
- Transfusion dependence.
Concurrent Medication:
Excluded:
- Investigational or antineoplastic agents.
Concurrent Treatment:
Excluded:
- Radiotherapy (other than local skin radiotherapy).
- Transfusions.
Prior Medication:
Excluded:
- Any antiretroviral agent (other than AZT) or immunomodulatory therapy within 14 days prior to study entry.
- Prior treatment with an HIV proteinase inhibitor.
Treatment and study plan
Zidovudine
DrugZalcitabine
DrugSponsors and collaborators
Lead sponsor
Hoffmann-La Roche
Industry
Registry information
Official study title
Double-Blind, Randomized, Phase II Study of Ro 31-8959 Plus Zidovudine (AZT) Versus AZT Plus Zalcitabine (Dideoxycytidine; ddC) Versus Ro 31-8959 Plus AZT Plus ddC
Important dates
- Primary completion
- 1994
- First posted
- Aug 31, 2001
- Registry last updated
- Mar 1, 2011
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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