A Phase 2 interventional study of Saquinavir and Zalcitabine in HIV Infections, sponsored by Hoffmann-La Roche. Completed at 47 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2005-06-24.
Sponsored by Hoffmann-La Roche · Phase 2, Interventional, and Treatment
To compare the safety, tolerance, and efficacy of saquinavir mesylate (Ro 31-8959) alone, zalcitabine (dideoxycytidine; ddC) alone, and both in combination, in patients discontinuing or unable to take zidovudine (AZT).
Patients are randomized to one of three treatment regimens: ddC alone, Ro 31-8959 alone, and ddC plus Ro 31-8959. Treatment continues for at least 48 weeks. Patients are stratified by baseline CD4 count. (Per 09/26/94 amendment, a fourth arm, lower dose Ro 31-8959 plus ddC, was discontinued.)
6,687 studies on the registry are indexed under Infections; 807 are open to participants now.
This study's enrollment of 900 is above the median of 120 across 4,200 interventional studies indexed under Infections.
Browse Infections studies →Hoffmann-La Roche is the lead sponsor of 2,061 studies on the registry; 85 are open to participants now.
Of its 319 completed or terminated interventional studies of FDA-regulated products, 239 (75%) have results posted.
Counted across the registry records on this site, refreshed daily.
Concurrent Medication:
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Concurrent Treatment:
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Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
Concurrent Medication:
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Concurrent Treatment:
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Patients with the following prior conditions are excluded:
Prior Medication:
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Prior Treatment:
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This study is completed, as verified in Feb 1995. You cannot join it, but the record below documents what was studied.
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Hoffmann-La Roche