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Comparison of Ro 31-8959 Plus Zidovudine (AZT) Versus AZT Plus Zalcitabine (ddC) Versus Ro 31-8959 Plus AZT Plus ddC

Phase 2
Completed
Conditions
HIV Infections
Registration Number
NCT00001040
Lead Sponsor
Hoffmann-La Roche
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (10)

Univ of Alabama at Birmingham

πŸ‡ΊπŸ‡Έ

Birmingham, Alabama, United States

Stanford Univ Med Ctr

πŸ‡ΊπŸ‡Έ

Stanford, California, United States

Univ of Colorado Health Sciences Ctr

πŸ‡ΊπŸ‡Έ

Denver, Colorado, United States

Northwestern Univ Med School

πŸ‡ΊπŸ‡Έ

Chicago, Illinois, United States

Bellevue Hosp / New York Univ Med Ctr

πŸ‡ΊπŸ‡Έ

New York, New York, United States

Univ of Rochester Med Ctr

πŸ‡ΊπŸ‡Έ

Rochester, New York, United States

Ohio State Univ Hosp

πŸ‡ΊπŸ‡Έ

Columbus, Ohio, United States

Girard Med Ctr

πŸ‡ΊπŸ‡Έ

Philadelphia, Pennsylvania, United States

Univ TX Galveston Med Branch

πŸ‡ΊπŸ‡Έ

Galveston, Texas, United States

Univ of Washington

πŸ‡ΊπŸ‡Έ

Seattle, Washington, United States

Univ of Alabama at Birmingham
πŸ‡ΊπŸ‡ΈBirmingham, Alabama, United States

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