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A Double-Blind, Randomized, Comparative Study of Delavirdine Mesylate (U-90152S) in Combination With Didanosine (ddI) Versus ddI Alone in HIV-1 Infected Individuals With CD4 Counts of <= 300/mm3

Phase 3
Completed
Conditions
HIV Infections
Registration Number
NCT00002123
Lead Sponsor
Pharmacia and Upjohn
Brief Summary

To evaluate the safety, tolerance, pharmacokinetics, and efficacy of delavirdine mesylate (U-90152S) in combination with didanosine (ddI) versus ddI alone in HIV-positive patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
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 (84)

Univ of Alabama at Birmingham

πŸ‡ΊπŸ‡Έ

Birmingham, Alabama, United States

East Bay AIDS Ctr

πŸ‡ΊπŸ‡Έ

Berkeley, California, United States

California Med Research Group

πŸ‡ΊπŸ‡Έ

Fresno, California, United States

Los Angeles County - USC Med Ctr

πŸ‡ΊπŸ‡Έ

Los Angeles, California, United States

Los Angeles County / Health Research Assoc / Drew Med Ctr

πŸ‡ΊπŸ‡Έ

Los Angeles, California, United States

CARE Ctr / UCLA Med Ctr

πŸ‡ΊπŸ‡Έ

Los Angeles, California, United States

UCI Med Ctr

πŸ‡ΊπŸ‡Έ

Orange, California, United States

AIDS Community Research Consortium

πŸ‡ΊπŸ‡Έ

Redwood City, California, United States

UCD Med Ctr / AIDS and Related Disorders Clinic

πŸ‡ΊπŸ‡Έ

Sacramento, California, United States

St Lukes Medical Group

πŸ‡ΊπŸ‡Έ

San Diego, California, United States

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

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