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A Randomized, Double-Blind Active-Controlled, Dose-Ranging Study of the Safety and Efficacy of Chronically Administered MDL 28,574A in the Treatment of HIV-Infected Patients

Phase 2
Completed
Conditions
HIV Infections
Registration Number
NCT00002151
Lead Sponsor
Hoechst Marion Roussel
Brief Summary

To characterize the safety and efficacy of fixed doses of MDL 28,574A administered alone and in combination with zidovudine ( AZT ) in patients with asymptomatic or mildly symptomatic HIV infection. To examine the demographic effects on population pharmacokinetics and pharmacodynamics of MDL 28,574A alone and in combination with AZT.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
200
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 (23)

Clinical Investigations Health Services

πŸ‡ΊπŸ‡Έ

Mobile, Alabama, United States

California Clinical Trials Med Group

πŸ‡ΊπŸ‡Έ

Beverly Hills, California, United States

Southwest Community Based AIDS Treatment Group - COMBAT

πŸ‡ΊπŸ‡Έ

Los Angeles, California, United States

UCSF - San Francisco Gen Hosp

πŸ‡ΊπŸ‡Έ

San Francisco, California, United States

George Washington Univ / Hershey Med Ctr

πŸ‡ΊπŸ‡Έ

Washington, District of Columbia, United States

Community Research Initiative of South Florida

πŸ‡ΊπŸ‡Έ

Coral Gables, Florida, United States

Independent Investigator

πŸ‡ΊπŸ‡Έ

Vero Beach, Florida, United States

North Broward Hosp District

πŸ‡ΊπŸ‡Έ

Fort Lauderdale, Florida, United States

Clinical Research Ctr

πŸ‡ΊπŸ‡Έ

Sarasota, Florida, United States

Ctr for Special Immunology

πŸ‡ΊπŸ‡Έ

Chicago, Illinois, United States

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Clinical Investigations Health Services
πŸ‡ΊπŸ‡ΈMobile, Alabama, United States

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