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Clinical Trials/NCT00002210
NCT00002210
Completed
Phase 2

Phase II Study of the Safety, Tolerance, Pharmacokinetics, and Antiviral Effect of Delavirdine Mesylate (Rescriptor), in Combination With Nucleoside Reverse Transcriptase Inhibitors, in HIV-1-Infected Neonates, Infants, and Children

Pharmacia and Upjohn1 site in 1 country24 target enrollmentAugust 31, 2001

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
HIV Infections
Sponsor
Pharmacia and Upjohn
Enrollment
24
Locations
1
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

The purpose of this study is to see if it is safe and effective to give delavirdine mesylate (Rescriptor) plus two nucleoside reverse transcriptase inhibitors (NRTIs) to HIV-infected children and babies. This study also examines how the body processes Rescriptor when taken with 2 NRTIs.

Registry
clinicaltrials.gov
Start Date
August 31, 2001
End Date
TBD
Last Updated
20 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Pharmacia and Upjohn

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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