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Clinical Trials/PER-017-03
PER-017-03Completed未知

HIV TREATMENT PROTOCOL WITH PEG-INTRON: STUDY SUB-STUDY P00737 AND STUDY P00738

SCHERING PLOUGH DEL PERU S.A.,0 sites0 target enrollmentStarted: March 11, 2003Last updated:

Trial Snapshot

Phase
未知
Status
Completed

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • Subjects must receive a HAART regimen at present.
  • The following laboratory parameters must be met:
  • Platelet count> 75,000/mm3
  • Hemoglobin> 9 gm / dl
  • Absolute neutrophil count> 1,000/mm3
  • Creatinine <1.5 times the upper limit of normal
  • SGOT / SGPT <5 times the normal upper limit

Exclusion Criteria

  • People who are participating in clinical studies of drugs currently in research, or have done so in the previous month.
  • Subjects with a history of hypersensitivity to interferons.
  • Subjects with a history of moderate or severe depression, dementia, or other major psychiatric conditions that require medical treatment.

Investigators

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