A Study of LXR015-1 in HIV-Infected Patients

NCT00002365 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2005-06-24

No results posted yet for this study

Summary

To determine and compare the safety and tolerability of 3 doses of LXR015-1 in HIV-infected patients.

Conditions

  • HIV Infections

Interventions

DRUG

LXR015-1

Sponsors & Collaborators

  • LXR Biotechnology

    lead INDUSTRY

Principal Investigators

  • Bathurst I

Study Design

Purpose
TREATMENT
Masking
NONE

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00002365 on ClinicalTrials.gov