An Open-Label Treatment Protocol to Provide Continued Elvucitabine Treatment

NCT00675844 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2023-08-14

No results posted yet for this study

Summary

Extension study for participants currently participating in Protocols ACH443-015 and ACH443-018.

Conditions

  • HIV Infections

Interventions

DRUG

Elvucitabine

10 milligrams (mg) elvucitabine daily as part of an ART regimen

Sponsors & Collaborators

  • Achillion, a wholly owned subsidiary of Alexion

    collaborator INDUSTRY
  • Alexion Pharmaceuticals, Inc.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2010-03-31
Completion
2010-03-31

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 NCT00675844 on ClinicalTrials.gov