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A Study of the Immunogenicity of M. Bovis BCG, Delivered Intradermally in Healthy Volunteers

NCT00480688 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2007-05-31

No results posted yet for this study

Summary

To assess the immunogenicity of M. bovis BCG, given intrademally in the standard dose used in clinical practice and to measure the development of the immune response in the first six months after administration. M. bovis BCG is a fully licensed vaccine that has been in routine clinical use for the last 50 years. It is the most widely administered vaccine in the world today and has an excellent safety record.

Conditions

Interventions

BIOLOGICAL

BCG

Sponsors & Collaborators

  • University of Oxford

    lead OTHER

Principal Investigators

  • Helen I McShane · University of Oxford

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2001-11-30
Completion
2002-05-31

Countries

  • United Kingdom

Study Locations

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Drugs
Diseases

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 NCT00480688 on ClinicalTrials.gov