Expired Study
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Birmingham, Alabama


Purpose:

This study is a continued evaluation of the immune response to StaphVAX , a Staphylococcus aureus type 5 and 8 capsular polysaccharide conjugate vaccine, in end-stage renal disease patients, by giving a 3rd and 4th dose to a subset of the participants in the previous efficacy trial. Participants continue to receive the vaccine or placebo in a blinded manner, and are also randomly assigned to 1 of 2 different intervals between the doses. The immunogenicity is measured by the antibodies in the blood, and typical vaccine safety information is also collected.


Criteria:

Inclusion Criteria: - Participation in prior study Nabi-1371 - Written informed consent - Negative serum pregnancy test, where appropriate - Expect to comply with protocol procedures and schedule Exclusion Criteria: - Known HIV - Immunomodulatory drugs - Malignancy (other than basal cell or squamous cell carcinoma, carcinoma in situ of the cervix, or early stage prostate cancer) - Active infection in the 2 weeks prior to study injection - Serious S. aureus infection within the last 2 months prior to injection - Hypersensitivity to components of StaphVAX


NCT ID:

NCT00130260


Primary Contact:

Study Director
Matt Hohenboken, MD, PhD
Nabi Biopharmaceuticals


Backup Contact:

N/A


Location Contact:

Birmingham, Alabama
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 10, 2017

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