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OpenTrials
Completed

NCT Number: NCT00786409

Immunogenicity and Safety of HPV Vaccine Gardasil in Young Women

The purpose of this study is to evaluate the immunogenicity and safety of the HPV vaccine Gardasil in young women.

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Key information

Age range

9 year–26 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Chicago

Chicago, Illinois, 60637, United States

About this study

Female patients with systemic lupus erythematosus (SLE) have been found have higher rates of persistent HPV infections and precancerous lesions compared to the healthy population. The HPV vaccine Gardasil has been found to be safe and efficacious in females aged 9 to 26 years. There are no data on the immunogenicity and safety of Gardasil in females with SLE. Immune dysfunction related to SLE itself and the immunosuppression secondary to treatment of SLE might prevent patients with SLE from developing an adequate immune response to the vaccine. Also, theoretically, the vaccine might induce a disease exacerbation or production of new autoantibodies.

The purpose of this study is to evaluate immunogenicity and safety of Gardasil and its effects on autoantibody profile in female SLE patients aged 9-26 years

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 9 to 26 years of age
  • Gender: Female
  • All patients must fulfill the revised American College of Rheumatology Classification Criteria for SLE diagnosis.
  • Current SLEDAI score ≤ 6
  • Written, witnessed informed consent and/or assent will be obtained from the subject and the subject's parents (if under 18 years of age) or legally acceptable representative prior to enrollment

Exclusion criteria

  • Acute exacerbation of disease within past 30 days which required increase in corticosteroid dose, initiation of a new immunosuppressive medication, or hospitalization
  • Current SLEDAI score > 6
  • Patients who have received rituximab in the last 6 months, or are currently on cyclophosphamide treatment
  • History of allergic disease or reactions likely to be exacerbated by any component of the study vaccine
  • Previous administration of any HPV vaccine

Treatment and study plan

GARDASIL

Biological

0.5 ml Gardasil vaccine will be administered to each patient at months 0,2 and 6.

Primary outcomes

  1. Anti-HPV 6 Seroconversion

    Time frame: 7 months

    Percent Seropositive

  2. Anti-HPV 6 GMT

    Time frame: 7 months

    Geometric mean titre in milli-Merck units per ml (mMu/ml)

  3. Anti-HPV 11 Seroconversion

    Time frame: 7 months

    % Seropositive

  4. Anti-HPV 11 GMT

    Time frame: 7 months

    Geometric mean titre in milli-Merck units per ml (mMu/ml)

  5. Anti-HPV 16 Seroconversion

    Time frame: 7 months

    % Seropositive

  6. Anti-HPV 16 GMT

    Time frame: 7 months

    Geometric mean titre in milli-Merck units per ml (mMu/ml)

  7. Anti-HPV 18 Seroconversion

    Time frame: 7 months

    % Seropositive

  8. Anti-HPV 18 GMT

    Time frame: 7 months

    Geometric mean titre in milli-Merck units per ml (mMu/ml)

  9. SLEDAI Change Score

    Time frame: 7 months

    Systemic Lupus Erythematosus Disease Activity Index (SLEDAI): change from baseline to 7 months. The SLEDAI scale is a weighted sum of 16 clinical and 8 laboratory items. Scores range from 0 to 105 with higher scores indicating worse outcome. The variable analyzed here is the 7 month score minus the baseline score. Therefore negative values indicate an improvement in outcome.

Secondary outcomes

  1. Induction or Increase of Autoantibodies (Conversion From Negative Anti-RNP to Positive Anti-RNP) Anti-RNP

    Time frame: 7 months

  2. Induction or Increase of Autoantibodies (Conversion From Negative Smith to Positive Smith)

    Time frame: 7 months

  3. Induction or Increase of Autoantibodies (Conversion From Lupus Anticoagulant Negative to Lupus Anticoagulant Positive)

    Time frame: 7 months

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Collaborators

  • Merck Sharp & Dohme LLC

Registry information

Official study title

Immunogenicity and Safety of the Quadrivalent HPV Vaccine Gardasil in Female Systemic Lupus Erythematosus Patients Aged 9-26

Important dates

Study start
2008
Primary completion
2010
Study completion
2011
First posted
Nov 6, 2008
Registry last updated
Feb 15, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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