Trial record 1 of 1 for:    NCT00128661
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Vaccine To Prevent Cervical Intraepithelial Neoplasia or Cervical Cancer in Younger Healthy Participants

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00128661
First received: August 8, 2005
Last updated: May 24, 2012
Last verified: May 2012

August 8, 2005
May 24, 2012
June 2004
December 2010   (final data collection date for primary outcome measure)
Number of Histopathologically Confirmed Cervical Intraepithelial Neoplasia (CIN)2+ Cases Associated With HPV16 and/or HPV18 Infection Detected in the Preceding Cervical Cytology Specimen. [ Time Frame: From Month 6 up to Month 48 ] [ Designated as safety issue: No ]

CIN2+ was defined as CIN grade 2 (CIN2), CIN grade 3 (CIN3), adenocarcinoma in situ (AIS) or invasive cervical cancer.

Preceding cervical cytology means the last cervical cytology specimen collected before the histopathology specimen was obtained.

Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) by polymerase chain reaction (PCR) at Month 0 and Month 6 for the corresponding HPV-type.

Not Provided
Complete list of historical versions of study NCT00128661 on ClinicalTrials.gov Archive Site
  • Number of Cervical Infection With HPV16 or HPV18. [ Time Frame: From Month 6 up to Month 48 ] [ Designated as safety issue: No ]
    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type
  • Number of Histopathologically Confirmed CIN2+ Cases Associated With Infection by Any Oncogenic HPV Type [ Time Frame: From Month 6 up to Month 48 ] [ Designated as safety issue: No ]

    Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 and 68 detected by polymerase chain reaction (PRC) in the preceding cervical cytology specimen.

    Note: The assay did not distinguish between HPV types 68 and 73.

    CIN2+ was defined as CIN grade 2 (CIN2), CIN grade 3 (CIN3), adenocarcinoma in situ (AIS) or invasive cervical cancer

    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type

  • Number of Persistent Infection (12-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18 Cases [ Time Frame: From Month 6 up to Month 48 ] [ Designated as safety issue: No ]

    Persistent incident HPV-16 and /or HPV-18 cervical infection had to fulfil the following criteria: first detection after the 6-month visit, 2 same type HPV positive (by PCR) test results 10+ months apart, and no intervening HPV negative tests for the corresponding type.

    Persistent HPV16 or HPV18 cervical infection = detection of the same HPV type by polymerase chain reaction (PCR) in cervical samples from all consecutive evaluations over approximately 12 months.

    Subjects were HPV deoxyribonucleic acid (DNA) negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type.

  • Geometric Mean Titers (GMTs) for HPV-16 Antibody in the Immunogenicity Subcohort. [ Time Frame: Before vaccination and at Month 1, 6, 7, 12, 18, 24, 30, 36, 42 and 48 ] [ Designated as safety issue: No ]

    Titers were assessed for the 600 subjects enrolled into the immunogenicity subcohort by Enzyme linked immunosorbent assay (ELISA) and expressed as geometric mean titers (GMTs).

    Seronegative subjects = antibody concentration below 8 ELISA Units per millilitre (EL.U/mL) prior to vaccination.

    Seropositive subjects=antibody concentration equal to or above 8 EL.U/mL prior to vaccination.

    Immunogenicity subcohort = subset of 600 subjects from the 2 groups of the ATP cohort: subjects attended 1 extra clinic visit approximately 1 month (30 to 60 days) after the last dose was administered (Month 7)

  • Geometric Mean Titers (GMTs) for HPV-18 Antibody in the Immunogenicity Subcohort [ Time Frame: Before vaccination and at Month 1, 6, 7, 12, 18, 24, 30, 36, 42 and 48 ] [ Designated as safety issue: No ]

    Titers were assessed for the 600 subjects enrolled into the immunogenicity subcohortby Enzyme linked immunosorbent assay (ELISA) and expressed as geometric mean titers (GMTs).

    Seronegative (Sero-) subjects=antibody concentration below 7 EL.U/mL prior to vaccination.

    Seropositive (Sero+) subjects=antibody concentration equal to or above 7 EL.U/mL prior to vaccination.

    Immunogenicity subcohort=subset of 600 subjects from the 2 groups of the ATP cohort: subjects attended 1 extra clinic visit approximately 1 month (30 to 60 days) after the last dose was administered (Month 7).

  • HPV-16 Geometric Mean Titers (GMTs) (V5 Monoclonal Antibody Inhibition Test) [ Time Frame: Before vaccination and at Month 1, 6, 7, 12, 18, 24, 30, 36, 42 and 48 ] [ Designated as safety issue: No ]

    Titers were assessed for the 600 subjects enrolled into the immunogenicity subcohort by Inhibition Enzyme Immunoassay (EIA) and expressed as geometric mean antibody titers (GMTs).

    Seronegative (Sero-) subjects=antibody concentration below 41 EL.U/mL prior to vaccination.

    Seropositive (Sero+) subjects=antibody concentration equal to or above 41 EL.U/mL prior to vaccination.

    Immunogenicity subcohort=subset of 600 subjects from the 2 groups of the ATP cohort: subjects attended 1 extra clinic visit approximately 1 month (30 to 60 days) after the last dose was administered (Month 7).

  • HPV-18 Geometric Mean Titers (GMTs) (J4 Monoclonal Antibody Inhibition Test) [ Time Frame: Before vaccination and at Month 1, 6, 7, 12, 18, 24, 30, 36, 42 and 48 ] [ Designated as safety issue: No ]

    Titers were assessed for the 600 subjects enrolled into the immunogenicity subcohort by Inhibition Enzyme Immunoassay (EIA) and expressed as geometric mean antibody titers (GMTs).

    Seronegative (Sero-) subjects=antibody concentration below 110 EL.U/mL prior to vaccination.

    Seropositive (Sero+) subjects=antibody concentration equal to or above 110 EL.U/mL prior to vaccination.

    Immunogenicity subcohort=subset of 600 subjects from the 2 groups of the ATP cohort: subjects attended 1 extra clinic visit approximately 1 month (30 to 60 days) after the last dose was administered (Month 7).

  • Number of Subjects Reporting Any and Grade 3 Solicited Local Symptoms. [ Time Frame: Within 60 minutes after vaccination ] [ Designated as safety issue: No ]
    Solicited local symptoms assessed were pain, redness and swelling. Any was defined as any solicited local symptom reported irrespective of intensity. Grade 3 pain was defined as pain that prevented normal everyday activities as assessed by inability to attend work or school and which necessitated the administration of corrective therapy. Grade 3 redness and swelling was defined as redness/swelling above 50 millimeter (mm).
  • Number of Subjects Reporting Any and Grade 3 Solicited General Symptoms. [ Time Frame: Within 60 minutes after vaccination ] [ Designated as safety issue: No ]
    Solicited general symptoms assessed were arthralgia, fatigue, gastrointestinal, headache, myalgia, rash, urticaria and fever (Fever = oral temperature equal to or above (≥) 37.5 degrees Celsius (°C)). Any = any solicited general symptom reported irrespective of intensity and relationship to vaccination. Grade 3 symptoms = symptoms that prevented normal everyday activities as assessed by inability to attend work or school and which necessitated the administration of corrective therapy.Grade 3 urticaria = urticaria distributed on at least 4 body areas. Grade 3 fever = oral temperature > 39.0°C.
  • Number of Subjects Reporting Any and Grade 3 Solicited Local Symptoms on a 10% Random Subset of Participants. [ Time Frame: From Day 3 to Day 6 after vaccination ] [ Designated as safety issue: No ]
    Solicited local symptoms assessed were pain, redness and swelling. Any was defined as any solicited local symptom reported irrespective of intensity. Grade 3 pain was defined as pain that prevented normal everyday activities as assessed by inability to attend work or school and which necessitated the administration of corrective therapy. Grade 3 redness and swelling was defined as redness/swelling above 50 millimeter (mm).
  • Number of Subjects Reporting Any and Grade 3 Solicited General Symptoms on a 10% Random Subset of Participants. [ Time Frame: From Day 3 to Day 6 after vaccination ] [ Designated as safety issue: No ]
    Solicited general symptoms assessed were arthralgia, fatigue, gastrointestinal, headache, myalgia, rash, urticaria and fever (Fever = oral temperature equal to or above (≥) 37.5 degrees Celsius (°C)). Any = any solicited general symptom reported irrespective of intensity and relationship to vaccination. Grade 3 symptoms = symptoms that prevented normal everyday activities as assessed by inability to attend work or school and which necessitated the administration of corrective therapy.Grade 3 urticaria = urticaria distributed on at least 4 body areas. Grade 3 fever = oral temperature > 39.0°C.
  • Number of Subjects Reporting Serious Adverse Events (SAEs). [ Time Frame: During the entire study period (From Month 0 up to Month 48). ] [ Designated as safety issue: No ]
    SAEs assessed include medical occurrences that results in death, are life threatening, require hospitalization or prolongation of hospitalization, results in disability/incapacity or are a congenital anomaly/birth defect in the offspring of a study subjects.
  • Number of Subjects Reporting Unsolicited Adverse Events (AEs). [ Time Frame: During the entire study period (From Month 0 up to Month 48). ] [ Designated as safety issue: No ]
    An unsolicited adverse event is any adverse event (i.e. any untoward medical occurrence in a patient or clinical investigation subject, temporally associated with use of a medicinal product, whether or not considered related to the medicinal product) reported in addition to those solicited during the clinical study and any solicited symptom with onset outside the specified period of follow-up for solicited symptoms.
  • Number of Subjects With All Possible Pregnancy Outcomes [ Time Frame: During the entire study period (From Month 0 up to Month 48). ] [ Designated as safety issue: No ]
    The range of possible pregnancy outcomes was: Pregnancy loss, Pregnancy resolved alive, and Unresolved pregnancy.
  • Number of Cervical Infection With HPV16 or HPV18. [ Time Frame: During the first year of follow-up period ] [ Designated as safety issue: No ]
    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type
  • Number of Cervical Infection With HPV16 or HPV18. [ Time Frame: During the second year of follow-up period ] [ Designated as safety issue: No ]
    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type
  • Number of Cervical Infection With HPV16 or HPV18. [ Time Frame: During the third year of follow-up period ] [ Designated as safety issue: No ]
    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type
  • Number of Cervical Infection With HPV16 or HPV18. [ Time Frame: From the fourth year follow-up period ] [ Designated as safety issue: No ]
    Subjects were human papillomavirus (HPV) deoxyribonucleic acid (DNA) negative (DNA-) (by PCR) at Month 0 and Month 6 for the corresponding HPV-type
  • Number of Subjects Reporting Unsolicited Adverse Events (AEs). [ Time Frame: within 30 days (Days 0-29) after vaccination ] [ Designated as safety issue: No ]
    An unsolicited adverse event is any adverse event (i.e. any untoward medical occurrence in a patient or clinical investigation subject, temporally associated with use of a medicinal product, whether or not considered related to the medicinal product) reported in addition to those solicited during the clinical study and any solicited symptom with onset outside the specified period of follow-up for solicited symptoms.
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Vaccine To Prevent Cervical Intraepithelial Neoplasia or Cervical Cancer in Younger Healthy Participants
A Double-Blind, Controlled, Randomized, Phase III Study of the Efficacy of an HPV16/18 VLP Vaccine in the Prevention of Advanced Cervical Intraepithelial Neoplasia (CIN2, CIN3, Adenocarcinoma In Situ [AIS] and Invasive Cervical Cancer) Associated With HPV 16 or HPV 18 Cervical Infection in Healthy Young Adult Women in Costa Rica.

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer form forming, growing, or coming back. Vaccines may help the body build an effective immune response against human papillomavirus and may be effective in preventing cervical intraepithelial neoplasia or cervical cancer. It is not yet known whether human papillomavirus vaccine is more effective than hepatitis A vaccine in preventing cervical intraepithelial neoplasia or cervical cancer.

PURPOSE: This randomized phase III trial is studying human papillomavirus vaccine to see how well it works compared to hepatitis A vaccine in preventing cervical intraepithelial neoplasia or cervical cancer in younger healthy participants.

OBJECTIVES:

Primary

•Demonstrate the efficacy of the candidate vaccine, human papillomavirus 16/18 (HPV 16/18) L1 virus-like particle (VLP)/AS04 vaccine compared with control in preventing grade 2 or 3 cervical intraepithelial neoplasia, adenocarcinoma in situ of the cervix, or invasive cervical cancer (CIN2+) associated with HPV 16 or HPV 18 cervical infection in younger healthy participants who are negative for HPV DNA by polymerase chain reaction (PCR) for the corresponding HPV type at months 0 and 6.

Secondary

  • Determine the duration of protection against HPV 16 or HPV 18 cervical infection in participants treated with the HPV 16/18 L1 VLP/AS04 vaccine.
  • Determine the safety of this vaccine in these participants, regardless of their initial HPV 16/18 DNA status.
  • Evaluate the efficacy of the candidate vaccine, HPV 16/18 L1 VLP/AS04 vaccine compared with control in preventing CIN2+ associated with any oncogenic HPV type cervical infection in participants who are negative for HPV DNA by PCR for the corresponding HPV type at months 0 and 6.
  • Compare the efficacy of the candidate vaccine with control in preventing CIN2+ associated with HPV 16 or HPV 18 cervical infection, detected within the lesional component of the cervical tissue specimen by PCR, in participants who are negative for HPV DNA by PCR for the corresponding HPV type at months 0 and 6 and by enzyme-linked immunosorbent assay (ELISA) at month 0.
  • Compare the efficacy of the candidate vaccine with control in preventing persistent HPV 16 or HPV 18 cervical infection in these participants.
  • Determine the immunogenicity of HPV 16/18 L1 VLP/AS04 vaccine by ELISA and V5/J4 monoclonal antibody inhibition enzyme immunoassay in the first 600 participants randomized to receive HPV 16/18 L1 VLP/AS04 vaccine.

OUTLINE: This is a randomized, controlled, double-blind, parallel-group study. Participants are randomized to 1 of 2 treatment arms.

  • Arm I: Participants receive human papillomavirus 16/18 L1 virus-like particle/AS04 vaccine intramuscularly (IM) once in months 0, 1, and 6.
  • Arm II: Participants receive hepatitis A vaccine (Havrix®) IM once in months 0, 1, and 6.

After completion of study treatment, participants are followed at 6 months and then at least annually for 3 years.

PROJECTED ACCRUAL: Approximately 7,500 participants will be accrued for this study.

Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
  • Cervical Cancer
  • Precancerous Condition
  • Biological: human papillomavirus 16/18 L1 virus-like particle/AS04 vaccine
    Three doses of Cervarix vaccine administered on a 0, 1, 6-month schedule
  • Biological: hepatitis A inactivated virus vaccine
    Three doses of Havrix vaccine administered on a 0, 1, 6-month schedule
  • Experimental: Cervarix Group
    Subjects received 3 doses of Cervarix vaccine at study Months 0, 1 and 6. All the vaccine doses were administered intramuscularly in the deltoid region of the non-dominant arm.
    Intervention: Biological: human papillomavirus 16/18 L1 virus-like particle/AS04 vaccine
  • Active Comparator: Havrix Group
    Subjects received 3 doses of Havrix vaccine at study Months 0, 1 and 6. All the vaccine doses were administered intramuscularly in the deltoid region of the non-dominant arm.
    Intervention: Biological: hepatitis A inactivated virus vaccine

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
7466
December 2010
December 2010   (final data collection date for primary outcome measure)

DISEASE CHARACTERISTICS:

•Healthy participants

  • Deemed to be in good general health by history and physical examination

    •Resident of Guanacaste Province of Costa Rica and surrounding areas

  • Must remain a resident for ≥ 6 months after the first study vaccination

PATIENT CHARACTERISTICS:

Age

  • 18 to 25

Performance status

•Not specified

Life expectancy

•Not specified

Hematopoietic

•Not specified

Hepatic

  • No history of chronic hepatitis requiring treatment
  • No acute or chronic clinically significant hepatic function abnormality by physical examination or laboratory findings
  • No known history of hepatitis A infection

Renal

  • No history of kidney disease requiring treatment
  • No acute or chronic clinically significant kidney function abnormality by physical examination or laboratory findings

Cardiovascular

  • No acute or chronic clinically significant cardiovascular function abnormality by physical examination or laboratory findings Pulmonary
  • No acute or chronic clinically significant pulmonary function abnormality by physical examination or laboratory findings Immunology
  • No history of allergic disease
  • No history of autoimmune disorder requiring treatment
  • No history of allergic reaction (e.g., difficulty breathing) to any vaccine
  • No suspected allergy or reaction likely to be exacerbated by a component of the study vaccines (e.g., 2-phenoxyethanol or neomycin)
  • No hypersensitivity to latex
  • No diagnosis or suspicion of any immunodeficient condition by medical history or physical examination Other
  • Not pregnant or nursing

    ◦No delivery within the past 3 months

  • Negative pregnancy test
  • Fertile patients must use effective contraception for 30 days before, during, and for 60 days after completion of study treatment
  • Able to speak or understand Spanish
  • Mentally competent
  • Able to undergo pelvic exam (i.e., no heavy bleeding [menstruation or otherwise] or heavy vaginal discharge)
  • No history of cancer requiring treatment
  • No history of diabetes requiring treatment
  • No history of other chronic conditions requiring treatment
  • No acute or chronic clinically significant neurologic function abnormality by physical examination or laboratory findings
  • No other acute disease
  • No fever ≥ 37.5º C

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • More than 6 months since prior chronic administration (i.e., > 14 days) of immune-modulating drugs
  • More than 90 days since prior immunoglobulins
  • More than 30 days since prior and no other concurrent investigational or non-registered vaccines
  • More than 30 days since prior registered vaccines
  • More than 8 days since prior routine meningococcal, hepatitis B, influenza, or diphtheria/tetanus vaccine
  • No prior vaccination against hepatitis A
  • No prior vaccination against human papillomavirus
  • No prior monophosphoryl lipid A or AS04 adjuvant

Chemotherapy

•Not specified

Endocrine therapy

  • More than 6 months since prior chronic administration (i.e., > 14 days) of corticosteroids (e.g., ≥ 0.5 mg/kg/day of prednisone or equivalent)
  • Concurrent inhaled or topical steroids allowed

Radiotherapy

•Not specified

Surgery

•No prior hysterectomy

Other

  • More than 6 months since prior chronic administration (i.e., > 14 days) of immunosuppressants
  • More than 30 days since prior and no other concurrent investigational or non-registered drugs
Female
18 Years to 25 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Costa Rica
 
NCT00128661
CDR0000441189, NCI-04-C-N191, NCI-590299/009, GSK-590299/009
Not Provided
GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
May 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP