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Immunogenicity and Safety Study of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus Vaccine (Cervarix™) When Co-administered With GSK Biologicals' Hepatitis A Vaccine (Havrix®) in Healthy Female Adolescents Aged 9-14 Years

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ClinicalTrials.gov Identifier: NCT02082639
Recruitment Status : Withdrawn (Because the Russian Authorities already approved the 2-dose Cervarix™ schedule, the study was no longer needed for registration and hence it was cancelled.)
First Posted : March 10, 2014
Last Update Posted : July 20, 2015
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline

Brief Summary:
The purpose of this study is to evaluate the immunogenicity and safety of two doses of GSK Biologicals' HPV-16/18 L1 VLP AS04 vaccine when co-administered with GSK Biologicals' HAV vaccine according to 0, 6 month schedule, compared to the administration of either of these vaccines alone. The study will ascertain that the immune responses elicited to the two vaccines are not adversely impacted compared to when HPV-16/18 L1 VLP AS04 vaccine and HAV vaccine are administered alone.

Condition or disease Intervention/treatment Phase
Infections, Papillomavirus Biological: Cervarix™ Biological: Havrix Phase 3

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Immunogenicity and Safety Study of GSK Biologicals' Human Papillomavirus (HPV) Vaccine (Cervarix™) (GSK-580299) When Co-administered With GSK Biologicals' Hepatitis A Vaccine (Havrix®) (GSK-208109) in Healthy Female Adolescents Aged 9-14 Years
Study Start Date : February 2015
Estimated Primary Completion Date : August 2015
Estimated Study Completion Date : November 2015

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: HPV Group
Subjects will receive two doses of HPV vaccine intramuscularly
Biological: Cervarix™
2 doses intramuscularly in the deltoid muscle of the non-dominant arm

Experimental: HAV Group
Subjects will receive two doses of HAV vaccine intramuscularly
Biological: Havrix
2 doses intramuscularly in the deltoid muscle of the dominant arm

Experimental: HPV+HAV Group
Subjects will receive two doses of both HPV and HAV vaccines intramuscularly
Biological: Cervarix™
2 doses intramuscularly in the deltoid muscle of the non-dominant arm

Biological: Havrix
2 doses intramuscularly in the deltoid muscle of the dominant arm




Primary Outcome Measures :
  1. Anti-HPV-16/18 seroconversion status in the HPV group and the HPV+HAV group [ Time Frame: One month after the second dose (Month 7) ]
  2. Anti-HPV-16/18 antibody titres in the HPV group and the HPV+HAV group [ Time Frame: One month after the second dose (Month 7) ]
  3. Anti-HAV seroconversion status in the HPV+HAV group and the HAV group [ Time Frame: One month after the second dose (Month 7) ]
  4. Anti-HAV antibody titres in the HPV+HAV group and the HAV group [ Time Frame: One month after the second dose (Month 7) ]

Secondary Outcome Measures :
  1. Anti-HPV-16/18 seroconversion status in the HPV group and the HPV+HAV group [ Time Frame: One month after the second dose (Month 7) ]
  2. Anti-HPV-16/18 antibody titres in the HPV group and the HPV+HAV group [ Time Frame: One month after the second dose (Month 7) ]
  3. Anti-HAV seroconversion status in the HPV+HAV group and the HAV group [ Time Frame: One month after the second dose (Month 7) ]
  4. Anti-HAV antibody titres in the HPV+HAV group and the HAV group [ Time Frame: One month after the second dose (Month 7) ]
  5. Occurrence of any and Grade 3 solicited local symptoms (injection site pain, redness and swelling) in all study groups [ Time Frame: During the 7-day period (Day 0-6) following each vaccination ]
  6. Occurrence of any, Grade 3 and causally related to vaccination solicited general symptoms in all study groups [ Time Frame: During the 7-day period (Day 0-6) following each vaccination ]
  7. Occurrence of any, Grade 3 and causally related to vaccination unsolicited AEs in all study groups [ Time Frame: During the 30-day period (Day 0-29) following any vaccination ]
  8. Occurrence of any and causally related to vaccination serious adverse events (SAEs) in all groups [ Time Frame: Throughout the active phase of the study (up to Month 7) and during the extended safety follow-up period (up to Month 12) ]
  9. Occurrence of medically significant conditions (MSCs) in all groups [ Time Frame: Throughout the active phase (up to Month 7) and during the extended safety follow-up period (up to Month 12) ]
  10. Occurrence of potential immune-mediated diseases (pIMDs) in all groups [ Time Frame: Throughout the active phase (up to Month 7) and during the extended safety follow-up period (up to Month 12) ]
  11. Occurrence of pregnancies and pregnancy outcomes [ Time Frame: During the entire study period (Month 0 - Month 12) ]


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Ages Eligible for Study:   9 Years to 14 Years   (Child)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • A female between, and including, 9 and 14 years of age at the time of the first vaccination.
  • Subjects' parent(s)/Legally Acceptable Representative(s) [LAR(s)] who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
  • Written informed consent obtained from the parent(s)/LAR(s) of the subject and informed assent obtained from the subject, if appropriate, prior to enrollment.
  • Healthy subjects as established by medical history and clinical examination before entering into the study.
  • Female subjects of non-childbearing potential may be enrolled in the study.
  • Female subjects of childbearing potential may be enrolled in the study, if the subject:

    • has practiced adequate contraception for 30 days prior to vaccination, and
    • has a negative pregnancy test on the day of vaccination, and
    • has agreed to continue adequate contraception during the entire treatment period and for two months after completion of the vaccination series.

Exclusion Criteria:

  • Child in care.
  • Use of any investigational or non-registered product other than the study vaccine within 30 days preceding the first dose of study vaccine, or planned use during the study period (up to Month 12).
  • Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose. Inhaled and topical steroids are allowed.
  • Planned administration/administration of a vaccine not foreseen by the study protocol within the period starting 30 days before and 30 days after the first dose of vaccine with the exception of routine vaccines such as meningococcal, pertussis, inactivated influenza, diphtheria/tetanus and/or diphtheria/tetanus-containing vaccines up to 8 days before the first dose of study vaccine.
  • Concurrently participating in another clinical study, at any time during the study period (up to Month 12), in which the subject has been or will be exposed to an investigational or a non-investigational vaccine/product.
  • Previous vaccination against HPV or planned administration of any HPV vaccine other than that foreseen by the study protocol during the study period (up to Month 12).
  • Previous administration of MPL or AS04 adjuvant.
  • Previous vaccination against hepatitis A or planned administration of any hepatitis A vaccine other than that foreseen by the study protocol during the study period (up to Month 12).
  • Cancer or autoimmune disease under treatment.
  • History of hepatitis A infection.
  • Known exposure to hepatitis A within the previous 6 weeks.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination.
  • History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccines.
  • Hypersensitivity to latex.
  • Acute or chronic, clinically significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by physical examination or laboratory screening tests, which in the opinion of the investigator preclude administration of the study vaccine.
  • Administration of immunoglobulins and/or any blood products within the 3 months preceding the first dose of study vaccine or planned administration during the study period (up to Month 12).
  • Acute disease and/or fever at the time of enrollment.

    • Fever is defined as temperature ≥ 37.0°C for oral, axillary or tympanic route. The preferred route for recording temperature in this study will be oral or axillary.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02082639


Sponsors and Collaborators
GlaxoSmithKline
Investigators
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Study Director: GSK Clinical Trials GlaxoSmithKline
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Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT02082639    
Other Study ID Numbers: 117099
2012-004378-24 ( EudraCT Number )
First Posted: March 10, 2014    Key Record Dates
Last Update Posted: July 20, 2015
Last Verified: July 2015
Keywords provided by GlaxoSmithKline:
Adolescents
Havrix
Immunogenicity
Cervarix
Safety
Additional relevant MeSH terms:
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Hepatitis A
Hepatitis
Liver Diseases
Digestive System Diseases
Hepatitis, Viral, Human
Virus Diseases
Infections
Enterovirus Infections
Picornaviridae Infections
RNA Virus Infections