Safety and immunogenicity of GSK Biologicals’ HPV-16/18 L1 VLP AS04 vaccine (GSK-580299) in healthy female children 4-6 years old.

• Conditions: Healthy volunteers; Therapeutic area: Diseases [C] - Cancer [C04]

• Registration Number: EUCTR2011-005604-15-Outside-EU/EEA
• Lead Sponsor: GlaxoSmithKline Biologicals

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-10-07
• Last Update Posted: 12 October 2015

Recruitment & Eligibility

• Status: A
• Sex: Female
• Target Recruitment: 148

Inclusion Criteria

•Subjects who the investigator believes that parent(s)/Legally Acceptable Representative(s) [LAR(s)] can and will comply with the requirements of the protocol.
•A female between, and including, 4 and 6 years of age at the time of the first vaccination.
•Written informed consent obtained from the parent(s)/LAR(s) of the subject prior to enrolment in the study.
•Healthy subjects as established by medical history and clinical examination before entering into the study.
•Subjects who received four doses of DTP vaccine (i.e., three doses in the first year of life and a fourth dose in the second year of life) according to the schedule applicable in the participating countries.
•Subjects who received a first dose of MMR vaccine according to the schedule applicable in the participating countries.
Are the trial subjects under 18? yes
Number of subjects for this age range: 148
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Child in care.
•Previous vaccination against HPV or planned administration of another HPV vaccine during the study other than that foreseen in the protocol.
•Planned administration/administration of a vaccine not fore-seen by the study protocol within 30 days before the first dose of study vaccine(s). Administration of routine meningococcal, hepatitis B, hepatitis A, inactivated influenza and/or poliomyelitis vaccines up to 8 days before the first dose of study vaccine(s) is allowed. Enrolment will be deferred until the subject is outside of specified window.
•Use of any investigational or non-registered product (drug or vaccine) other than the study vaccines within 30 days pre-ceding the first dose of study vaccine(s), or planned use during the study period.
•History of any reactions or hypersensitivity likely to be exac-erbated by any component of the study vaccines, including latex and/or obvious allergic reactions to neomycin (a history of contact dermatitis to neomycin is not a contraindication), egg protein, etc. (e.g. hives, swelling of the mouth and throat, difficulty breathing, hypotension, or shock subsequent to egg ingestion).
•Cancer or autoimmune disease under treatment.
•Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product (pharmaceutical product or device).
•Previous administration of MPL or AS04 adjuvant.
•Administration of immunoglobulins and/or any blood products within the three months preceding the first dose of study vaccine(s) or planned administration during the study period.
•Any confirmed or suspected immunosuppressive or immu-nodeficient condition, based on medical history and physical examination (no laboratory testing required).
•Family history of congenital or hereditary immunodeficiency.
•Documented human immunodeficiency virus (HIV)-positive subject.
•Major congenital defects or serious chronic illness.
•History of seizures or serious neurological disorder, which, according to the judgment of the investigator, precludes ad-ministration of any of the study vaccines.
•Acute or chronic, clinically significant pulmonary, cardiovas-cular, hepatic or renal functional abnormality, as determined by physical examination or laboratory screening tests, which in the opinion of the investigator precludes administration of the study vaccine(s).
•Acute disease and/or fever at the time of enrolment.
•Fever is defined as temperature = 37.5°C on oral, axillary or tympanic setting, or = 38.0°C on rectal setting.
•Subjects with a minor illness (such as mild diarrhoea, mild upper respiratory infection) without fever may, be enrolled at the discretion of the investigator. Enrolment can be deferred until condition is resolved.
•Previous administration of the fifth dose of DTP vaccine and/or the second dose of MMR vaccine or planned administration of DTP vaccine and/or MMR vaccine outside the study (during the study period from Day 0 to Month 12).
•History of tetanus, diphtheria, pertussis, measles, mumps and/or rubella.
•Known exposure to diphtheria or household exposure to pertussis within 30 days prior to vaccination with DTPa.
•Known exposure to measles, mumps and/or rubella 30 days prior to vaccination with the MMR study vaccine.
•Confirmed or suspected tuberculosis.
•Severe allergic reactions (e.g. anaphylaxis or severe Arthus-type hypersensitivity rea

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified