A phase IIIb, randomized, open, multicentre study to evaluate the immunogenicity and safety of GlaxoSmithKline Biologicals’ HPV-16/18 L1 VLP AS04 vaccine co-administered with GlaxoSmithKline Biologicals’ inactivated hepatitis A and hepatitis B vaccine adsorbed (Twinrix® Paediatric) in healthy female subjects aged 9–15 years. - HPV-029 PRI

GlaxoSmithKline Biologicals0 sites814 target enrollmentOctober 17, 2007

ConditionsFor active immunization of females from the age of 10 years onwards for the prevention of cervical cancer by protecting against incident and persistent infections, cytological abnormalities including atypical squamous cells of undetermined significance (ASC-US), cervical intraepithelial neoplasia (CIN) and pre-cancerous lesions (CIN 2/3) caused by oncogenic human papillomavirus (HPV) types 16 and 18.

DrugsCervarix Twinrix Paediatric

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: For active immunization of females from the age of 10 years onwards for the prevention of cervical cancer by protecting against incident and persistent infections, cytological abnormalities including atypical squamous cells of undetermined significance (ASC-US), cervical intraepithelial neoplasia (CIN) and pre-cancerous lesions (CIN 2/3) caused by oncogenic human papillomavirus (HPV) types 16 and 18.
Sponsor: GlaxoSmithKline Biologicals
Enrollment: 814
Status: Active, not recruiting
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

October 17, 2007

End Date

April 28, 2009

Last Updated

4 years ago

Study Type

Interventional clinical trial of medicinal product

Sex

Female

Investigators

Sponsor

GlaxoSmithKline Biologicals

Eligibility Criteria

Inclusion Criteria

•All subjects must satisfy the following criteria at study entry:
•Subjects who the investigator believes that they and/or their legally acceptable representatives (LARs) can and will comply with the requirements of the protocol should be enrolled in the study.
•A female between, and including, 9 and 15 years of age at the time of the first vaccination.
•Written informed consent obtained from subject's LAR and written informed assent obtained from the subject.
•Healthy subjects as established by medical history and clinical examination before entering into the study.
•Subjects must not be pregnant. Absence of pregnancy should be verified with a urine pregnancy test.
•Subjects must be of non\-childbearing potential, i.e., have a current tubal ligation, hysterectomy, ovariectomy or be pre\-menarcheal, or if the subject is of childbearing potential, she must be abstinent or use adequate contraception for 30 days prior to vaccination and must agree to continue such precautions for two months after completion of the vaccination series. Subjects who reach menarche (begin menstruating) during the study, and therefore become of childbearing potential, must agree to follow the same precautions.
•Are the trial subjects under 18? yes
•Number of subjects for this age range:
•F.1\.2 Adults (18\-64 years) no

Exclusion Criteria

•The following criteria should be checked at the time of study entry. If any apply, the subject must not be included in the study:
•Use of any investigational or non\-registered product (drug or vaccine) other than the study vaccines within 30 days preceding the first dose of study vaccine, or planned use during the study period.
•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).
•Chronic administration (defined as more than 14 consecutive days) of immunosuppressants or other immune\-modifying drugs within six months prior to the first vaccine dose.
•Planned administration/administration of a vaccine not foreseen by the study protocol within 30 days before and 30 days after each dose of vaccine(s).
•A subject planning to become pregnant, likely to become pregnant (as determined by the investigator) or planning to discontinue contraceptive precautions during the study period and up to two months after the last vaccine dose.
•Pregnant or breastfeeding women.
•Previous vaccination against HPV or planned administration of any HPV vaccine other than that foreseen by the study protocol during the study period.
•Previous administration of MPL or AS04 adjuvant.
•Previous vaccination against hepatitis A or B or planned administration of any hepatitis A or B vaccine other than that foreseen by the study protocol during the study period.