Study to Evaluate the Efficacy of the Human Papillomavirus Vaccine in Healthy Adult Women of 26 Years of Age and Older
27 grudnia 2019 zaktualizowane przez: GlaxoSmithKline
A Study to Evaluate Safety, Immunogenicity and Efficacy of GSK Biologicals HPV-16/18 L1/AS04 Vaccine Administered Intramuscularly According to a Three-dose Schedule (0, 1, 6 Month) in Healthy Adult Female Subjects Aged 26 Years and Above
This is a multicentre study in which women were planned to receive either the Human Papillomavirus Vaccine (HPV) vaccine or control.
Under Protocol Amendment 3, study participation will last approximately 48 months and involves a total of eleven scheduled visits.
Under Protocol Amendment 4, study participation will last up to 84 months and involves a maximum of seventeen scheduled visits.
Przegląd badań
Status
Zakończony
Interwencja / Leczenie
Szczegółowy opis
The Protocol Posting has been updated due to protocol amendment 5 and in order to comply with the FDA Amendment Act, Sep 2007.
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
5752
Faza
- Faza 3
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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Victoria
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Parkville, Victoria, Australia, 3052
- GSK Investigational Site
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Western Australia
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Perth, Western Australia, Australia
- GSK Investigational Site
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Ekaterinburg, Federacja Rosyjska, 620073
- GSK Investigational Site
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Moscow, Federacja Rosyjska, 117997
- GSK Investigational Site
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Moscow, Federacja Rosyjska, 115 478
- GSK Investigational Site
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Moscow, Federacja Rosyjska, 109263
- GSK Investigational Site
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Sankt-Petersburg, Federacja Rosyjska, 190020
- GSK Investigational Site
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Sankt-Petersburg, Federacja Rosyjska, 199034
- GSK Investigational Site
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Laguna, Filipiny
- GSK Investigational Site
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San Pablo City, Filipiny
- GSK Investigational Site
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Taft Avenue, Manila, Filipiny, 1700
- GSK Investigational Site
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Amsterdam, Holandia, 1007 MB
- GSK Investigational Site
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Delft, Holandia, 2625 AD
- GSK Investigational Site
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Rotterdam, Holandia, 3015 CE
- GSK Investigational Site
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Quebec, Kanada, G1S 2L6
- GSK Investigational Site
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Alberta
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Edmonton, Alberta, Kanada, T6G 2C8
- GSK Investigational Site
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British Columbia
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Vancouver, British Columbia, Kanada, V6H 3N1
- GSK Investigational Site
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3H 2Y9
- GSK Investigational Site
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Truro, Nova Scotia, Kanada, B2N 1L2
- GSK Investigational Site
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Ontario
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Waterloo, Ontario, Kanada, N2L 6H6
- GSK Investigational Site
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Quebec
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Sherbrooke, Quebec, Kanada, J1H 1Z1
- GSK Investigational Site
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Jojutla / Morelos, Meksyk
- GSK Investigational Site
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Morelos
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Cuenavaca, Morelos, Meksyk, 62430
- GSK Investigational Site
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Lima, Peru
- GSK Investigational Site
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Almada, Portugalia, 2805-267 Almada
- GSK Investigational Site
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Coimbra, Portugalia, 3000-075 Coimbra
- GSK Investigational Site
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Lisboa, Portugalia, 1200-831 Lisboa
- GSK Investigational Site
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Porto, Portugalia, 4200-023 Porto
- GSK Investigational Site
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Setúbal, Portugalia, 2910-446 Setúbal
- GSK Investigational Site
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Singapore, Singapur, 119074
- GSK Investigational Site
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Singapore, Singapur, 229899
- GSK Investigational Site
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California
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Fountain Valley, California, Stany Zjednoczone, 92708
- GSK Investigational Site
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Colorado
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Aurora, Colorado, Stany Zjednoczone, 80045
- GSK Investigational Site
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Golden, Colorado, Stany Zjednoczone, 80401
- GSK Investigational Site
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Florida
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Coral Gables, Florida, Stany Zjednoczone, 33134
- GSK Investigational Site
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Miami, Florida, Stany Zjednoczone, 33136
- GSK Investigational Site
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Georgia
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Augusta, Georgia, Stany Zjednoczone, 30912
- GSK Investigational Site
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Iowa
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Iowa City, Iowa, Stany Zjednoczone, 52242
- GSK Investigational Site
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Kansas
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Wichita, Kansas, Stany Zjednoczone, 67207
- GSK Investigational Site
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Kentucky
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Bardstown, Kentucky, Stany Zjednoczone, 40004
- GSK Investigational Site
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Louisville, Kentucky, Stany Zjednoczone, 40202
- GSK Investigational Site
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Minnesota
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Chaska, Minnesota, Stany Zjednoczone, 55318
- GSK Investigational Site
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Nebraska
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Omaha, Nebraska, Stany Zjednoczone, 68131
- GSK Investigational Site
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New Hampshire
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Lebanon, New Hampshire, Stany Zjednoczone, 03756
- GSK Investigational Site
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New Mexico
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Albuquerque, New Mexico, Stany Zjednoczone, 87131
- GSK Investigational Site
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New York
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Syracuse, New York, Stany Zjednoczone, 13057
- GSK Investigational Site
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North Carolina
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Chapel Hill, North Carolina, Stany Zjednoczone, 27514
- GSK Investigational Site
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New Bern, North Carolina, Stany Zjednoczone, 28562
- GSK Investigational Site
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Ohio
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Akron, Ohio, Stany Zjednoczone, 44311
- GSK Investigational Site
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Cleveland, Ohio, Stany Zjednoczone, 44122
- GSK Investigational Site
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Oklahoma
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Tulsa, Oklahoma, Stany Zjednoczone, 74105
- GSK Investigational Site
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Oregon
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Portland, Oregon, Stany Zjednoczone, 97210
- GSK Investigational Site
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Pennsylvania
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Carnegie, Pennsylvania, Stany Zjednoczone, 15106
- GSK Investigational Site
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Erie, Pennsylvania, Stany Zjednoczone, 16508
- GSK Investigational Site
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Erie, Pennsylvania, Stany Zjednoczone, 16507
- GSK Investigational Site
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Philadelphia, Pennsylvania, Stany Zjednoczone, 19107
- GSK Investigational Site
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Pittsburgh, Pennsylvania, Stany Zjednoczone, 15236
- GSK Investigational Site
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Pittsburgh, Pennsylvania, Stany Zjednoczone, 15213
- GSK Investigational Site
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Wexford, Pennsylvania, Stany Zjednoczone, 15090
- GSK Investigational Site
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Texas
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Austin, Texas, Stany Zjednoczone, 78705
- GSK Investigational Site
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Houston, Texas, Stany Zjednoczone, 77030
- GSK Investigational Site
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Houston, Texas, Stany Zjednoczone, 77004
- GSK Investigational Site
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Utah
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Salt Lake City, Utah, Stany Zjednoczone, 84109
- GSK Investigational Site
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Salt Lake City, Utah, Stany Zjednoczone, 84121
- GSK Investigational Site
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South Jordan, Utah, Stany Zjednoczone, 84095
- GSK Investigational Site
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Washington
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Wenatchee, Washington, Stany Zjednoczone, 98801
- GSK Investigational Site
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Wisconsin
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La Crosse, Wisconsin, Stany Zjednoczone, 54601
- GSK Investigational Site
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Bangkok, Tajlandia, 10400
- GSK Investigational Site
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Bangkok, Tajlandia, 10700
- GSK Investigational Site
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Aberdeen, Zjednoczone Królestwo, AB25 7ZD
- GSK Investigational Site
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Cardiff, Zjednoczone Królestwo, CF14 4XN
- GSK Investigational Site
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Gateshead, Zjednoczone Królestwo, NE9 6SX
- GSK Investigational Site
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London, Zjednoczone Królestwo, EC1M 6BQ
- GSK Investigational Site
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Manchester, Zjednoczone Królestwo, M13 9WL
- GSK Investigational Site
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Middlesex
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Northwood, Middlesex, Zjednoczone Królestwo, HA6 2RN
- GSK Investigational Site
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
26 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Tak
Płeć kwalifikująca się do nauki
Kobieta
Opis
Inclusion criteria:
- A woman who the investigator believes that she can and will comply with the requirements of the protocol.
- A women of at least 26 years of age at the time of the first vaccination.
- Written informed consent obtained from the subject prior to enrolment.
- Free of obvious health problems as established by medical history and clinical examination before entering into the study.
- Subject must have intact cervix.
- Subject must have a negative urine pregnancy test. This test is not applicable to women of non-childbearing potential.
- Subject must be of non-childbearing potential or, if of childbearing potential, she must be abstinent or must be using an effective method of birth control for 30 days prior to the first vaccination and must agree to continue such precautions for two months after completion of the vaccination series.
Exclusion criteria:
- Pregnant or breastfeeding (women must be at least three months post-pregnancy and not breastfeeding to enter the study).
- A women planning to become pregnant, likely to become pregnant (as determined by the investigator) or planning to discontinue contraceptive precautions during the vaccination phase of the study, i.e. up to two months after the last vaccine dose (Month 0 - 8).
- Use of any investigational or non-registered product (drug or vaccine) 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 84).
- Chronic administration 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 (i.e. days 0 - 29) the first dose of study vaccine. Planned administration/administration of routine vaccines up to 8 days before the first dose of study vaccine is allowed. Enrolment will be deferred until the subject is outside of specified window.
- Previous administration of components of the investigational vaccine
- Previous vaccination against HPV or planned administration of any HPV vaccine other than that foreseen by the study protocol during the study period.
- History of HPV infection/treatment or planned treatment to evaluate an abnormal cervical cytology (Pap smear) test, e.g. colposcopy.
- Any medically diagnosed or suspected immunodeficient condition based on medical history and physical examination.
- History of allergic disease, suspected allergy or reactions likely to be exacerbated by any component of the study vaccine.
- Hypersensitivity to latex.
- Known acute or chronic, clinically significant neurologic, hepatic or renal functional abnormality, as determined by previous physical examination or laboratory tests.
- History of chronic condition(s) requiring treatment.
- Administration of immunoglobulins and/or any blood product within three months preceding the first dose of study vaccine, or planned administration during the study period. Enrolment will be deferred until the subject is outside of specified window.
- Acute disease at the time of enrolment.
- Heavy bleeding (menstruation or other) or heavy vaginal discharge in which a pelvic exam cannot be performed (and no cervical sample can be taken). Enrolment will be deferred until condition is resolved according to investigators medical judgement.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Zapobieganie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Cervarix Group
Subjects received 3 doses of Cervarix™ vaccine.
Cervarix vaccine was administered intramuscularly into the deltoid region of the non-dominant arm according to a 0, 1, 6 months schedule.
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Subjects were planned to receive three doses of the study vaccine administered intramuscularly according to a 0, 1, 6 month vaccination schedule.
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Komparator placebo: Aluminium Hydroxide Group
Subjects received 3 doses of Aluminium Hydroxide [Al(OH)3].
Aluminium Hydroxide was administered intramuscularly into the deltoid region of the non-dominant arm according to a 0, 1, 6 months schedule.
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Subjects were planned to receive three doses of the control vaccine administered intramuscularly according to a 0, 1, 6 month vaccination schedule.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18 and/or With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection.
Ramy czasowe: Up to Month 48
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CIN1+ = CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Persistent HPV infection = detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
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Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With HPV-16 or HPV-18 and/or With Histopathologically-CIN1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Using the HPV Type Assignment Algorithm (TAA).
Ramy czasowe: Up to Month 48
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CIN1+ = CIN grades 1, 2 and 3, AIS and invasive cervical cancer. Persistent cervical HPV infection (6-month definition) = detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
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Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18 and/or With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection.
Ramy czasowe: Up to Month 84
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CIN1+ = CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer.
Persistent HPV infection = detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
- DNA- and sero-/+: subjects HPV deoxyribonucleic acid (DNA) negative (DNA-) at Month 0 and 6 and seronegative/positive (sero-/+) at Month 0 for the corresponding HPV-type by Enzyme-linked Immunosorbent Assay (ELISA) - Overall: subjects DNA- at Month 0 and 6 for the corresponding HPV-type, regardless of initial serostatus
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Up to Month 84
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Number of Subjects With Persistent Infection (6-month Definition) With HPV-16 or HPV-18 and/or With Histopathologically-CIN1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Using the HPV Type Assignment Algorithm (TAA).
Ramy czasowe: Up to Month 84
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CIN1+ = CIN grades 1, 2 and 3, AIS and invasive cervical cancer.
Persistent cervical HPV infection (6-month definition) = detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
- DNA- and sero-/+: subjects HPV DNA negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative/positive (sero-/+) for HPV-16 and/or HPV-18 by ELISA at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
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Up to Month 84
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18
Ramy czasowe: Up to Month 48
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval. Detection was done in:
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Up to Month 48
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Number of Subjects With Persistent Infection (12-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18
Ramy czasowe: Up to Month 48
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Persistent cervical HPV infection (12-month definition) was defined as the detection of the same HPV type(s) PCR in cervical samples at all available time points over approximately a 12-month interval (evaluations are planned at approximately 6-month intervals).
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Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With Oncogenic HPV Types Individually or in Combinations.
Ramy czasowe: Up to Month 48
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Persistent cervical HPV infection (6-month definition) = detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval. Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. Detection was done in subjects HPV DNA- for the corresponding HPV type at baseline (at month 0 and Month 6) regardless of initial serostatus. HPV-HRW=All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18. HPV-HR=High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. |
Up to Month 48
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Number of Subjects With Persistent Infection (12-month Definition) With Oncogenic HPV Types Individually or in Combinations.
Ramy czasowe: Up to Month 48
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Persistent HPV infection (12-month definition) = detection of the same HPV type(s) by PCR in cervical samples at available time points over approximately a 12-month interval (evaluations are planned at approximately 6-month intervals). Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. subjects HPV DNA- for the corresponding HPV type at Month 0 6, regardless of initial serostatus. HPV-HRW=All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18 HPV-HR=High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 , 68 |
Up to Month 48
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)2+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 48
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CIN2+ was defined as CIN grades 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done in:
Note: Results for seropositive status were not analysed. |
Up to Month 48
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 48
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done in:
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Up to Month 48
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 48
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done on all subjects irrespective of their baseline HPV DNA and serostatus. |
Up to Month 48
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Irrespective of HPV Cervical Infection and Irrespective of Baseline HPV DNA Status
Ramy czasowe: Up to Month 48
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done on all subjects irrespective of their baseline HPV DNA status. |
Up to Month 48
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Number of Subjects With Any Cytological Abnormalities Associated With HPV-16 or HPV-18 Cervical Infection
Ramy czasowe: Up to Month 48
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Cytological abnormalities = atypical squamous cells of undetermined significance (ASC-US). Detection was done in:
Results for seropositive status were not analysed. |
Up to Month 48
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Number of Subjects With Cytological Abnormalities Associated With Oncogenic HPV Types Individually or in Combinations
Ramy czasowe: Up to Month 48
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Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68. Detection was done in subjects who were HPV DNA negative for the corresponding HPV type at baseline (at month 0 and Month 6) regardless of initial serostatus. HRW-HPV= All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18 HPV-HR= High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68 |
Up to Month 48
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Number of Subjects With Histopathologically Confirmed Reduction of Local Cervical Therapy
Ramy czasowe: Up to Month 48
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Detection was done on all subjects irrespective of their baseline HPV DNA status.
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Up to Month 48
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Number of Subjects With First Colposcopy
Ramy czasowe: Up to Month 48
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Detection was done on all subjects irrespective of their baseline HPV DNA status.
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Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18 and/or With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection
Ramy czasowe: Up to Month 48
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval. CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done on all subjects irrespective of their baseline HPV DNA and serostatus. |
Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With HPV-16 or HPV-18 and/or With Histopathologically-confirmed CIN1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Using the HPV Type Assignment Algorithm (TAA).
Ramy czasowe: Up to Month 48
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval. Detection was done on all subjects irrespective of their baseline HPV DNA and serostatus. The lesion was assigned to an HPV type found in the lesion if (1) the same HPV type was found in at least 1 of the 2 (closest) preceding cytology samples, or (2) none of the HPV types found in the lesion were found in any of the 2 preceding cytology samples (isolate HPV types) |
Up to Month 48
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Number of Seroconverted Subjects Against HPV-16 in the Immunogenicity Subset.
Ramy czasowe: At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Seroconversion was defined as the appearance of antibodies (i.e.; titre greater than or equal to the cut-off value) in the serum of subjects seronegative before vaccination. HPV-16 assay cut-off value was defined as greater than or equal to 8 ELISA units per millilitre (EL.U/mL). Seronegative (Sero-) subjects are subjects who had an antibody concentration below 8 EL.U/mL prior to vaccination. Seropositive (Sero+) subjects are subjects who had an antibody concentration equal to or above 8 EL.U/mL prior to vaccination. Immuno subset=subjects from selected sites N≥1000, at least 250 per region |
At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Number of Seroconverted Subjects Against HPV-18 in the Immunogenicity Subset.
Ramy czasowe: At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Seroconversion was defined as the appearance of antibodies (i.e.; titre greater than or equal to the cut-off value) in the serum of subjects seronegative before vaccination. HPV-18 assay cut-off value was defined as greater than or equal to 7 ELISA units per millilitre (EL.U/mL). Seronegative (Sero-) subjects are subjects who had an antibody concentration below 7 EL.U/mL prior to vaccination. Seropositive (Sero+) subjects are subjects who had an antibody concentration equal to or above 7 EL.U/mL prior to vaccination. Immuno subset=subjects from selected sites N≥1000, at least 250 per region |
At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Geometric Mean Concentrations (GMCs) Against HPV-16 Antibody in the Immunogenicity Subset.
Ramy czasowe: At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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GMCs were expressed in ELISA units per milliliter (EL.U/mL). Seronegative (Sero-) subjects are subjects who had an antibody concentration below 8 EL.U/mL prior to vaccination. Seropositive (Sero+) subjects are subjects who had an antibody concentration equal to or above 8 EL.U/mL prior to vaccination. Immuno subset=subjects from selected sites (N≥1000, at least 250 per region) |
At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Geometric Mean Concentrations (GMCs) Against HPV-18 Antibody in the Immunogenicity Subset.
Ramy czasowe: At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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GMCs were expressed in ELISA units per milliliter (EL.U/mL). Seronegative (Sero-) subjects are subjects who had an antibody concentration below 7 EL.U/mL prior to vaccination. Seropositive (Sero+) subjects are subjects who had an antibody concentration equal to or above 7 EL.U/mL prior to vaccination. Immuno subset=subjects from selected sites (N≥1000, at least 250 per region) |
At pre-vaccination and at Month 7, 12, 18, 24, 36, 48, 60, 72 and 84
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Number of Seroconverted Subjects Against HPV-16 and HPV-18 Viral Neutralization in a Selected Subset of Subjects.
Ramy czasowe: Prior to vaccination and at Months 7, 12, 18, 24, 48 and 84.
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Seroconversion was defined as the appearance of antibodies (i.e.; titre greater than or equal to the cut-off value) in the serum of subjects seronegative before vaccination.
HPV-16/18 assay cut-off value was defined as greater than or equal to 40 Estimated dose 50% (ED50).
Sero- subjects are subjects who had an antibody concentration below 40 ED50 prior to vaccination.
Sero+ subjects are subjects who had an antibody concentration equal to or above 50 ED50 prior to vaccination.
ED50 = the estimated serum dilution reducing the signal generated by viral infection by 50%
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Prior to vaccination and at Months 7, 12, 18, 24, 48 and 84.
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Geometric Mean Titers (GMTs) Against HPV-16 and HPV-18 Viral Neutralization Antibodies in a Selected Subset of Subjects.
Ramy czasowe: Prior to vaccination and at Months 7, 12, 18, 24, 48 and 84.
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Titers are expressed as geometric mean antibody titers (GMTs). Seronegative (Sero-) subjects are subjects who had an antibody titer below 40 ED50 prior to vaccination. Seropositive (Sero+) subjects are subjects who had an antibody titer equal to or above 40 ED50 prior to vaccination. ED50 = Estimated dose 50%, the estimated serum dilution reducing the signal generated by viral infection by 50% |
Prior to vaccination and at Months 7, 12, 18, 24, 48 and 84.
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Number of Subjects Reporting Any and Grade 3 Solicited Local Symptoms.
Ramy czasowe: Within 7 days (Days 0-6) after vaccination
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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 activity.
Grade 3 redness and swelling was defined as redness/swelling above 50 millimeter (mm).
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Within 7 days (Days 0-6) after vaccination
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Number of Subjects Reporting Any, Grade 3 and Related Solicited General Symptoms.
Ramy czasowe: Within 7 days (Days 0-6) after vaccination
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Solicited general symptoms assessed were arthralgia, fatigue, gastrointestinal, headache, myalgia, rash, urticaria and fever (Fever = axillary temperature above 37.5 degrees Celsius (°C)).
Any = any solicited general symptom reported irrespective of intensity and relationship to vaccination.
Related = symptoms considered by the investigator to have a causal relationship to vaccination.
Grade 3 symptoms = symptoms that prevented normal activity.
Grade 3 urticaria = urticaria distributed on at least 4 body areas.
Grade 3 fever = axillary temperature above 39.0°C.
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Within 7 days (Days 0-6) after vaccination
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Number of Subjects Reporting Any, Grade 3 and Related Unsolicited Adverse Events (AEs).
Ramy czasowe: Within 30 days (Days 0 - 29) post-vaccination period.
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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. Grade 3 unsolicited AE = an event that prevented normal activity. A related AE = event assessed by the investigator as causally related to the study vaccination. |
Within 30 days (Days 0 - 29) post-vaccination period.
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Number of Subjects Reporting Any and Related Serious Adverse Events (SAEs).
Ramy czasowe: Up to Month 48 and up to Month 84
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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.
A related SAE was defined as an event assessed by the investigator as causally related to the study vaccination.
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Up to Month 48 and up to Month 84
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Number of Subjects Reporting Related or Fatal Serious Adverse Event.
Ramy czasowe: Up to Month 84
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Serious adverse events (SAEs) assessed include medical occurrences that result in death, are life threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity.
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Up to Month 84
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Number of Subjects Reporting Any AE/SAE Leading to Premature Discontinuation of the Study.
Ramy czasowe: Up to Month 84
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An unsolicited AE covers any untoward medical occurrence in a clinical investigation subject temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product and 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. Serious adverse events (SAEs) assessed include medical occurrences that result in death, are life threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity. |
Up to Month 84
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Number of Subjects Reporting New Onset of Chronic Disease (NOCDs).
Ramy czasowe: Up to Month 48
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NOCDs include autoimmune disorders, asthma and type I diabetes.
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Up to Month 48
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Number of Subjects Reporting New Onset of Autoimmune Disease (NOADs).
Ramy czasowe: Up to Month 48
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Up to Month 48
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Number of Subjects Reporting Medically Significant Conditions (MAEs).
Ramy czasowe: Up to Month 48
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Medically significant conditions were defined as: AEs prompting emergency room or physician visits that were not (1) related to common diseases or (2) routine visits for physical examination or vaccination, or SAEs that were not related to common diseases.
Common diseases included: upper respiratory infections, sinusitis, pharyngitis, gastroenteritis, urinary tract infections, cervicovaginal yeast infections, menstrual cycle abnormalities and injury.
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Up to Month 48
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Number of Subjects With Pregnancies and Their Outcomes.
Ramy czasowe: Up to Month 48
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Pregnancy outcomes are live infant, premature live infant, elective termination, ectopic pregnancy, spontaneous abortion, lost to follow-up and pregnancy ongoing.
For each category it was specified if the infant presents congenital anomaly (CA) or no apparent congenital anomaly (No ACA).
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Up to Month 48
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Using the Type Assignment Algorithm (TAA)
Ramy czasowe: Up to Month 48
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer. Detection was done on subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline. TAA: Type assignment algorithm. The lesion was assigned to an HPV type found in the lesion if
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Up to Month 48
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18
Ramy czasowe: Up to Month 84
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
Detection was done in: - DNA- and sero-/+: subjects HPV DNA negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative/positive (sero-/+) for HPV-16 and/or HPV-18 by ELISA at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
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Up to Month 84
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Number of Subjects With Persistent Infection (12-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18
Ramy czasowe: Up to Month 84
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Persistent cervical HPV infection (12-month definition) was defined as the detection of the same HPV type(s) PCR in cervical samples at all available time points over approximately a 12-month interval (evaluations are planned at approximately 6-month intervals).
- DNA- and sero-/+: subjects HPV DNA negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative/positive (sero-/+) for HPV-16 and/or HPV-18 by ELISA at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
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Up to Month 84
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Number of Subjects With Persistent Infection (6-month Definition) With Oncogenic HPV Types Individually or in Combinations.
Ramy czasowe: Up to Month 84
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Persistent cervical HPV infection (6-month definition) = detection of the same HPV type(s) by PCR in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68.
Detection was done in subjects HPV DNA- for the corresponding HPV type at baseline (at month 0 and Month 6) regardless of initial serostatus.
HPV-HRW=All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18.
HPV-HR=High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68.
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Up to Month 84
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Number of Subjects With Persistent Infection (12-month Definition) With Oncogenic HPV Types Individually or in Combinations.
Ramy czasowe: Up to Month 84
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Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68.
subjects HPV DNA- for the corresponding HPV type at Month 0 6, regardless of initial serostatus.
HPV-HRW=All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18 HPV-HR=High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 , 68
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Up to Month 84
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)2+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 84
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CIN2+ was defined as CIN grades 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer.
Detection was done in: - DNA- and sero-: subjects HPV deoxyribonucleic acid (DNA) negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative (sero-) for HPV-16 and/or HPV-18 by Enzyme-linked Immunosorbent Assay (ELISA) at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
Note: Results for seropositive status were not analysed.
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Up to Month 84
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 84
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer.
Detection was done in: - DNA- and sero-/+: subjects HPV deoxyribonucleic acid (DNA) negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative/positive (sero-/+) for HPV-16 and/or HPV-18 by Enzyme-linked Immunosorbent Assay (ELISA) at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
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Up to Month 84
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Within the Lesional Component of the Cervical Tissue Specimen
Ramy czasowe: Up to Month 84
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Up to Month 84
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Number of Subjects With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Irrespective of HPV Cervical Infection and Irrespective of Baseline HPV DNA Status
Ramy czasowe: Up to Month 84
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CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer.
Detection was done on all subjects irrespective of their baseline HPV DNA status.
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Up to Month 84
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Number of Subjects With Any Cytological Abnormalities Associated With HPV-16 or HPV-18 Cervical Infection
Ramy czasowe: Up to Month 84
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Cytological abnormalities = atypical squamous cells of undetermined significance (ASC-US).
Detection was done in: - DNA- and sero-: subjects HPV deoxyribonucleic acid (DNA) negative (DNA-) at Month 0 and Month 6 for the corresponding HPV-type and seronegative (sero-) for HPV-16 and/or HPV-18 by Enzyme-linked Immunosorbent Assay (ELISA) at baseline (Month 0). - Overall: subjects DNA- at Month 0 and Month 6 for the corresponding HPV-type and regardless of initial serostatus at baseline.
Results for seropositive status were not analysed.
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Up to Month 84
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Number of Subjects With Cytological Abnormalities Associated With Oncogenic HPV Types Individually or in Combinations
Ramy czasowe: Up to Month 48
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Oncogenic HPV types included HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68.
Detection was done in subjects who were HPV DNA negative for the corresponding HPV type at baseline (at month 0 and Month 6) regardless of initial serostatus.
HRW-HPV= All high-risk (oncogenic) HPV types excluding HPV-16 and HPV-18 HPV-HR= High-risk (oncogenic) HPV types: HPV-16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68
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Up to Month 48
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Number of Subjects With Histopathologically Confirmed Reduction of Local Cervical Therapy
Ramy czasowe: Up to Month 84
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Detection was done on all subjects irrespective of their baseline HPV DNA status.
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Up to Month 84
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Number of Subjects With First Colposcopy
Ramy czasowe: Up to Month 84
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Detection was done on all subjects irrespective of their baseline HPV DNA status.
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Up to Month 84
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Number of Subjects With Persistent Infection (6-month Definition) With Human Papillomavirus (HPV)-16 or HPV-18 and/or With Histopathologically-confirmed Cervical Intraepithelial Neoplasia (CIN)1+ Associated With HPV-16 and/or -18 Cervical Infection
Ramy czasowe: Up to Month 84
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
CIN1+ was defined as CIN grades 1, 2 and 3, adenocarcinoma in situ (AIS) and invasive cervical cancer.
Detection was done on all subjects irrespective of their baseline HPV DNA and serostatus.
|
Up to Month 84
|
|
Number of Subjects With Persistent Infection (6-month Definition) With HPV-16 or HPV-18 and/or With Histopathologically-confirmed CIN1+ Associated With HPV-16 and/or -18 Cervical Infection Detected Using the HPV Type Assignment Algorithm (TAA).
Ramy czasowe: Up to Month 84
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Persistent cervical HPV infection (6-month definition) was defined as the detection of the same HPV type(s) by polymerase chain reaction (PCR) in cervical samples at 2 consecutive evaluations over approximately a 6-month interval.
Detection was done on all subjects irrespective of their baseline HPV DNA and serostatus.
The lesion was assigned to an HPV type found in the lesion if (1) the same HPV type was found in at least 1 of the 2 (closest) preceding cytology samples, or (2) none of the HPV types found in the lesion were found in any of the 2 preceding cytology samples (isolate HPV types)
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Up to Month 84
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Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Publikacje i pomocne linki
Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.
Publikacje ogólne
- Verstraeten T, Descamps D, David MP, Zahaf T, Hardt K, Izurieta P, Dubin G, Breuer T. Analysis of adverse events of potential autoimmune aetiology in a large integrated safety database of AS04 adjuvanted vaccines. Vaccine. 2008 Dec 2;26(51):6630-8. doi: 10.1016/j.vaccine.2008.09.049.
- Chen J, Gopala K, Akarsh PK, Struyf F, Rosillon D. Prevalence and Incidence of Human Papillomavirus (HPV) Infection Before and After Pregnancy: Pooled Analysis of the Control Arms of Efficacy Trials of HPV-16/18 AS04-Adjuvanted Vaccine. Open Forum Infect Dis. 2019 Dec 4;6(12):ofz486. doi: 10.1093/ofid/ofz486. eCollection 2019 Dec. Erratum In: Open Forum Infect Dis. 2020 Feb 28;7(3):ofaa036.
- Descamps D, Hardt K, Spiessens B, Izurieta P, Verstraeten T, Breuer T, Dubin G. Safety of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine for cervical cancer prevention: a pooled analysis of 11 clinical trials. Hum Vaccin. 2009 May;5(5):332-40. doi: 10.4161/hv.5.5.7211. Epub 2009 May 20.
- Skinner SR, Szarewski A, Romanowski B, Garland SM, Lazcano-Ponce E, Salmeron J, Del Rosario-Raymundo MR, Verheijen RH, Quek SC, da Silva DP, Kitchener H, Fong KL, Bouchard C, Money DM, Ilancheran A, Cruickshank ME, Levin MJ, Chatterjee A, Stapleton JT, Martens M, Quint W, David MP, Meric D, Hardt K, Descamps D, Geeraerts B, Struyf F, Dubin G; VIVIANE Study Group. Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 4-year interim follow-up of the phase 3, double-blind, randomised controlled VIVIANE study. Lancet. 2014 Dec 20;384(9961):2213-27. doi: 10.1016/S0140-6736(14)60920-X. Epub 2014 Sep 1.
- Wheeler CM, Skinner SR, Del Rosario-Raymundo MR, Garland SM, Chatterjee A, Lazcano-Ponce E, Salmeron J, McNeil S, Stapleton JT, Bouchard C, Martens MG, Money DM, Quek SC, Romanowski B, Vallejos CS, Ter Harmsel B, Prilepskaya V, Fong KL, Kitchener H, Minkina G, Lim YKT, Stoney T, Chakhtoura N, Cruickshank ME, Savicheva A, da Silva DP, Ferguson M, Molijn AC, Quint WGV, Hardt K, Descamps D, Suryakiran PV, Karkada N, Geeraerts B, Dubin G, Struyf F; VIVIANE Study Group. Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 7-year follow-up of the phase 3, double-blind, randomised controlled VIVIANE study. Lancet Infect Dis. 2016 Oct;16(10):1154-1168. doi: 10.1016/S1473-3099(16)30120-7. Epub 2016 Jun 28.
- Wheeler CM, Struyf F; HPV-015 study group. The safety of Cervarix? - Authors' reply. Lancet Infect Dis. 2017 Jan;17(1):20-21. doi: 10.1016/S1473-3099(16)30540-0. No abstract available.
- Rosillon D, Baril L, Del Rosario-Raymundo MR, Wheeler CM, Skinner SR, Garland SM, Salmeron J, Lazcano-Ponce E, Vallejos CS, Stoney T, Ter Harmsel B, Lim TYK, Quek SC, Minkina G, McNeil SA, Bouchard C, Fong KL, Money D, Ilancheran A, Savicheva A, Cruickshank M, Chatterjee A, Fiander A, Martens M, Bozonnat MC, Struyf F, Dubin G, Castellsague X. Risk of newly detected infections and cervical abnormalities in adult women seropositive or seronegative for naturally acquired HPV-16/18 antibodies. Cancer Med. 2019 Aug;8(10):4938-4953. doi: 10.1002/cam4.1879. Epub 2019 Jul 5.
- Skinner SR, Wheeler CM, Romanowski B, Castellsague X, Lazcano-Ponce E, Del Rosario-Raymundo MR, Vallejos C, Minkina G, Pereira Da Silva D, McNeil S, Prilepskaya V, Gogotadze I, Money D, Garland SM, Romanenko V, Harper DM, Levin MJ, Chatterjee A, Geeraerts B, Struyf F, Dubin G, Bozonnat MC, Rosillon D, Baril L; VIVIANE Study Group. Progression of HPV infection to detectable cervical lesions or clearance in adult women: Analysis of the control arm of the VIVIANE study. Int J Cancer. 2016 May 15;138(10):2428-38. doi: 10.1002/ijc.29971.
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
16 lutego 2006
Zakończenie podstawowe (Rzeczywisty)
29 stycznia 2014
Ukończenie studiów (Rzeczywisty)
29 stycznia 2014
Daty rejestracji na studia
Pierwszy przesłany
17 lutego 2006
Pierwszy przesłany, który spełnia kryteria kontroli jakości
17 lutego 2006
Pierwszy wysłany (Oszacować)
20 lutego 2006
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
2 stycznia 2020
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
27 grudnia 2019
Ostatnia weryfikacja
1 grudnia 2019
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 104820
- 2005-002546-20 (Numer EudraCT)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
TAK
Opis planu IPD
IPD is available via the Clinical Study Data Request site (click on the link provided below)
Ramy czasowe udostępniania IPD
IPD is available via the Clinical Study Data Request site (click on the link provided below)
Kryteria dostępu do udostępniania IPD
Access is provided after a research proposal is submitted and has received approval from the Independent Review Panel and after a Data Sharing Agreement is in place.
Access is provided for an initial period of 12 months but an extension can be granted, when justified, for up to another 12 months.
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ICF
- CSR
Badanie danych/dokumentów
-
Formularz świadomej zgody
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
-
Raport z badania klinicznego
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
-
Protokół badania
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
-
Specyfikacja zestawu danych
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
-
Indywidualny zestaw danych uczestnika
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
-
Plan analizy statystycznej
Identyfikator informacji: 104820Komentarze do informacji: For additional information about this study please refer to the GSK Clinical Study Register
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .