- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00968526
Study to Evaluate Immunogenicity and Safety of an Investigational Influenza Vaccine (H1N1) in Adults
11. června 2019 aktualizováno: GlaxoSmithKline
Safety and Immunogenicity Study of GSK Biologicals' Influenza Vaccine GSK2340272A in Adults Aged 18 Years and Above
The objective of the study is to evaluate the immunogenicity and safety of GSK Biologicals' investigational vaccine GSK2340272A.
Přehled studie
Postavení
Dokončeno
Podmínky
Intervence / Léčba
Typ studie
Intervenční
Zápis (Aktuální)
240
Fáze
- Fáze 3
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní místa
-
-
-
Wilrijk, Belgie, 2610
- GSK Investigational Site
-
-
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
18 let a starší (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Popis
Inclusion Criteria:
- A male or female aged 18 years or above at the time of the first vaccination.
- Subjects who the investigator believes that they can and will comply with the requirements of the protocol.
- Written informed consent obtained from the subject.
- Satisfactory baseline medical assessment by history and physical examination. Stable health status is defined as the absence of a health event satisfying the definition of a serious adverse event, or a change in an ongoing drug therapy due to therapeutic failure or symptoms of drug toxicity, within one month prior to enrolment.
- Access to a consistent means of telephone contact, which may be either in the home or at the workplace, land line or mobile, but NOT a pay phone or other multiple-user device.
- 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 2 months after completion of the vaccination series.
Exclusion Criteria:
- Use of any investigational or non-registered product other than the study vaccine within 30 days preceding the first dose of the study vaccine or planned use during the study period. Potential subjects in the follow-up phase of a prior investigational study may be enrolled if the investigator's judgment is that it will have no effect on safety, reactogenicity, or immunogenicity endpoints in this study, and that it does not violate the protocol requirements of the prior trial.
- Presence of evidence of substance abuse or of neurological or psychiatric diagnoses which, although stable, are deemed by the investigator to render the potential subject unable/unlikely to provide accurate safety reports.
- Presence of an axillary temperature >= 37.5ºC, or acute symptoms greater than "mild" severity on the scheduled date of first vaccination. NOTE: The subject may be vaccinated at a later date, provided symptoms have resolved, vaccination occurs within the window specified by the protocol, and all other eligibility criteria continue to be satisfied.
- Diagnosed with cancer, or treatment for cancer, within the past 3 years.
- Persons with a history of cancer who are disease-free without treatment for 3 years or more are eligible.
- Persons with a history of histological-confirmed basal cell carcinoma of the skin successfully treated with local excision only are excepted and may enrol within 3 years of diagnosis, but other histological types of skin cancer require a 3-year untreated and disease-free window as above.
- Women who are disease-free 3 years or more after treatment for breast cancer and receiving long-term prophylactic hormonal therapy are excepted and may enrol.
- Any confirmed or suspected immunosuppressive or immunodeficient condition including history of human immunodeficiency virus (HIV) infection.
- Chronic administration of immunosuppressants or other immune modifying drugs within 6 months of study enrolment or planned administration during the study period.
- Receipt of any immunoglobulins and/or any blood products within 3 months of study enrolment or planned administration of any of these products during the study period.
- Any significant disorder of coagulation or treatment with warfarin derivatives or heparin. Persons receiving individual doses of low molecular weight heparin outside of 24 hours prior to vaccination are eligible. Persons receiving prophylactic antiplatelet medications, e.g., low-dose aspirin, and without a clinically-apparent bleeding tendency, are eligible.
- An acute evolving neurological disorder or history of Guillain-Barré syndrome.
- Clinically or virologically confirmed influenza infection within 6 months preceding the study start.
- Administration of any vaccines within 30 days before vaccination.
- Any known or suspected allergy to any constituent of influenza vaccines; anaphylactic-type reaction to any constituent of influenza vaccines; or a history of severe adverse reaction to a previous influenza vaccine.
- Pregnant or lactating female
- Female planning to become pregnant or planning to discontinue contraceptive precautions.
- Any conditions which, in the opinion of the investigator, prevents the subjects from participating in the study.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Primární účel: Prevence
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: GSK2340272A 2D Group
Healthy male or female adults, aged 18 to 60 years (18-60y) and above (>60y), who received two doses (2D) of GSK2340272A vaccine, one administered intramuscularly in the deltoid region of the non-dominant arm at Day 0 and the other one, administered intramuscularly in the deltoid region of the dominant arm at Day 21.
|
One or two intramuscular injections in the deltoid region of the non-dominant or the dominant arm.
|
|
Experimentální: GSK2340272A 1D Group
Healthy male or female adults, aged 18 to 60 years (18-60y) and above (>60y), who received a single dose (1D) of GSK2340272A vaccine, administered intramuscularly in the deltoid region of the non-dominant arm at Day 0.
|
One or two intramuscular injections in the deltoid region of the non-dominant or the dominant arm.
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Number of Seroconverted (SCR) Subjects for Hemagglutination Inhibition (HI) Antibodies
Časové okno: At Day 21
|
Seroconversion was defined as: For initially seronegative subjects [antibody titer (below) < 10 post-vaccination], antibody titer greater than or equal to (≥) 40 after vaccination; For initially seropositive subjects (antibody titer ≥ 10 prior to vaccination), antibody titer after vaccination ≥ 4 fold the pre-vaccination antibody titer.
The Flu strain assessed was A/California/7/2009 (H1N1)v-like influenza (Flu A/CAL/7/09).
This outcome included only subjects who received two doses of the study product and results were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age .
|
At Day 21
|
|
Number of Subjects Who Were Seroprotected (SPR) for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Časové okno: At Day 21
|
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:40, that usually is accepted as indicating protection.
This outcome included only subjects who received two doses of the study product and the results were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age .
|
At Day 21
|
|
Geometric Mean Fold Rise (GMFR) for HI Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Day 21
|
GMFR was defined as the fold change in serum HI geometric mean titers (GMTs) post-vaccination compared to pre-vaccination.
The flu strain assessed was Flu A/CAL/7/09.
This outcome included only subjects who received two doses of the study product and results were tabulated per age stratum.
The CHMP criterion was fulfilled if the point estimated for GMFR was > 2.5 in subjects 18 to 60 years old or > 2 for subjects > 60 years of age.
|
At Day 21
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Number of Subjects Who Were Seropositive for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Časové okno: At Days 0, 21 and 42
|
A seropositive subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:10, that usually is accepted as indicating protection.
The results for this assay were tabulated per age stratum.
|
At Days 0, 21 and 42
|
|
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Days 0, 21 and 42
|
Titers are presented as geometric mean titers (GMTs).
The flu strain assessed was Flu A/CAL/7/09.
The reference seropositivity cut-off value was ≥ 1:10.
The results for this assay were tabulated per age stratum.
|
At Days 0, 21 and 42
|
|
Number of Subjects Who Were Seropositive for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Časové okno: At Day 182 and 364
|
A seropositive subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:10, that usually is accepted as indicating protection.
The results for this assay were tabulated per age stratum.
|
At Day 182 and 364
|
|
Titers for Serum Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Day 182 and 364
|
Titers are presented as geometric mean titers (GMTs).
The flu strain assessed was Flu A/CAL/7/09.
The reference seropositivity cut-off value was ≥ 1:10.
The results for this assay were tabulated per age stratum.
|
At Day 182 and 364
|
|
Number of Seroconverted (SCR) Subjects for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/2009 Strain of Influenza Disease
Časové okno: At Days 21 and 42
|
Seroconversion was defined as: For initially seronegative subjects [antibody titer below (<) 10 post to vaccination], antibody titer greater than or equal to (≥) 40 after vaccination; For initially seropositive subjects (antibody titer ≥ 10 prior to vaccination), antibody titer after vaccination ≥ 4 fold the pre-vaccination antibody titer.
The Flu strain assessed was A/California/7/2009 (H1N1)v-like influenza (Flu A/CAL/7/09).
This outcome included only subjects who received one dose of the study product and the results were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age .
|
At Days 21 and 42
|
|
Number of Seroconverted (SCR) Subjects for Hemagglutination Inhibition (HI) Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Days 182 and 364
|
Seroconversion was defined as: For initially seronegative subjects [antibody titer below (<) 10 post to vaccination], antibody titer greater than or equal to (≥) 40 after vaccination; For initially seropositive subjects (antibody titer ≥ 10 prior to vaccination), antibody titer after vaccination ≥ 4 fold the pre-vaccination antibody titer.
The Flu strain assessed was A/California/7/2009 (H1N1)v-like influenza (Flu A/CAL/7/09).
The results for this assay were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age .
|
At Days 182 and 364
|
|
Number of Subjects Who Were Seroprotected (SPR ) for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Časové okno: At Days 0, 21 and 42
|
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:40, that usually is accepted as indicating protection.
This outcome included only subjects who received one dose of the study product and the results were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age .
|
At Days 0, 21 and 42
|
|
Number of Subjects Who Were Seroprotected (SPR ) for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Časové okno: At Days 182 and 364
|
A seroprotected subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:40, that usually is accepted as indicating protection.
The results for this assay were tabulated per age stratum.
The CHMP criterion was fulfilled if the post-vaccination point estimate for SPR was > 70% in subjects 18 to 60 of age or > 60% for subjects above 60 years of age.
|
At Days 182 and 364
|
|
Geometric Mean Fold Rise (GMFR) for HI Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Days 21 and 42
|
GMFR was defined as the fold change in serum HI geometric mean titers (GMTs) post-vaccination compared to pre-vaccination.
The flu strain assessed was Flu A/CAL/7/09.
This outcome included only subjects who received one dose of the study product and the results were tabulated per age stratum.
The CHMP criterion was fulfilled if the point estimated for GMFR was > 2.5 in subjects 18 to 60 years old or > 2 for subjects > 60 years of age.
|
At Days 21 and 42
|
|
Geometric Mean Fold Rise (GMFR) for HI Antibodies Against Flu A/CAL/7/09 Strain of Influenza Disease
Časové okno: At Day 182 and 364
|
GMFR was defined as the fold change in serum HI geometric mean titers (GMTs) post-vaccination compared to pre-vaccination.
The flu strain assessed was Flu A/CAL/7/09.
The results for this assay were tabulated per age stratum.
The CHMP criterion was fulfilled if the point estimated for GMFR was > 2.5 in subjects 18 to 60 years old or > 2 for subjects > 60 years of age.
|
At Day 182 and 364
|
|
Number of Seropositive Subjects for Serum Neutralizing Antibodies Against Flu A/Netherlands (Neth)/602/09
Časové okno: At Days 0, 21, 42 and 182
|
A seropositive subject was defined as a vaccinated subject with a serum HI titer greater than or equal to (≥) 1:8, that usually is accepted as indicating protection.
The Flu strain assessed was Flu A/Neth/602/09.
The results for this assay were tabulated per age stratum.
|
At Days 0, 21, 42 and 182
|
|
Titers for Serum Neutralizing Antibodies Against Flu A/Neth/602/09 Strain of Influenza Disease
Časové okno: At Days 0, 21, 42 and 182
|
Titers are presented as geometric mean titers (GMTs).
The flu strain assessed was Flu A/Neth/602/09.
The reference seropositivity cut-off value was ≥ 1:8.
The results for this assay were tabulated per age stratum.
|
At Days 0, 21, 42 and 182
|
|
Number of Seroconverted Subjects for Serum Neutralizing Antibodies Against Flu A/Neth/602/09
Časové okno: At Days 21, 42 and 182
|
Seroconversion was defined as: For initially seronegative subjects, antibody titer ≥ 1:8 after vaccination; For initially seropositive subjects, antibody titer after vaccination ≥ 4 fold the pre-vaccination antibody titer.
The Flu strain assessed was Flu A/Neth/602/09.
The results were tabulated per age stratum.
|
At Days 21, 42 and 182
|
|
Number of Subjects With Any and Grade 3 Solicited Local Symptoms
Časové okno: During the 7-day (Days 0-6) post-dose 1 vaccination period
|
Assessed solicited local symptoms were pain, redness and swelling.
Any = occurrence of the symptom regardless of intensity grade.
Grade 3 pain = pain that prevented normal activity.
Grade 3 redness/swelling = redness/swelling spreading beyond 100 millimeters (mm) of injection site.
This outcome included all the subjects who received 1 dose of the study product and the assay results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-dose 1 vaccination period
|
|
Number of Days With Solicited Local Symptoms
Časové okno: During the 7-day (Days 0-6) post-dose 1 vaccination period
|
The number of days with any solicited local symptoms reported during the solicited post-vaccination period.
This outcome included all the subjects who received 1 dose of the study product and the assay results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-dose 1 vaccination period
|
|
Number of Subjects With Any and Grade 3 Solicited Local Symptoms
Časové okno: During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
Assessed solicited local symptoms were pain, redness and swelling.
Any = occurrence of the symptom regardless of intensity grade.
Grade 3 pain = pain that prevented normal activity.
Grade 3 redness/swelling = redness/swelling spreading beyond 100 millimeters (mm) of injection site.
This outcome included only subjects who received two doses of the study product and the results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
|
Number of Days With Solicited Local Symptoms
Časové okno: During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
The number of days with any solicited local symptoms reported during the solicited post-vaccination period.
This outcome included only subjects who received 2 doses of the study product and the results were tabulated per age stratum.
No subjects from GSK2340272A 2D (18-60y) Sub-Group presented any redness post dose 1.
|
During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
|
Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms
Časové okno: During the 7-day (Days 0-6) post-dose 1 vaccination period
|
Assessed solicited general symptoms were fatigue, headache, joint pain at other location, muscle aches, shivering, sweating and fever [defined as axillary temperature equal to or above (>) 37.5 degrees Celsius (°C)].
Any = occurrence of the symptom regardless of intensity grade.
Grade 3 symptom = symptom that prevented normal activity.
Grade 3 fever = temperature ≥ 39.0 °C.
Related = symptom assessed by the investigator as related to the vaccination.
This outcome included all the subjects who received 1 dose of the study product and the assay results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-dose 1 vaccination period
|
|
Number of Days With Solicited General Symptoms
Časové okno: During the 7-day (Days 0-6) post-dose 1 vaccination period
|
The number of days with any solicited general symptoms reported during the solicited post-vaccination period.
This outcome included all the subjects who received 1 dose of the study product and the results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-dose 1 vaccination period
|
|
Number of Subjects With Any, Grade 3 and Related Solicited General Symptoms
Časové okno: During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
Assessed solicited general symptoms were fatigue, headache, joint pain at other location, muscle aches, shivering, sweating and fever [defined as axillary temperature above (>) 37.5 degrees Celsius (°C)].
Any = occurrence of the symptom regardless of intensity grade.
Grade 3 symptom = symptom that prevented normal activity.
Grade 3 fever = temperature ≥ 39.0 °C.
Related = symptom assessed by the investigator as related to the vaccination.
This outcome inlcuded only subjects who received two doses of the study product and the results were tabulated per age stratum.
|
During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
|
Number of Days With Solicited General Symptoms
Časové okno: During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
The number of days with any solicited general symptoms reported during the solicited post-vaccination period.
This outcome included only subjects who received two doses of the study product and the results were tabulated per age stratum.
No subjects from GSK2340272A 2D (>60y) Sub-Group reported any temperature.
|
During the 7-day (Days 0-6) post-vaccination period following each dose and across doses
|
|
Number of Subjects With Adverse Events of Specific Interest (AESIs)
Časové okno: During the entire study period (from Day 0 up to Day 364)
|
An AESI was defined as an AE including autoimmune diseases and other mediated inflammatory disorders and assessed by the investigator as specific to the treatment administration.
The results were tabulated per age stratum.
|
During the entire study period (from Day 0 up to Day 364)
|
|
Number of Subjects With Normal/Abnormal Biochemical and Haematological Levels
Časové okno: At Days 0, 21, 42, 182 and 364
|
Among biochemical and haematological parameters assessed were alanine aminotransferase [ALT], alkaline phosphatase [AP], aspartate aminotransferase [AST], total bilirubin [BIL], creatinine [CRE], blood urea nitrogen [BUN].
Levels of haematological/biochemical parameters assessed with respect to normal laboratory values were - unknown, below, within and above in subjects aged 18-60 years and > 60 years old.
|
At Days 0, 21, 42, 182 and 364
|
|
Number of Subjects With Any, Grade 3 and Related Unsolicited Adverse Events (AEs)
Časové okno: Within 21 days after the first vaccination (Day 0 - Day 20)
|
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.
Any was defined as the occurrence of any unsolicited AE regardless of intensity grade or relation to vaccination.
Grade 3 AE = an AE which prevented normal, everyday activities.
Related = AE assessed by the investigator as related to the vaccination.
This outcome included all the subjects who received 1 dose of the study product and the results were tabulated per age stratum.
|
Within 21 days after the first vaccination (Day 0 - Day 20)
|
|
Number of Subjects With Any, Grade 3 and Related Unsolicited Adverse Events (AEs)
Časové okno: Within 84 days after the first vaccination and 63 days after the second vaccination (Day 0 - Day 83)
|
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.
Any was defined as the occurrence of any unsolicited AE regardless of intensity grade or relation to vaccination.
Grade 3 AE = an AE which prevented normal, everyday activities.
Related = AE assessed by the investigator as related to the vaccination.
The results were tabulated per age stratum.
|
Within 84 days after the first vaccination and 63 days after the second vaccination (Day 0 - Day 83)
|
|
Number of Subjects With Serious Adverse Events (SAEs)
Časové okno: During the entire study period (from Day 0 up to Day 364)
|
SAEs assessed include medical occurrences that result in death, are life-threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity.
The results were tabulated per age stratum.
|
During the entire study period (from Day 0 up to Day 364)
|
Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Obecné publikace
- Van Damme P, Kafeja F, Bambure V, Hanon E, Moris P, Roman F, Gillard P. Long-term persistence of humoral and cellular immune responses induced by an AS03A-adjuvanted H1N1 2009 influenza vaccine: an open-label, randomized study in adults aged 18-60 years and older. Hum Vaccin Immunother. 2013 Jul;9(7):1512-22. doi: 10.4161/hv.24504. Epub 2013 Apr 9.
- Roman F, Vaman T, Kafeja F, Hanon E, Van Damme P. AS03(A)-Adjuvanted influenza A (H1N1) 2009 vaccine for adults up to 85 years of age. Clin Infect Dis. 2010 Sep 15;51(6):668-77. doi: 10.1086/655830.
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia (Aktuální)
8. září 2009
Primární dokončení (Aktuální)
23. září 2010
Dokončení studie (Aktuální)
23. září 2010
Termíny zápisu do studia
První předloženo
27. srpna 2009
První předloženo, které splnilo kritéria kontroly kvality
27. srpna 2009
První zveřejněno (Odhad)
31. srpna 2009
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
25. června 2019
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
11. června 2019
Naposledy ověřeno
1. června 2019
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- 113459
- 2009-013837-92 (Číslo EudraCT)
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Ano
Popis plánu IPD
IPD for this study will be made available via the Clinical Study Data Request site.
Časový rámec sdílení IPD
IPD is available via the Clinical Study Data Request site (click on the link provided below)
Kritéria přístupu pro sdílení 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 podpůrných informací pro sdílení IPD
- Protokol studie
- Plán statistické analýzy (SAP)
- Formulář informovaného souhlasu (ICF)
- Zpráva o klinické studii (CSR)
Studijní data/dokumenty
-
Plán statistické analýzy
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Soubor dat jednotlivých účastníků
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Protokol studie
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Specifikace datové sady
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Formulář komentované zprávy o případu
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Zpráva o klinické studii
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
-
Formulář informovaného souhlasu
Identifikátor informace: 113459Komentáře k informacím: For additional information about this study please refer to the GSK Clinical Study Register
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na GSK investigational vaccine GSK2340272A
-
GlaxoSmithKlineThe PATH Malaria Vaccine Initiative (MVI)Dokončeno
-
GlaxoSmithKlineDokončeno