- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT00968526
Study to Evaluate Immunogenicity and Safety of an Investigational Influenza Vaccine (H1N1) in Adults
11 juni 2019 bijgewerkt door: 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.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
240
Fase
- Fase 3
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
-
-
-
Wilrijk, België, 2610
- GSK Investigational Site
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of Seroconverted (SCR) Subjects for Hemagglutination Inhibition (HI) Antibodies
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of Subjects Who Were Seropositive for HI Antibodies Against the Flu A/California/7/2009 (H1N1) Virus Strain
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Algemene publicaties
- 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.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
8 september 2009
Primaire voltooiing (Werkelijk)
23 september 2010
Studie voltooiing (Werkelijk)
23 september 2010
Studieregistratiedata
Eerst ingediend
27 augustus 2009
Eerst ingediend dat voldeed aan de QC-criteria
27 augustus 2009
Eerst geplaatst (Schatting)
31 augustus 2009
Updates van studierecords
Laatste update geplaatst (Werkelijk)
25 juni 2019
Laatste update ingediend die voldeed aan QC-criteria
11 juni 2019
Laatst geverifieerd
1 juni 2019
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 113459
- 2009-013837-92 (EudraCT-nummer)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Ja
Beschrijving IPD-plan
IPD for this study will be made available via the Clinical Study Data Request site.
IPD-tijdsbestek voor delen
IPD is available via the Clinical Study Data Request site (click on the link provided below)
IPD-toegangscriteria voor delen
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.
IPD delen Ondersteunend informatietype
- Leerprotocool
- Statistisch Analyse Plan (SAP)
- Formulier voor geïnformeerde toestemming (ICF)
- Klinisch onderzoeksrapport (CSR)
Bestudeer gegevens/documenten
-
Statistisch analyseplan
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Gegevensset individuele deelnemers
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Leerprotocool
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Specificatie gegevensset
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Geannoteerd casusrapportformulier
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Klinisch onderzoeksrapport
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
-
Formulier geïnformeerde toestemming
Informatie-ID: 113459Informatie opmerkingen: For additional information about this study please refer to the GSK Clinical Study Register
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .