Last updated: 11/07/2018 03:38:54
A trial to test the response to different vaccination regimens with an H5N1 vaccine with AS03 in adults aged 18-64
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A trial to evaluate the immunogenicity of accelerated primary vaccination with monovalent A/Indonesia/5/05 (H5N1) vaccine antigen in association with AS03 adjuvant in adults aged 18-64
Trial description: The purpose of the study is to characterize the immunogenicity & safety of 2 doses of GSK’s avian flu vaccine GSK 1557484A given according to different regimens to adults aged 18 to 64 years
Primary purpose:
Prevention
Trial design:
Parallel Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:
Number of seroconverted subjects against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Day 14 post Dose 2
Titers for serum hemagglutination inhibition (HI) antibodies against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Day 0 and at Day 14 post Dose 2
Number of seroprotected subjects against 3 strains the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Day 0 and at Day 14 post Dose 2
Secondary outcomes:
Titers for serum hemagglutination inhibition (HI) antibodies against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Days 0, 21, 28, 35, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Days 0, 14, 21, 28, 35, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 28, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the A/Indonesia/5/2005 (H5N1) strain of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 21, 28, 35, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 14, 21, 28, 35, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 28, 42 and 182.
Titers for serum hemagglutination inhibition (HI) antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 42 and 182.
Number of seroconverted subjects against the A/Indonesia/5/2005 (H5N1), Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Day 42
Number of seroconverted subjects against the A/Indonesia/5/2005 (H5N1) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Day 182
Geometric mean fold-rise (GMFR) for the A/Indonesia/5/2005 (H5N1), Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 42 and 182.
Micro-neutralization (MN) titers for antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 21, 28, 35, 42 and 182.
Micro-neutralization (MN) titers for antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 14, 21, 28, 35, 42 and 182.
Micro-neutralization (MN) titers for antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 28, 42 and 182.
Micro-neutralization (MN) titers for antibodies against the Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Days 0, 7, 14, 21, 42 and 182.
Number of subjects with a vaccine response of MN assessed antibodies for Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At 7, 14 and 21 days after the second dose
Number of subjects with a vaccine response of MN assessed antibodies for Flu A/Vietnam/1194/2004 (VIET) and Flu A/turkey/Turkey/1/2005 (TURK) strains of influenza disease.
Timeframe: At Day 42
Number of subjects with a vaccine response of MN assessed antibodies for the Flu A/turkey/Turkey/1/2005 (TURK) strain of influenza disease.
Timeframe: At Day 182
Number of subjects with solicited local symptoms
Timeframe: Within the 7-day follow-up period (Days 0-6) after any vaccination
Number of subjects with solicited general symptoms
Timeframe: Within the 7-day follow-up period (Days 0-6) after any vaccination
Number of subjects with medically attended adverse events (MAEs).
Timeframe: From Day 0 to 182
Number of subjects with unsolicited adverse events (AEs)
Timeframe: Within the 51-day follow-up period (Days 0-50) after first vaccination.
Number of subjects with any serious adverse events (SAEs)
Timeframe: From Day 0 to 182
Interventions:
Enrollment:
312
Primary completion date:
2008-13-08
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Langley JM et al. (2010) Safety and cross-reactive immunogenicity of candidate AS03-adjuvanted prepandemic H5N1 influenza vaccines: a randomized controlled phase 1/2 trial in adults. J Infect Dis. 201(11):1644–1653.
Medical condition
Influenza
Product
GSK1557484A
Collaborators
Not applicable
Study date(s)
June 2008 to January 2009
Type
Interventional
Phase
2
Participation criteria
Sex
Female & Male
Age
18 - 64 years
Accepts healthy volunteers
Yes
- A male or female 18-64 years old at the time of the first vaccination.
- Written informed consent obtained from the subject.
- Presence of evidence of substance abuse or of neurological or psychiatric diagnoses which, even if clinically stable, are deemed by the investigator to render the potential subject unable/unlikely to provide accurate safety reports.
- Diagnosed with cancer, or treatment for cancer, within 3 years.
Inclusion and exclusion criteria
Inclusion criteria:
- A male or female 18-64 years old at the time of the first vaccination.
- Written informed consent obtained from the subject.
- Good general health as established by medical history and clinical examination before entering into the study.
- Access to a consistent means of telephone contact.
- Comprehension of the study requirements, ability to comprehend and comply with procedures for collection of short- and long-term safety data, expressed availability for the required study period, and ability and willingness to attend scheduled visits.
- Subjects who the investigator believes that they can and will comply with the requirements of the protocol should be enrolled in the study
Exclusion criteria:
- Presence of evidence of substance abuse or of neurological or psychiatric diagnoses which, even if clinically stable, are deemed by the investigator to render the potential subject unable/unlikely to provide accurate safety reports.
- Diagnosed with cancer, or treatment for cancer, within 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 histologically-confirmed basal cell carcinoma of the skin successfully treated with local excision only are excepted and may be enrolled, but other histological types of skin cancer are exclusionary.
- Women who are disease-free 3 years or more after treatment for breast cancer and receiving long-term prophylactic tamoxifen are excepted and may be enrolled.
- Presence of an oral temperature ≥37.8ºC, or acute symptoms greater than "mild" severity on the scheduled date of first vaccination.
- Any confirmed or suspected immunosuppressive or immunodeficient condition including history of human immunodeficiency virus (HIV) infection.
- Receipt of systemic glucocorticoids within 1 month of study enrollment, or any other cytotoxic or immunosuppressive drug within 6 months of study enrollment.
- Any significant disorder of coagulation or treatment with Coumadin derivatives or heparin.
- Administration of any vaccines within 30 days before study enrollment or during the 30 days following the last test article dose. Subjects who receive such immunizations on an emergent basis after enrollment will be followed per protocol and included in the Total Vaccinated Cohort (TVC), but excluded from the According to Protocol (ATP) Cohort for both safety and immunogenicity.
- Previous administration of any H5N1 vaccine.
- Use of any investigational or non-registered product (drug or vaccine) or planned participation in another investigational study within 30 days prior to study enrollment, or during the 182 days following the first test article dose. Use of any investigational or non-registered product with immunosuppressive properties is exclusionary at any time during the trial.
- Receipt of any immunoglobulins and/or any blood products within 6 months of study enrollment or planned administration of any of these products during the study period.
- Any known or suspected allergy to any constituent of influenza vaccines (including egg proteins or mercurial preservatives); a history of anaphylactic-type reaction to consumption of eggs; or a history of severe adverse reaction to a previous influenza vaccine.
- Known pregnancy or a positive urine beta-human chorionic gonadotropin (β-hCG) test result prior to either vaccination.
- Lactating or nursing.
- Women of child bearing potential who lack a history of reliable contraceptive practices. The provision of this history does NOT replace the requirement to perform, and obtain negative results in pregnancy urine tests prior to treatments. Note: all women will have urine pregnancy tests regardless of their status.
- Known receipt of analgesic or antipyretic medication on the day of treatment with specific intent of prophylaxis of vaccine reactogenicity on the day of first or any treatment. Subjects on stable chronic regimens of potentially analgesic or anti-pyretic medications for pre-existing diagnoses are not required to discontinue them
Trial location(s)
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2008-13-08
Actual study completion date
2009-08-01
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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