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Study to Evaluate Immunogenicity & Safety of an Investigational Influenza Vaccine in Adults

This study has been completed.
Sponsor:
Information provided by:
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00975884
First received: September 11, 2009
Last updated: January 5, 2012
Last verified: February 2011

September 11, 2009
January 5, 2012
September 2009
April 2010   (final data collection date for primary outcome measure)
Humoral immune response in terms of haemagglutination inhibition (HI) antibodies [ Time Frame: At Day 21 ] [ Designated as safety issue: No ]
Humoral immune response in terms of haemagglutination inhibition (HI) antibodies [ Time Frame: At Day 42 ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00975884 on ClinicalTrials.gov Archive Site
  • Occurrence of local and general symptoms [ Time Frame: During a 7-day (day 0-6) follow-up period after vaccination ] [ Designated as safety issue: No ]
  • Occurrence of serious adverse events [ Time Frame: During the entire study period (Day 0 - Day 364) ] [ Designated as safety issue: No ]
  • Humoral immune response in terms of HI antibodies [ Time Frame: At Day 0, 21, 42, 182, 203 (only for group B) and 364 ] [ Designated as safety issue: No ]
  • Humoral immune response in terms of neutralizing antibodies [ Time Frame: At Day 0, 21, 42, 182, 203 (only for group B) and 364 ] [ Designated as safety issue: No ]
  • Occurrence of adverse events of specific and special interest [ Time Frame: During the entire study period (Day 0 - Day 364) ] [ Designated as safety issue: No ]
  • Safety evaluation in terms of biochemical parameters (Blood Urea Nitrogen, Alanine Aminotransferase, Aspartate Aminotransferase, Alkaline phosphatase, Bilirubin, and Creatinine) [ Time Frame: At Day 0, 21, 42, 182, 203 (only for group B) and 364 ] [ Designated as safety issue: No ]
  • Occurence of unsolicited symptoms [ Time Frame: During a 21- day (Day 0 - 20) follow-up period after vaccination ] [ Designated as safety issue: No ]
  • Humoral immune response in terms of HI antibodies [ Time Frame: At Day 0, 21, 42, 182 and 364 ] [ Designated as safety issue: No ]
  • Humoral immune response in terms of neutralizing antibodies [ Time Frame: At Day 0, 21, 42, 182 and 364 ] [ Designated as safety issue: No ]
  • Occurrence of local and general symptoms [ Time Frame: During a 7-day (day 0-6) follow-up period after vaccination ] [ Designated as safety issue: No ]
  • Occurrence of unsolicited symptoms [ Time Frame: During a 21-day (day 0-20) follow-up period after vaccination ] [ Designated as safety issue: No ]
  • Occurrence of adverse events of specific interest [ Time Frame: During the entire study period (Day 0 - Day 364) ] [ Designated as safety issue: No ]
  • Occurrence of serious adverse events [ Time Frame: During the entire study period (Day 0 - Day 364) ] [ Designated as safety issue: No ]
  • Safety evaluation in terms of biochemical parameters [ Time Frame: At Day 0, 21, 42, 182 and 364 ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Study to Evaluate Immunogenicity & Safety of an Investigational Influenza Vaccine in Adults
Safety and Immunogenicity Study of GSK Biologicals' Influenza Vaccine GSK2340272A in Adults Aged 18 Years and Above

The objective of this study is to evaluate the immunogenicity and safety of GSK Biologicals' investigational vaccine GSK2340272A.

Not Provided
Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
  • Influenza Infection
  • Influenza Vaccines
Biological: GSK investigational vaccine GSK2340272A
Two intramuscular injections
  • Experimental: Group A
    Subjects receiving GSK2340272A vaccine according to a 0, 21 days schedule
    Intervention: Biological: GSK investigational vaccine GSK2340272A
  • Experimental: Group B
    Subjects receiving GSK2340272A vaccine according to a 0, 6 months schedule
    Intervention: Biological: GSK investigational vaccine GSK2340272A
Duval X, Caplanusi A, Laurichesse H, Deplanque D, Loulergue P, Vaman T, Launay O, Gillard P. Flexibility of interval between vaccinations with AS03A-adjuvanted influenza A (H1N1) 2009 vaccine in adults aged 18-60 and >60 years: a randomized trial. BMC Infect Dis. 2012 Jul 23;12:162. doi: 10.1186/1471-2334-12-162. PubMed PMID: 22824474; PubMed Central PMCID: PMC3522029.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
312
April 2010
April 2010   (final data collection date for primary outcome measure)

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.
  • Non-childbearing potential is defined as pre-menarche, current tubal ligation, hysterectomy, ovariectomy or post-menopause.
  • 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; a history of 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.
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00975884
113630
Not Provided
Cheri Hudson; Clinical Disclosure Advisor, GSK Clinical Disclosure
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP