Safety and Immunogenicity of A/H1N1v Vaccines in Healthy Adults

NCT ID: NCT00943358

Last Updated: 2012-08-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 175 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2009-12-31

Brief Summary

The purpose of this study is to evaluate the antibody response to one and two doses of influenza A/H1N1v vaccine in healthy adults.

Detailed Description

An observer-blind, single-centre study in which 7 groups of 25-30 male and female adults ≥18-50 years of age will be randomly allocated to receive two doses of cell culture non-adjuvanted or MF59-adjuvanted influenza A/California/4/2009 (H1N1) surface antigen vaccine containing 3.75, 7.5 or 15µg haemagglutinin by intramuscular injection. A second dose of the same vaccine containing the same quantity of antigen as in the first dose will be administered 21 days later. Three additional groups will receive two doses of MF59-adjuvanted influenza A/California/4/2009 (H1N1) surface antigen vaccine containing 7.5 µg haemagglutinin by intramuscular injection on day 0 or separated by 7 or 14 days. Subjects will be observed for local and systemic reactions for 30 minutes after each immunisation and will be monitored for any reactions and other adverse events for 7 days after each immunisation.

Conditions

Influenza

Keywords

influenza; immunogenicity; vaccine

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Vaccine

adjuvanted influenza vaccine

Group Type: ACTIVE_COMPARATOR

MF59 H1N1 vaccine

Intervention Type: BIOLOGICAL

3.75-7.5ug dose

Vaccine 2

non-adjuvanted vaccine

Group Type: ACTIVE_COMPARATOR

Plain H1N1 vaccine

Intervention Type: BIOLOGICAL

7.5-15ug

Interventions

MF59 H1N1 vaccine

3.75-7.5ug dose

Intervention Type: BIOLOGICAL

Plain H1N1 vaccine

7.5-15ug

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Mentally competent adults, who have signed an informed consent form after having received a detailed explanation of the study protocol.

2. Male or female subjects 18-50 years who are either healthy or have a stable medical condition.

3. Able to understand and comply with all study procedures and to complete study diaries

4. Individuals who can be contacted throughout the study and are available for all study visits

5. Females should either be using secure contraceptive precautions including:

• the oral contraceptive pill
• condom/barrier contraception
• partner has had a vasectomy
• be surgically sterilised, or
• post-menopausal (defined as at least two years since the last menstrual period)

Exclusion Criteria

1. Any clinically significant concurrent illness or unstable medical condition including: malignant tumours, autoimmune illnesses (including rheumatoid arthritis), acute or progressive renal or hepatic pathology, chronic obstructive pulmonary disease requiring oxygen therapy, and any active neurological disorder.

2. Individuals with a history of anaphylaxis or serious reactions to vaccines; hypersensitivity to influenzal viral protein, neomycin or polymixin, or products containing mercury.

3. Persons with known immunosuppressive disease or who use systemic immunosuppressive drugs or other drugs listed in section 8 of the British National Formulary (BNF) or chloroquine, gold or penicillamine or other drugs listed in section 10.1.3 of the BNF to suppress a chronic disease process, or have received in the last 6 months radiotherapy or chemotherapy.

4. Subjects who are at high risk of developing illnesses of the immune system.

5. Individuals who are taking immunostimulant therapy or interferon

6. Individuals who have received blood products or immunoglobulins parenterally during the preceding three months.

7. Women should not be pregnant or lactating.

8. Women who refuse to use a reliable contraceptive method throughout the study

9. Known or suspected drug abuse.

10. Individuals who have received another vaccine or investigational medicinal product in the preceding 2 weeks.

11. Unable to lead an independent life either physically or mentally

12. Regularly drink more than 40 units of alcohol weekly

13. Individuals who have had acute respiratory pathology or infections requiring systemic antibiotic or antiviral therapy during the preceding 7 days (chronic antibiotic therapy for prevention of urinary tract infections is acceptable).

14. Individuals who had a temperature >38oC in the preceding 3 days.

15. Individuals who, in the opinion of the investigator, have conditions that might complicate interpretation of the study results.

16. Individuals who have had confirmed pandemic influenza H1 infection

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Public Health England

OTHER_GOV

Sponsor Role: collaborator

Novartis Vaccines

INDUSTRY

Sponsor Role: collaborator

University Hospitals, Leicester

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Iain Stephenson, FRCP

Role: PRINCIPAL_INVESTIGATOR

University Hospitals, Leicester

Locations

University Hospitals Leicester

Leicester, , United Kingdom

Countries

United Kingdom

References

Clark TW, Pareek M, Hoschler K, Dillon H, Nicholson KG, Groth N, Stephenson I. Trial of 2009 influenza A (H1N1) monovalent MF59-adjuvanted vaccine. N Engl J Med. 2009 Dec 17;361(25):2424-35. doi: 10.1056/NEJMoa0907650. Epub 2009 Sep 10.

Reference Type: DERIVED

PMID: 19745215 (View on PubMed)

Other Identifiers

UHL10763

Identifier Type: -

Identifier Source: org_study_id