Safety and Immunogenicity of a New Inactivated Polio Vaccine in Healthy Adults

• Status: Completed
• Trial end date: 2012-02-01
• Target enrollment: 0
• Participant gender: Male

Summary

The purpose of this trial is to determine whether the new inactivated polio vaccine that is based on attenuated poliovirus strains is safe and to evaluate the immune response in healthy adults.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Pauline Verdijk
• Collaborator: World Health Organization
• Treatments: Vaccines

Criteria

Inclusion Criteria:

• Age 18 to 49, inclusive at the time of enrolment

• in good health as determined by the outcome of medical history, physical examination screening/baseline labs and clinical judgment of the investigator

• Male

• Must have received polio vaccinations with OPV according to the Polish National Immunization Program as a child based on vaccination cards or information given by subjects during interview with investigator

• Preferred: number (and date) of polio vaccinations known

• Willingness and ability to adhere to the study regimen

• Having a signed informed consent form

Exclusion Criteria:

• IPV or OPV booster dose after the age of 12 years

• Positive for HIV, Hepatitis B or Hepatitis C

• Known or suspected allergy against any of the vaccine components

• History of unusual or severe reactions to any previous vaccination

• Known or suspected disease or use of medication that may influence the immune system

• Known or suspected immune deficiency

• Systemic treatment with corticosteroids within one month before screening

• Administration of plasma (including immunoglobulins) or blood products three months prior to the study

• Blood donation within one month before screening

• Any vaccination within three months before screening and during the study until the last visit

• History of any neurological disorder including epilepsy or febrile seizures

• Evidence of excessive alcohol use or drug use

• Any infectious disease at the time of screening and/or inclusion

• Participation in another clinical trial within three months before screening

• Abnormal pre-treatment laboratory parameters which are clinically relevant according to the investigator

• Bleeding disorders or the usage of anticoagulants