Clinical trial

Randomized Controlled Trial to Compare the Immunogenicity of Intramuscular Versus Intradermal Trivalent Inactivated Split Virion Influenza Vaccine in HIV-infected Men Who Have Sex With Men in Bangkok, Thailand

Name
CDC-NCIRD-6181
Description
This study will assess the efficacy of a new intradermal formulation of the trivalent inactivated influenza vaccine compared to the standard intramuscular vaccine in HIV-infected men who have sex with men in Bangkok, Thailand. Relative efficacy of the two different formulations of influenza vaccine will be assessed by comparing immunologic responses to vaccine between the two study arms.
Trial arms
Trial start
2011-11-01
Estimated PCD
2013-09-09
Trial end
2015-10-01
Status
Completed
Phase
Early phase I
Treatment
Intradermal vaccine
15ug
Arms:
HIV+, CD4<200, ID vaccine, HIV+, CD4>=200, ID vaccine, HIV-, ID vaccine
Intramuscular vaccine
15ug
Arms:
HIV+, CD4 >=200, IM vaccine, HIV+, CD4<200, IM vaccine, HIV-, IM vaccine
Size
415
Primary endpoint
Antibody titers
30 days
Eligibility criteria
Inclusion Criteria: * Thai men by nationality who have sex with men * HIV-infected or HIV-uninfected men * At least 18 years of age * Willing and able to provide written informed consent * Availability and commitment for 12 months of study follow-up (3 study visits) Exclusion Criteria: * Men with severe allergies to chicken eggs (they will specifically be asked about severe egg allergies during the screening visit; appendix C1) * Men \> 60 years of age * Men who have had a severe reaction to influenza vaccine in the past * Men with a history of Guillain-Barré Syndrome * Men who received influenza vaccine within 12 months prior to enrollment * Men who are on steroid therapy or other immunosuppressant medications * Men who received any vaccine in the 4 weeks prior to the first study visit or who plan to receive a vaccine (other than influenza vaccine provided through the study protocol) in the 4 weeks following the first study visit * Men who received an experimental agent (vaccine, drug, biologic, device, blood product, medication) within 1 month prior to enrollment in this study, or expect to receive an experimental agent during the 12 month study period * Men who have any condition, in the opinion of the investigator, that would place them at an unacceptable risk of injury or render them unable to meet requirements of the protocol. (e.g., severe reaction to another vaccine, blood clotting disorder, inflammatory skin condition). * Foreign (non-Thai) nationality
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 415, 'type': 'ACTUAL'}}
Updated at
2024-06-05

1 organization

2 products

1 indication

Indication
Influenza