NCT03255278

Evaluation of the Safety and Immunogenicity of the Recombinant Subunit Vaccine "GamTBvac" Against the Tuberculosis.

Evaluation of the Safety and Immunogenicity of the Recombinant Subunit Vaccine "GamTBvac" Against the Tuberculosis. Comparative Placebo-controlled Study With a Two-fold Increase of the Vaccine Dose in Healthy Volunteers Aged 18-49 Years.

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 60 (actual)
• Sponsor: Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation · Academic / Other
• Sex: All
• Age: 18 Years – 49 Years
• Healthy volunteers: Accepted

Summary

The study is aimed to evaluate the safety and immunogenicity of the medicinal product "GamTBvac" - a recombinant subunit vaccine against the tuberculosis. The study is designed as a comparative placebo-controlled study with a two-fold increase of an applied dose among healthy volunteers aged 18-49 years.

Detailed description

The clinical trial study of the "GamTBvac" vaccine against the tuberculosis is a comparative placebo-controlled study with a two-fold increase of an applied dose among healthy volunteers aged 18-49 years. The product "GamTBvac" is a lyophilized substance consisted of the purified recombinant subunit antigens of Mycobacterium tuberculosis, that is applied for the preparing of the solution for a subcutaneous administration. Currently the study is at the first phase. The aims of the study are: a) to confirm the safety of the product in the healthy volunteers; b) to select the optimal administration dose; c) to evaluate of the immunogenicity of the vaccine; d) to investigate the immune cell memory as a response to the vaccination. The total number of the volunteers in the study is 60: 1. at the first stage to estimate the safety and portable of the vaccine, two groups of volunteers each includes 12 persons got the single decreased dose (0.25 of the planned dose for regular administration) of the vaccine (the first group, 12 persons), and the 0.5 ml of the placebo (the second group, 12 persons); 2. at the second stage to select the optimal dose and the scheme of the vaccine administration, additionally three groups, each consist of 12 persons of volunteers will be recruited. The first group will get double vaccination of a decreased dose (0.25 of the regular dose), the second group will get the double vaccination of a mean dose (0.5 of the regular dose), and the third one will get the double vaccination of the maximum (1.0 regular) dose. The inclusion criteria for the volunteers of the study are: healthy males either females aged 18-49 years who have previously got the BCG vaccine. The exclusion criterion is the presence of the latent tuberculosis in the patient that is confirmed during the preliminary laboratory screening.

Conditions

• Tuberculosis

Interventions

Type	Name	Description
BIOLOGICAL	Single GamTBvac vaccination (0.25 dose)	Single administration of the decreased dose of vaccine (0.25 of regular dose) to evaluate the safety.
BIOLOGICAL	Placebo administration	Single administration of the placebo (0.5 ml) to a placebo safety study group (Arm 2).
BIOLOGICAL	Double GamTBvac vaccination (0.25 dose)	Double sequential administration of the decreased dose of vaccine (0.25 of regular dose) to evaluate the immunogenicity.
BIOLOGICAL	Double GamTBvac vaccination (0.5 dose)	Double sequential administration of the mean dose of vaccine (0.5 of regular dose) to evaluate the immunogenicity.
BIOLOGICAL	Double GamTBvac vaccination (1.0 dose)	Double sequential administration of the regular dose of vaccine to evaluate the immunogenicity.

Timeline

• Start date: 2017-01-15
• Primary completion: 2017-12-13
• Completion: 2017-12-13
• First posted: 2017-08-21
• Last updated: 2017-12-27

Locations

1 site across 1 country: Russia