drugset / Trial / NCT05762523

Safety and Tolerability Study of the VAC∆6 Vaccine in Volunteers Aged 18-40 Years

NCT05762523

RandomizedParallel-groupOpen-labelPrevention

Summary

The aim of the clinical study is to study the safety and tolerability of the live cell-based vaccine against smallpox and other orthopoxvirus infections (VAC∆6 vaccine) based on vaccinia virus, in intracutaneous administration. The research tasks are to: * evaluate the safety of various schemes for the use of the VAC∆6 vaccine using a set of clinical and laboratory-instrumental methods (thermometry, blood pressure registration, auscultation of the heart and lungs, electrocardiography (ECG), complete blood count and common urine test, biochemical, immunological, and virological studies); * evaluate the reactogenicity of various schemes for the use of the VAC∆6 vaccine (taking into account the number of local and systemic reactions, the percentage of those vaccinated with various degrees of manifestation of systemic and local reactions); * evaluate the possibility of virus shedding into the environment by volunteers; * evaluate the immunological efficacy of various vaccine administration schemes; * identify the development of undesirable reactions to the administration of the vaccine; * evaluate the cellular immune response to the introduction of various schemes for the use of the vaccine; * evaluate preliminary efficacy data in order to select an optimal scheme for the administration of the vaccine to make a decision on conducting Phase II clinical trials in an extended group of volunteers.

Timeline

Start
2019-05-18
Primary completion
2019-07-22
Completion
2020-01-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject OspaVir® Vaccine 0.5 ml Subcutaneous
Subject Smallpox vaccine Vaccine 1e+06 unknown Other
Subject VAC∆6 Vaccine 1e+06 unknown Other
Subject VAC∆6 Vaccine 1e+07 unknown Other