Preventive Immunization COVID-19
Conditions
Keywords
COVID-19, SARS-CoV-2, vector vaccine
Brief summary
The purpose of the study is to assess safety, tolerability and immunogenicity of the drug Gam-COVID-Vac , a solution for intramuscular administration, with the participation of healthy volunteers Study objectives A safety and tolerability assessment of the drug Gam-COVID-Vac , solution for intramuscular administration, using single dose of each component (Stage 1). A safety and tolerability assessment of the drug Gam-COVID-Vac , solution for intramuscular administration, using prime-boost immunization according to the proposed scheme (Stage 2). Post-vaccination immunity assessment at different time points after vaccination by: * Determination of antigen-specific antibody titer in blood serum by ELISA by comparison with baseline values before the vaccine administration and at days 14, 21, 28, and 42 after vaccination (hereinafter, the countdown comes from the first time of the vaccine administration); * Determination of virus neutralizing antibody titer before and at days 14, 28, and 42 after vaccination; * Determination of antigen-specific cellular immunity (specific T-cell immunity) before the vaccine administration and at days 14 and 28 after vaccination.
Detailed description
An open two stage non-randomized Phase 1 study with the participation of healthy volunteers. This clinical trial is an open study of safety, tolerability and immunogenicity of the drug Gam-COVID-Vac , ly solution for intramuscular administration, with the participation of healthy volunteers. Stage one 1. the First group, 9 volunteers, will receive the drug, a solution for intramuscular administration, in the mode of single immunization with component 1 in a full therapeutic dose. 2. the Second group, 9 volunteers, will receive the drug, a solution for intramuscular administration, in the mode of single immunization with component 2 in the full therapeutic dose. The studied drugs will be administered to a total of 18 volunteers in a hospital setting and after administration, the drug's safety will be continuously monitored for 5 days. Based on the results of the safety assessment, the Chief investigator decides to proceed to the second stage of the study on the 5th day after the introduction of the studied drugs. Second stage The second stage will include 20 volunteers and three understudies. Volunteers of the second stage will be vaccinated no earlier than 5 days after vaccination of participants of the first stage. Volunteers participating in the second stage of the study (a total of 20 people) will receive the study drug according to the booster scheme: the introduction of component 1 will be carried out on day 1, and component 2-on the 21st day of the study. Follow-up will be carried out during 4 visits: on 7, 14, 28, 42 days after administration of the drug, and phone calls at days 90 and 180 Throughout the inpatient observation and the follow-up period of visits during the entire study, safety information will be collected
Interventions
BIOLOGICALGam-COVID-Vac
adenoviral-based vaccine against SARS-CoV-2
Sponsors
Acellena Contract Drug Research and Development
Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
An open, prospective, two-stage, non-randomized, first-phase study involving healthy volunteers
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
1. males and females within the age range from 18 to 60 years; 2. written informed consent; 3. subject body mass index (BMI): 18.5 ≤ BMI ≤ 30; 4. negative PCR test results for SARS-CoV-2 (during the screening); 5. no history of COVID-2019 disease; 6. no contacts of volunteers with patients with COVID-2019 for at least 14 days; 7. negative test results for IgM and IgG antibodies to SARS-CoV-2; 8. subject agrees to use effective contraceptive methods during the entire period of participation in the study; 9. absence of acute infectious diseases at the time of vaccine administration and 14 days before vaccination; 10. negative pregnancy test of blood or urine (for women of childbearing age); 11. subject has negative tests for HIV, hepatitis B and С, syphilis or confirmed medical history; 12. subject has a negative result of the urine test for residual narcotic drugs; 13. negative test for alcohol in exhaled air; 14. the absence of malignant diseases of any nature and localization; 15. in medical history and based on the screening results, subject has no diseases or pathologies of the gastrointestinal system, liver, kidneys, cardiovascular system and blood, CNS, musculoskeletal system, urogenital, immune and endocrine systems that from the point of view of the researcher and/or of the organizer of the study, may affect the safety of the volunteer and the evaluation of the study results (clinical, instrumental and laboratory tests did not reveal diseases or clinically significant deviations).
Exclusion criteria
1. volunteer involvement in another study over the last 90 days; 2. any vaccination over the last 30 days; 3. history of COVID-2019 disease; 4. positive PCR test results for SARS-CoV-2 (during the screening); 5. positive test results for IgM and IgG antibodies to SARS-CoV-2; 6. health staff in contact with people with COVID-2019; 7. respiratory symptoms in the last 14 days; 8. the administration of immunoglobulins or other blood products in the last 3 months; 9. regular current or past use of narcotic drugs; 10. subject has received immunosuppressive and/or immunomodulating agents within 6 months before the start of the study; 11. pregnancy or breast feeding; 12. exacerbation of allergic diseases at the time of vaccination; 13. subject has systolic blood pressure less than 100 mm Hg or greater than 139 mm Hg; diastolic blood pressure less than 60 mm Hg or greater than 90 mm Hg; heart rate lower than 60 beats per minute or above 100 beats per minute; 14. a burdened allergic history (anaphylactic shock, Quincke's edema, polymorphic exudative eczema, atopy, a history of serum sickness, hypersensitivity or allergic reactions to the introduction of any vaccines in history, known allergic reactions to vaccine components, etc.); 15. a history of autoimmune diseases in the volunteer's medical history and in relatives' medical history of the 1-2 degree of kinship; 16. subject smokes more than 10 cigarettes per day; 17. alcohol intake exceeding the low-risk level: no more than 20 grams of pure alcohol per day, no more than 5 days a week, alcohol intake within 48 hours before the administration of the drug; 18. planned hospitalization and/or surgery during the period of participation in the study, as well as 4 weeks before the expected date of the administration of the drug; 19. the presence of an associated disease that may affect the assessment of the results of the study; 20. any conditions that, according to the researcher's doctor, may be a contraindication to the participation in the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changing ofantibody levels against the SARS-CoV-2 glycoprotein S in 42 days | at days 0,14, 21, 28, 42 | Determination of antibody levels against the SARS-CoV-2 glycoprotein S measured by an ELISA vs. baseline values |
| Number of Participants With Adverse Events | through the whole study, an average of 180 days | Determination of Number of Participants With Adverse Events |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changing of of virus neutralizing antibody titer | at days 0,14, 28, 42 | Determination of virus neutralizing antibody titer |
| Changing of antigen-specific cellular immunity level | at days 0,14, 42 | Determination of antigen-specific cellular immunity (specific T-cell immunityin particular, IFN-gamma production or lymphoproliferation) |
Countries
Russia
Outcome results
None listed