search
Back to results

Immunogenicity, Efficacy and Safety Trial of the Convacell Vaccine in Healthy Volunteers Aged 18 Years and Older

Primary Purpose

COVID-19, Coronavirus Infections, Respiratory Tract Infections

Status
Active
Phase
Phase 2
Locations
Russian Federation
Study Type
Interventional
Intervention
Subunit recombinant vaccine for the prevention of coronavirus infection
Placebo
Sponsored by
St. Petersburg Research Institute of Vaccines and Sera
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COVID-19 focused on measuring COVID-19, cellular immunity, nucleocapsid protein, recombinant vaccine, SPbSRIVS, SARS-CoV-2, Convacell

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Men and women aged 18 Years and Older Written informed consent of the volunteer to participate in the clinical trial (in paper or electronic form) BMI within the range of 18.5 ≤ BWI ≤ 30 kg/m2 with the body weight of not less than 55 kg for men, not less than 45 kg for women and not more than 100 kg for volunteers of both sexes Absence of clinically significant (according to the investigator) deviations from the reference values of clinical, laboratory and instrumental methods of examination at screening Hemodynamic and other vital signs are within normal limits (reference intervals are 60-90 beats/min at rest for HR, up to 22 per minute for RR, body temperature from 35.5 to 36.9 °C; systolic blood pressure (SBP) is considered normal in the range of 100-139 mmHg, diastolic blood pressure (DBP) - in the range of 60-89 mmHg) Volunteers able to fulfill requirements of the Protocol (i.e., fill in the electronic patient's diary, come to follow-up visits) Abstinence from alcohol from the start of screening until completion of Visit 7 procedures (day 42 ± 2) - for stage 2b For fertile women - a negative result of the pregnancy test and consent to observe adequate methods of contraception during the trial and at least two months after vaccination For fertile men - consent to observe adequate methods of contraception during the trial and at least two months after vaccination, except for men after vasectomy with documented azoospermia, and their sexual partners should use methods of contraception that ensure more than 90% reliability or be incapable of conception after a surgical sterilization or have a natural menopause for at least 2 years Throughout the study, the opportunity to use own smartphone with the ability to fill in the electronic patient's diary Exclusion Criteria: History of influenza or acute respiratory viral infection (ARVI) within 2 months before the start of the trial; A serious post-vaccination reaction (temperature above 40 °C, hyperemia or edema more than 8 cm in diameter) or complications (collapse or shock-like condition that developed within 48 hours after vaccination; convulsions accompanied or not accompanied by a fever due to any previous vaccination); Fever, cough, and shortness of breath within 30 days before vaccination; History of COVID-19 within 6 months before screening; The level of IgG antibodies to the SARS-CoV-2 N-protein according to semi-quantitative test (Architect, Abbott) ≥ 3 (positivity rate) at screening; Positive result of the COVID-19 PCR test or antigen COVID-19 test (rapid test); Body temperature ≥ 37,3°C. History of allergies; Any vaccination within 30 days before the screening; History of leukemia, tuberculosis, cancer, autoimmune diseases; History of Quincke's edema; Positive blood test results for HIV, syphilis, hepatitis B/C according to the examination during the screening period (only for Stage IIb) or according to the history (for Stage III). It is acceptable to use the results of previously performed tests, if their prescription does not exceed 60 days before the date of the screening or based on history; Volunteers who received immunoglobulin during the last three months before the trial; History of long-term use (more than 14 days) of immunosuppressants or other immunomodulatory drugs for six months before the trial; Treatment with glucocorticosteroids, including in small doses, as well as local use of drugs containing steroids (> 10 mg of prednisolone or its equivalent for more than 14 days before the screening); History of any confirmed or suspected immunosuppressive or immunodeficiency condition; History of splenectomy; History of chronic diseases of the cardiovascular, bronchopulmonary, neuroendocrine systems, the gastrointestinal tract, liver, kidneys, hematopoietic or immune systems, mental disease in the acute stage or in the decompensation stage (according to history and / or examination on the screening); Transfusion of blood or blood components within 4 months before screening; Any acute infectious diseases during the screening period or past illnesses within 3 months before the screening visit, any chronic infectious diseases in the acute stage during the screening period; Consumption of more than 10 units of alcohol per week or history of alcohol addiction, drug addiction or abuse of pharmaceutical products; Smoking of more than 10 cigarettes per day; Participation in another clinical trial within the last 90 days; Pregnancy or lactation; Coagulopathy, hemophilia, bleeding disorder; Participation in previous clinical trials of the Convacell vaccine, a subunit recombinant vaccine for the prevention of coronavirus infection caused by SARS-CoV-2 virus, or any other vaccines to prevent coronavirus infection caused by the virus SARS-CoV-2 for 6 months before screening; History of anticovid plasma use; Vaccination against COVID-19 within 6 months before screening.

Sites / Locations

  • Limited Liability Company "OLLA-MED"
  • State budgetary health care institution of the city of Moscow "City Clinical Hospital No. 24 of the Department of Health of the City of Moscow"
  • Limited Liability Company "Scientific Research Center Eco-Safety"
  • St. Petersburg State Budgetary Health Institution "City Polyclinic No. 117"
  • Limited Liability Company "Otkrytaya Meditsina"
  • Limited Liability Company "Meditsinskiy Diagnosticheskiy Tsentr"

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Convacell, 1 dose (Stage IIb)

Convacell, 2 doses (Stage IIb)

Convacell, chosen regimen (Stage III)

Placebo, chosen regimen (Stage III)

Arm Description

Participants (230) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, once intramuscularly. A cohort of participants will be allocated (115 participants) for evaluating cell-mediated immunity parameters.

Participants (230) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, twice intramuscularly. A cohort of participants will be allocated (115 participants) for evaluating cell-mediated immunity parameters.

Participants (10 562) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, the regimen chosen in Stage IIb intramuscularly.

Participants (5 282) will be vaccinated Placebo, the regimen chosen in Stage IIb intramuscularly.

Outcomes

Primary Outcome Measures

Change in titer of IgG antibodies to N-protein of SARS-CoV-2 (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Frequency of symptomatic COVID-19 with laboratory-confirmed infection within 6 months after vaccination compared with the placebo group (Stage III)
Laboratory confirmation of SARS-CoV-2 infection in accordance with current clinical guidelines can be a PCR study or an antigen test of a swab from the nasopharynx or oropharynx. The symptomatic form of COVID-19 is the presence of at least one of the following symptoms: fever/chills, cough, shortness of breath or difficulty breathing, fatigue, muscle or body pain, headache, loss of the sense of taste or smell, sore throat, nasal congestion or runny nose, nausea or vomiting, diarrhea. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.

Secondary Outcome Measures

Change in titer of IgM antibodies to N-protein of SARS-CoV-2 on day 42 after initial vaccination (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Proportion of SARS-CoV-2 seropositive participants on day 42 after initial vaccination (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Change in titer of IgG antibodies to N-protein of SARS-CoV-2 on day 42 after initial vaccination (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of seroconversion (appearance of specific antibodies to SARS-CoV-2 N-protein) on day 42 after initial vaccination (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Change from Baseline in the Mean Specifically Sensitized T-lymphocytes (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Number of volunteers hospitalized with COVID-19 (Stage IIb)
Total number of SARS-CoV-2 infection cases (laboratory-confirmed) Total number of COVID-19 cases (laboratory-confirmed) Total number of COVID-19 related deaths Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Frequency of laboratory confirmed asymptomatic SARS-CoV-2 infections within 6 months. after initial vaccination compared with the placebo group (Stage III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Frequency of laboratory-confirmed severe COVID-19 (Stage III)
Frequency of laboratory-confirmed severe COVID-19 in accordance with current criteria RR > 30/min Blood oxygen saturation (SpO2) ≤ 93% Oxygenation index (PaO2 /FiO2) ≤ 300 mmHg Decreased level of consciousness, agitation Unstable hemodynamics (systolic arterial pressure [SBP] less than 90 mm Hg. or diastolic blood pressure [DBP] less than 60 mmHg, diuresis less than 20 ml/hour) Lung changes on computed tomography (CT) or radiographs typical for a viral lesion Arterial blood lactate > 2 mmol/l Assessment on a quick scale (quick Sequential Organ Failure Assessment, qSOFA) > 2 points Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Overall frequency of all AEs/SAEs (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Overall frequency of all AEs/SAEs associated with the study drug (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of local post-vaccination reactions at the injection site (Stage IIb and III)
Erythema at the injection site (presence/absence); Soreness (presence/absence), including assessment duration of preservation of pain and its intensity: weak, moderate, strong; Edema (presence/absence), including diameter infiltrate assessment: weak (up to 2.5 cm), medium (from 2.6 to 5 cm), strong (more than 5 cm or the presence of lymphangitis) reactions; Enlargement of regional lymph nodes (presence/absence); Induration at the injection site (presence/absence); Itching at the injection site (presence/absence). Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of systemic post-vaccination reactions at the injection site (Stage IIb and III)
Increase in body temperature, including an assessment fever severity: mild (37.3-37.5°C), moderate (37.6-38.5°С) and strong (> 38.5°С); Chills; Deterioration of general health, malaise; Headache; Dizziness; Loss of appetite; Insomnia; Nausea, Vomiting, Dyspepsia; Diarrhea; Body pain or muscle weakness; Sweating; Pain in the joints; Pain in the abdomen; Convulsions; Myalgia; Enlargement of regional lymph nodes. Changes in the side of the mucous membranes, the presence of papules, vesicles, erosions. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of local post-vaccination reactions at the injection site (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Frequency of systemic post-vaccination reactions (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of toxic post-vaccination complications (Stage IIb and III)
Septic conditions, generalized infection. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of allergic post-vaccination complications (Stage IIb and III)
Polymorphous eruption, angioedema, arthralgia, anaphylactic shock. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The frequency of neurological post-vaccination complications (Stage IIb and III)
Encephalitis, neuritis, polyneuritis. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The presence of allergic reactions (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Сhange in white blood cell count and relative white blood cell count (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Сhange in neutrophils count and relative neutrophils count (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Сhange in lymphocytes count and relative lymphocytes count (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Сhange in monocyte count and relative monocyte count (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Сhange in the IgE level (Stage IIb)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
The proportion of participants with delayed post-vaccination reactions (percent) (Stage IIb and III)
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.

Full Information

First Posted
January 17, 2023
Last Updated
August 29, 2023
Sponsor
St. Petersburg Research Institute of Vaccines and Sera
search

1. Study Identification

Unique Protocol Identification Number
NCT05726084
Brief Title
Immunogenicity, Efficacy and Safety Trial of the Convacell Vaccine in Healthy Volunteers Aged 18 Years and Older
Official Title
Multicentre, Double-blind, Randomized, Prospective, Placebo-controlled Trial to Assess the Immunogenicity, Efficacy and Safety of the Coronavirus Vaccine in Healthy Volunteers Aged 18 Years and Older
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 24, 2022 (Actual)
Primary Completion Date
October 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Petersburg Research Institute of Vaccines and Sera

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this clinical trial is to assess the immunogenicity, efficacy and safety of the Convacell vaccine in healthy adult volunteers aged 18 years and older. The main questions it aims to answer are: To assess the immunogenicity and safety of single and double dose intramuscular administration of the Convacell vaccine; To assess the epidemiological effectiveness of the Convacell vaccine in the prevention of SARS-CoV-2 infection and development of severe COVID-19 compared with placebo when single or double intramuscular injection.
Detailed Description
The trial will be conducted in two stages (Stage IIb and Stage III). • Stage IIb Participants will be vaccinated one dose or two doses of the Convacell vaccine. Investigators will compare one dose and two doses groups and will choose the best vaccine dosage regimen in terms of immunogenicity and safety. • Stage III Participants will be vaccinated the Convacell vaccine or Placebo. Investigators will use the dosage regimen chosen in IIb stage.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19, Coronavirus Infections, Respiratory Tract Infections, COVID-19 Respiratory Infection
Keywords
COVID-19, cellular immunity, nucleocapsid protein, recombinant vaccine, SPbSRIVS, SARS-CoV-2, Convacell

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
16304 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Convacell, 1 dose (Stage IIb)
Arm Type
Experimental
Arm Description
Participants (230) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, once intramuscularly. A cohort of participants will be allocated (115 participants) for evaluating cell-mediated immunity parameters.
Arm Title
Convacell, 2 doses (Stage IIb)
Arm Type
Experimental
Arm Description
Participants (230) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, twice intramuscularly. A cohort of participants will be allocated (115 participants) for evaluating cell-mediated immunity parameters.
Arm Title
Convacell, chosen regimen (Stage III)
Arm Type
Experimental
Arm Description
Participants (10 562) will be vaccinated Convacell Vaccine, recombinant subunit vaccine for prevention of coronavirus infection, the regimen chosen in Stage IIb intramuscularly.
Arm Title
Placebo, chosen regimen (Stage III)
Arm Type
Placebo Comparator
Arm Description
Participants (5 282) will be vaccinated Placebo, the regimen chosen in Stage IIb intramuscularly.
Intervention Type
Biological
Intervention Name(s)
Subunit recombinant vaccine for the prevention of coronavirus infection
Other Intervention Name(s)
Convacell
Intervention Description
solution for intramuscular injection, 0.5 ml
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
solution for intramuscular injection, 0.5 ml
Primary Outcome Measure Information:
Title
Change in titer of IgG antibodies to N-protein of SARS-CoV-2 (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
Frequency of symptomatic COVID-19 with laboratory-confirmed infection within 6 months after vaccination compared with the placebo group (Stage III)
Description
Laboratory confirmation of SARS-CoV-2 infection in accordance with current clinical guidelines can be a PCR study or an antigen test of a swab from the nasopharynx or oropharynx. The symptomatic form of COVID-19 is the presence of at least one of the following symptoms: fever/chills, cough, shortness of breath or difficulty breathing, fatigue, muscle or body pain, headache, loss of the sense of taste or smell, sore throat, nasal congestion or runny nose, nausea or vomiting, diarrhea. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-180 (6 months)
Secondary Outcome Measure Information:
Title
Change in titer of IgM antibodies to N-protein of SARS-CoV-2 on day 42 after initial vaccination (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
Proportion of SARS-CoV-2 seropositive participants on day 42 after initial vaccination (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
Change in titer of IgG antibodies to N-protein of SARS-CoV-2 on day 42 after initial vaccination (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
The frequency of seroconversion (appearance of specific antibodies to SARS-CoV-2 N-protein) on day 42 after initial vaccination (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
Change from Baseline in the Mean Specifically Sensitized T-lymphocytes (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0, 42
Title
Number of volunteers hospitalized with COVID-19 (Stage IIb)
Description
Total number of SARS-CoV-2 infection cases (laboratory-confirmed) Total number of COVID-19 cases (laboratory-confirmed) Total number of COVID-19 related deaths Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb; Days 0-49
Title
Frequency of laboratory confirmed asymptomatic SARS-CoV-2 infections within 6 months. after initial vaccination compared with the placebo group (Stage III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-180 (6 months)
Title
Frequency of laboratory-confirmed severe COVID-19 (Stage III)
Description
Frequency of laboratory-confirmed severe COVID-19 in accordance with current criteria RR > 30/min Blood oxygen saturation (SpO2) ≤ 93% Oxygenation index (PaO2 /FiO2) ≤ 300 mmHg Decreased level of consciousness, agitation Unstable hemodynamics (systolic arterial pressure [SBP] less than 90 mm Hg. or diastolic blood pressure [DBP] less than 60 mmHg, diuresis less than 20 ml/hour) Lung changes on computed tomography (CT) or radiographs typical for a viral lesion Arterial blood lactate > 2 mmol/l Assessment on a quick scale (quick Sequential Organ Failure Assessment, qSOFA) > 2 points Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-180 (6 months)
Title
Overall frequency of all AEs/SAEs (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
Overall frequency of all AEs/SAEs associated with the study drug (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
The frequency of local post-vaccination reactions at the injection site (Stage IIb and III)
Description
Erythema at the injection site (presence/absence); Soreness (presence/absence), including assessment duration of preservation of pain and its intensity: weak, moderate, strong; Edema (presence/absence), including diameter infiltrate assessment: weak (up to 2.5 cm), medium (from 2.6 to 5 cm), strong (more than 5 cm or the presence of lymphangitis) reactions; Enlargement of regional lymph nodes (presence/absence); Induration at the injection site (presence/absence); Itching at the injection site (presence/absence). Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-7 after initial vaccination and revaccination
Title
The frequency of systemic post-vaccination reactions at the injection site (Stage IIb and III)
Description
Increase in body temperature, including an assessment fever severity: mild (37.3-37.5°C), moderate (37.6-38.5°С) and strong (> 38.5°С); Chills; Deterioration of general health, malaise; Headache; Dizziness; Loss of appetite; Insomnia; Nausea, Vomiting, Dyspepsia; Diarrhea; Body pain or muscle weakness; Sweating; Pain in the joints; Pain in the abdomen; Convulsions; Myalgia; Enlargement of regional lymph nodes. Changes in the side of the mucous membranes, the presence of papules, vesicles, erosions. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-7 after initial vaccination and revaccination
Title
The frequency of local post-vaccination reactions at the injection site (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-21 after initial vaccination and revaccination
Title
Frequency of systemic post-vaccination reactions (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Days 0-42 after initial vaccination
Title
The frequency of toxic post-vaccination complications (Stage IIb and III)
Description
Septic conditions, generalized infection. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
The frequency of allergic post-vaccination complications (Stage IIb and III)
Description
Polymorphous eruption, angioedema, arthralgia, anaphylactic shock. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
The frequency of neurological post-vaccination complications (Stage IIb and III)
Description
Encephalitis, neuritis, polyneuritis. Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
The presence of allergic reactions (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)
Title
Сhange in white blood cell count and relative white blood cell count (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Day 0 (screening), day 28 ± 2 (visit 4)
Title
Сhange in neutrophils count and relative neutrophils count (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Day 0 (screening), day 28 ± 2 (visit 4)
Title
Сhange in lymphocytes count and relative lymphocytes count (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Day 0 (screening), day 28 ± 2 (visit 4)
Title
Сhange in monocyte count and relative monocyte count (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Day 0 (screening), day 28 ± 2 (visit 4)
Title
Сhange in the IgE level (Stage IIb)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
Day 0 (screening), day 28 ± 2 (visit 4)
Title
The proportion of participants with delayed post-vaccination reactions (percent) (Stage IIb and III)
Description
Outcome Measure is analyzed separately in the 18-60 and >60 age subgroups.
Time Frame
through trial Stage IIb (Days 0-49), through trial Stage III (Days 0-196)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men and women aged 18 Years and Older Written informed consent of the volunteer to participate in the clinical trial (in paper or electronic form) BMI within the range of 18.5 ≤ BWI ≤ 30 kg/m2 with the body weight of not less than 55 kg for men, not less than 45 kg for women and not more than 100 kg for volunteers of both sexes Absence of clinically significant (according to the investigator) deviations from the reference values of clinical, laboratory and instrumental methods of examination at screening Hemodynamic and other vital signs are within normal limits (reference intervals are 60-90 beats/min at rest for HR, up to 22 per minute for RR, body temperature from 35.5 to 36.9 °C; systolic blood pressure (SBP) is considered normal in the range of 100-139 mmHg, diastolic blood pressure (DBP) - in the range of 60-89 mmHg) Volunteers able to fulfill requirements of the Protocol (i.e., fill in the electronic patient's diary, come to follow-up visits) Abstinence from alcohol from the start of screening until completion of Visit 7 procedures (day 42 ± 2) - for stage 2b For fertile women - a negative result of the pregnancy test and consent to observe adequate methods of contraception during the trial and at least two months after vaccination For fertile men - consent to observe adequate methods of contraception during the trial and at least two months after vaccination, except for men after vasectomy with documented azoospermia, and their sexual partners should use methods of contraception that ensure more than 90% reliability or be incapable of conception after a surgical sterilization or have a natural menopause for at least 2 years Throughout the study, the opportunity to use own smartphone with the ability to fill in the electronic patient's diary Exclusion Criteria: History of influenza or acute respiratory viral infection (ARVI) within 2 months before the start of the trial; A serious post-vaccination reaction (temperature above 40 °C, hyperemia or edema more than 8 cm in diameter) or complications (collapse or shock-like condition that developed within 48 hours after vaccination; convulsions accompanied or not accompanied by a fever due to any previous vaccination); Fever, cough, and shortness of breath within 30 days before vaccination; History of COVID-19 within 6 months before screening; The level of IgG antibodies to the SARS-CoV-2 N-protein according to semi-quantitative test (Architect, Abbott) ≥ 3 (positivity rate) at screening; Positive result of the COVID-19 PCR test or antigen COVID-19 test (rapid test); Body temperature ≥ 37,3°C. History of allergies; Any vaccination within 30 days before the screening; History of leukemia, tuberculosis, cancer, autoimmune diseases; History of Quincke's edema; Positive blood test results for HIV, syphilis, hepatitis B/C according to the examination during the screening period (only for Stage IIb) or according to the history (for Stage III). It is acceptable to use the results of previously performed tests, if their prescription does not exceed 60 days before the date of the screening or based on history; Volunteers who received immunoglobulin during the last three months before the trial; History of long-term use (more than 14 days) of immunosuppressants or other immunomodulatory drugs for six months before the trial; Treatment with glucocorticosteroids, including in small doses, as well as local use of drugs containing steroids (> 10 mg of prednisolone or its equivalent for more than 14 days before the screening); History of any confirmed or suspected immunosuppressive or immunodeficiency condition; History of splenectomy; History of chronic diseases of the cardiovascular, bronchopulmonary, neuroendocrine systems, the gastrointestinal tract, liver, kidneys, hematopoietic or immune systems, mental disease in the acute stage or in the decompensation stage (according to history and / or examination on the screening); Transfusion of blood or blood components within 4 months before screening; Any acute infectious diseases during the screening period or past illnesses within 3 months before the screening visit, any chronic infectious diseases in the acute stage during the screening period; Consumption of more than 10 units of alcohol per week or history of alcohol addiction, drug addiction or abuse of pharmaceutical products; Smoking of more than 10 cigarettes per day; Participation in another clinical trial within the last 90 days; Pregnancy or lactation; Coagulopathy, hemophilia, bleeding disorder; Participation in previous clinical trials of the Convacell vaccine, a subunit recombinant vaccine for the prevention of coronavirus infection caused by SARS-CoV-2 virus, or any other vaccines to prevent coronavirus infection caused by the virus SARS-CoV-2 for 6 months before screening; History of anticovid plasma use; Vaccination against COVID-19 within 6 months before screening.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ellina Ruzanova
Organizational Affiliation
St. Petersburg Research Institute of Vaccines and Sera
Official's Role
Study Director
Facility Information:
Facility Name
Limited Liability Company "OLLA-MED"
City
Moscow
Country
Russian Federation
Facility Name
State budgetary health care institution of the city of Moscow "City Clinical Hospital No. 24 of the Department of Health of the City of Moscow"
City
Moscow
Country
Russian Federation
Facility Name
Limited Liability Company "Scientific Research Center Eco-Safety"
City
Saint Petersburg
Country
Russian Federation
Facility Name
St. Petersburg State Budgetary Health Institution "City Polyclinic No. 117"
City
Saint Petersburg
Country
Russian Federation
Facility Name
Limited Liability Company "Otkrytaya Meditsina"
City
Tol'yatti
Country
Russian Federation
Facility Name
Limited Liability Company "Meditsinskiy Diagnosticheskiy Tsentr"
City
Yaroslavl
Country
Russian Federation

12. IPD Sharing Statement

Learn more about this trial

Immunogenicity, Efficacy and Safety Trial of the Convacell Vaccine in Healthy Volunteers Aged 18 Years and Older

We'll reach out to this number within 24 hrs