Clinical Trial of Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector) Against COVID-19

Covid19 Clinical Trial

Official title:

Multicenter, Randomized, Double Blind, Placebo Controlled Parallel Group Study Evaluating Efficacy, Reactogenicity and Safety of Recombinant Vaccine Ad5-nCoV Against Novel Coronavirus Infection in Adult Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04540419
• Other study ID #: Prometheus_Rus
• Status: Completed
• Phase: Phase 3
• Start date: September 11, 2020
• Est. completion date: July 30, 2021

Study information

• Verified date: April 2024
• Source: NPO Petrovax
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a phase III clinical trial to evaluate efficacy, reactogenicity and safety of the vaccine Ad5-nCoV compared with placebo in volunteers at the age from 18 to 85 years，with the randomized, double-blind design

Description:

A total of 500 healthy adult volunteers at the age from 18 to 85 years will be randomized into two treatment (vaccination) groups in ratio 3:1 by double-blind design. Volunteers in group 1 (n=375) will be administered a single dose of the vaccine Ad5-nCoV (5E10vp). Volunteers in group 2 (n=125): will be administered a single dose of placebo. Vaccine Ad5-nCoV or placebo will be administered intramuscularly into the deltoid muscle of the arm at a single dose of 0.5 mL (1 prefilled syringe).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 500
• Est. completion date: July 30, 2021
• Est. primary completion date: June 19, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

1. Presence of signed and dated Informed Consent of volunteer for participation in this study.

2. Men and women at the age of 18-85 years.

3. Bodyweight index 18.5-30.0 kg/m2.

4. The negative result of the test, performed by using PCR, for the presence of SARS-CoV-2 RNA at the stage of screening.

5. Negative result for anti-SARS-CoV-2 IgM and IgG antibodies at the stage of screening.

6. No history of the diagnosis COVID-19.

7. Absence of close contacts with individuals, suspicious for infection SARS-CoV-2, or individuals, in whom the diagnosis COVID-19 was confirmed in laboratory within the last 14 days.

8. Absence of signs of respiratory infection within the last 14 days.

9. Negative results of human immunodeficiency virus (HIV), syphilis, hepatitis B and hepatitis C tests.

10. According to historical data and results of screening examination, a volunteer has no diseases and/or conditions, which in view of Investigator, may influence the safety of volunteer participation and evaluation of study results.

11. Volunteer consent for using safe contraceptive methods through all the study.

Exclusion Criteria:

1. Positive history of allergy, drug intolerance, including increased sensibility to any of components of the test drug product, as well as the history of serious adverse events in the administration of vaccines (such as allergic reactions, respiratory disturbance, angioedema, stomach pain).

2. Axillary body temperature =37.1 °C at the time of screening/randomization.

3. Systolic blood pressure more than 139 mm Hg or less than 100 mm Hg and/or diastolic blood pressure more than 90 mm Hg or less than 60 mm Hg.

4. Clinical significant abnormal laboratory and/or instrumental parameters at screening examination.

5. Acute infectious diseases less than 4 weeks ahead of conduction of screening procedures.

6. Acute and acute course of chronic diseases of GIT, liver, kidneys, cardiovascular, respiratory, nervous and endocrine systems.

7. History of blood and hematopoietic organ diseases.

8. History of diabetes mellitus.

9. History of epilepsy, epileptic syndrome, seizures.

10. History of congenital and acquired immunodeficiency, HIV-infection, lymphoma, leukaemia, systemic lupus erythematosus, juvenile rheumatoid arthritis or other autoimmune diseases.

11. History malignancies.

12. Using immunotropic preparations (immunomodulators, immunostimulators, immunodepressants), antiallergic, cytotoxic preparations for more than 10 sequential days within the last 3 months (except for inhalant and local using glucocorticoids [GCS] or using specified preparations less than 4 weeks ahead of the screening.

13. Using immunoglobulin preparations or blood transfusion less than 3 months ahead of the screening.

14. Using antipyretics (including non-steroidal anti-inflammatory agents and anilides) within 24 hours ahead of randomization.

15. Blood donation or loss (=450 mL of blood or plasma) less than 3 months ahead of the screening.

16. Vaccination within 6 mon. ahead of screening or reluctance to refuse from the administration of any other vaccine during the study.

17. Anamnestic data/data on alcoholism, narcomania, drug abuse, mental illnesses.

18. Major surgery planned within the nearest 6 months or underwent within the last 6 months ahead of the screening.

19. Carrying out of body piercing procedures, an appendix of tattoo less than 1 month ahead of conduction of screening procedures and through all the study.

20. Pregnancy or breast-feeding period.

21. Participation in another clinical study within 3 months ahead of the screening.

22. Psychic, physical and other reasons, not allowing a volunteer to adhere to conditions and procedures of Study Protocol.

23. Volunteers, who are Clinical Site staff.

24. Other reasons, not allowing the volunteer to take part in this study in view of the study physician.

Related Conditions & MeSH terms

• COVID-19
• Covid19

Intervention

Biological:
• Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector)
Intramuscular administration
• Placebo
Intramuscular administration

Locations

Country	Name	City	State
Russian Federation	Municipal budgetary institution "Central City Hospital No. 7"	Ekaterinburg
Russian Federation	Federal budgetary institution of science "Central Research Institute of Epidemiology" of the Federal Service for Surveillance on Consumer Rights Protectionand Human Welfare	Moscow
Russian Federation	Federal State Autonomous Educational Institution of Higher Education "First MoscowState Medical University named after I.M. Sechenov "of the Ministry of Health of the Russian Federation	Moscow
Russian Federation	State Budgetary Institution of Healthcare of the City of Moscow "City Polyclinic No. 2of the Department of Healthcare of the City of Moscow"	Moscow
Russian Federation	Federal State Budgetary Institution "Research Institute of Influenza named after A.A.Smorodintsev "of the Ministry of Health of the Russian Federation	Saint Petersburg
Russian Federation	Limited Liability Company "Research Center Eco-safety"	Saint Petersburg
Russian Federation	Private health care institution "Clinical hospital 'Russian Railways - Medicine' of the city of Yaroslavl"	Yaroslavl

Sponsors (2)

Lead Sponsor	Collaborator
NPO Petrovax	CanSino Biologics Inc.

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Superiority of the vaccine Ad5-nCoV to placebo by the level of seroconversion	Proportion of subjects with four-fold and higher increment of anti-receptor-binding domain antibodies [receptor-binding domain, RBD] of S-protein SARS-CoV-2).	Day 28 after vaccination
Secondary	Immunogenicity of the vaccine Ad5-nCoV compared with placebo (titer of SARS-CoV-2 antibodies)	Geometric mean titer of RBD ? S-protein SARS-CoV-2 antibodies.	Day 14, 28 and after 6 months after vaccination.
Secondary	Immunogenicity of the vaccine Ad5-nCoV compared with placebo (level of seroconversion)	Level of seroconversion (proportion of persons with four-fold and higher increment of RBD ? S-protein SARS-CoV-2 antibodies).	Day 14, 28 and after 6 months after vaccination.
Secondary	Immunogenicity of the vaccine Ad5-nCoV compared with placebo (rise of SARS-CoV-2 antibodies)	Geometric mean fold rise of RBD ? S-protein SARS-CoV-2 antibodies.	Day 14, 28 and after 6 months after vaccination.
Secondary	Immunogenicity of the vaccine Ad5-nCoV compared with placebo (T-cell response)	Quantity of T-cells.	Day 14, 28 and after 6 months after vaccination.
Secondary	Frequency of confirmed COVID-19	Frequency of confirmed COVID-19 (confirmed case of COVID-19: presence of clinical signs and positive result of laboratory test for RNA of virus SARS-CoV-2) (exploratory analysis).	Within 6 months after vaccination (except for COVID-19 cases within 14 days after vaccination)
Secondary	Frequency of confirmed cases of COVID-19, requiring hospitalization	Frequency of confirmed cases of COVID-19, requiring hospitalization. (confirmed case of COVID-19: presence of clinical signs and positive result of laboratory test for RNA of virus SARS-CoV-2) (exploratory analysis).	Within 6 months after vaccination (except for COVID-19 cases within 14 days after vaccination)
Secondary	Frequency of cases with severe course of COVID-19	Frequency of cases with severe course of COVID-19 (confirmed case of COVID-19: presence of clinical signs and positive result of laboratory test for RNA of virus SARS-CoV-2) (exploratory analysis).	Within 6 months after vaccination (except for COVID-19 cases within 14 days after vaccination)
Secondary	Frequency of death due to COVID-19.	Frequency of death due to COVID-19 (exploratory analysis).	Within 6 months after vaccination (except for COVID-19 cases within 14 days after vaccination)
Secondary	Reactogenicity of the vaccine Ad5-nCoV compared with placebo	Frequency and character of general and local postvaccinal reactions.	Day 0 (day of vaccination), Day 2, Day 7
Secondary	Frequency and character of adverse events and serious adverse events.	Frequency and character of adverse events and serious adverse events.	Day 0 - Month 6
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on vital parameters (blood pressure)	Results of evaluation of vital parameters: Systolic blood pressure; Diastolic blood pressure The researcher evaluates each of the vital parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 0, Day 2, Day 7, Day 14, Day 28, Month 6
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on vital parameters (heart rate)	Results of evaluation of vital parameters: • Heart rate. The researcher evaluates each of the vital parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 0, Day 2, Day 7, Day 14, Day 28, Month 6
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on vital parameters (respiratory rate)	Results of evaluation of vital parameters: • Respiratory rate. The researcher evaluates each of the vital parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 0, Day 2, Day 7, Day 14, Day 28, Month 6
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of physical examination	Results of physical examination includes examination of organs and systems: General state Ears, nose, throat Skin and examination of the injection site The lymph nodes The cardiovascular system Respiratory system Nervous system Abdominal organs Kidneys and urinary system Musculoskeletal system.; During the physical examination, the researcher evaluates each of the systems in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 0, Day 2, Day 7, Day 14, Day 28, Month 6
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of electrocardiography (Heart rate)	Results of electrocardiography: • Heart rate (HR) The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of electrocardiography	Results of electrocardiography: Intervals RR, PQ, QT; QRS complex; Corrected QT interval (QTcF). The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of serum chemistry (enzymes)	Results of serum chemistry: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), lactate dehydrogenase (LDH).; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of serum chemistry	Results of serum chemistry: total bilirubin, creatinine, urea, fasting glucose. The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of serum chemistry	Results of serum chemistry: total protein, C-reactive protein. The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of complete blood count (hemoglobin)	Results of complete blood count: hemoglobin The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of complete blood count (hematocrit)	Results of complete blood count: hematocrit.; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of complete blood count (erythrocytes)	Results of complete blood count: erythrocytes.; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of complete blood count	Results of complete blood count: platelets, leukocytes and leukocyte formula (neutrophils, lymphocytes, monocytes, eosinophils, basophils (absolute number).; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of complete blood count (erythrocyte sedimentation rate)	Results of complete blood count: erythrocyte sedimentation rate; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of coagulogram	Results of coagulogram: activated partial thromboplastin time, prothrombin time.; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of coagulogram (fibrinogen)	Results of coagulogram: fibrinogen.; The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of clinical urinalysis (relative density)	Results of clinical urinalysis: relative density. The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of clinical urinalysis (pH)	Results of clinical urinalysis: pH. The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of clinical urinalysis	Results of clinical urinalysis: leukocytes, erythrocytes, cylinders . The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of clinical urinalysis (protein)	Results of clinical urinalysis: protein . The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of clinical urinalysis (glucose)	Results of clinical urinalysis:glucose . The researcher evaluates each of the parameter in the normal / abnormal categories. Clinically significant abnormalities should be reported as adverse events.	Day -7-1 (Screening), Day 2, Day 28
Secondary	To evaluate safety of the vaccine Ad5-nCoV by its effect on results of determination of immunoglobulin E serum concentrations.	Results of determination of immunoglobulin E serum concentrations.	Day -7-1 (Screening), Day 28