Efficacy, Safety and Immunogenicity Study of the Recombinant Two-component COVID-19 Vaccine (CHO Cell)(Recov)

COVID-19 Clinical Trial

Official title:

A Multicenter, Randomized, Double-blinded, Placebo-controlled Phase III Trial to Evaluate the Efficacy, Safety and Immunogenicity of the Recombinant Two-component COVID-19 Vaccine (CHO Cell) in Adults Aged 18 Years and Older

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05398848
• Other study ID #: REC611C303
• Status: Completed
• Phase: Phase 3
• Start date: October 31, 2022
• Est. completion date: December 29, 2023

Study information

• Verified date: February 2024
• Source: Jiangsu Rec-Biotechnology Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter designed Phase III clinical trial. About 10000 participants plan to be enrolled.The objectives of this study are to evaluate the efficacy, safety and immunogenicity of the recombinant two-component COVID-19 vaccine (CHO cell) in adults

Description:

This study is a multicenter, randomized, double-blinded, placebo-controlled Phase III clinical trial. The objectives are to evaluate the efficacy, safety, and immunogenicity of ReCOV in adults aged 18 years and older who have not received any COVID-19 vaccination, and have no history of known COVID-19 in previous 6 months. Three-dose intramuscular (IM) vaccination schedule (21 days interval) will be applied. About 10000 participants (about 15% participants ≥ 60 years old) with SARS-CoV-2 antibody (IgM and IgG) negative at baseline, will be randomized in a ratio of 1:1 to receive ReCOV (20 μg) or placebo on Day 0, Day 21, and Day 42, respectively. Participants will be stratified by age (18-59 years, ≥ 60 years) and study sites (if applicable). For efficacy visits, study staff will contact participants on a weekly basis to remind reporting any signs or symptoms of COVID-19. If participants report any signs or symptoms that may be related to COVID-19, they will be required to immediately conduct an unscheduled visit under the instruction by site staff for COVID-19 related assessment and receiving treatment as deemed appropriate. For reactogenicity and safety visits, all vaccinated participants will be observed for 30 minutes after each dose vaccination at study site for solicited or unsolicited AEs, and will be given subject diary to record solicited AEs within 7 days after each vaccination, and unsolicited AEs from the 1st vaccination to 28 days after the 3rd vaccination. Approximately 600 participants will be included in the immunogenicity subgroup. Except for the efficacy and safety follow-up visits described above, this subgroup will be collected blood sample on Day 0 (pre-vaccination) and 14 days (+3 days), 90 days (±15 days) and 6 months (±15 days) after the 3rd dose.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7623
• Est. completion date: December 29, 2023
• Est. primary completion date: September 4, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Aged 18 years and older.

2. Able and willing to comply with all study requirements.

3. Willing to allow investigators to discuss the medical history with his/her general practitioner/personal doctors and access all medical records which are relevant to study procedures.

4. Healthy adults, or adults with stable medical condition who have a pre-existing medical condition that does not meet any exclusion criteria. A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization for worsening disease during the 3 months before enrollment.

5. For females of childbearing potential only, willing to practice continuous effective contraception until 90 days after the final dose vaccination, and have negative pregnancy tests before each dose vaccination.

• Nonchildbearing potential is defined as surgically sterile (history of bilateral tubal ligation, bilateral oophorectomy, hysterectomy) or postmenopausal. A follicle-stimulating hormone (FSH) level and the amenorrhea duration (e.g. amenorrhea for = 12 consecutive months prior to screening without an alternative medical cause) may be measured at the discretion of investigator to confirm postmenopausal status.
• The effective contraceptive methods include sexual abstinence or adequate contraceptive measures such as intrauterine or implanted contraceptive device, oral contraceptives, injected or implanted contraceptives, sustained-release topical contraceptives, condoms (male), diaphragm, and cervical cap, etc.

6. Males participating in this study who are involved in heterosexual sexual activity must agree to practice adequate contraception (as described above) and refrain from donating sperm until 90 days after receiving the final dose vaccination.

7. Agreement to refrain from blood donation during the study.

8. Provide written informed consent form (ICF) prior to study enrollment.

Exclusion Criteria:

1. Laboratory confirmed SARS-CoV-2 infection defined by RT-PCR assay at screening. Participants with negative result for rapid antigen testing can be enrolled before having the result of RT-PCR assay, however, the participant needs to be withdrawn the following vaccination if the RT-PCR result shows positive.

2. SARS-CoV-2 antibodies (IgM or IgG) positive at screening.

3. Medical history of severe acute respiratory syndrome (SARS), middle east respiratory syndrome (MERS) and COVID-19 within 6 months prior to the randomization.

4. Fever (oral temperature = 37.5°C / axillary temperature = 37.3°C) on the day of vaccination or within recent 72 hours.

5. History of severe allergic disease or reactions likely to be exacerbated by any component of ReCOV, such as allergic shock, allergic laryngeal edema, allergic purpura, thrombocytopaenic purpura, local hypersensitive necrosis reaction (Arthus reaction), or prior history of serious adverse reaction to any vaccine or drug, such as allergy, urticaria eczema, dyspnea, and angioneurotic edema.

6. Have malignant tumor (except for skin basal cell carcinoma or carcinoma uterine cervix in situ) and immune disease (e.g., documented human immunodeficiency virus [HIV] infection, systemic lupus erythematosus, rheumatoid arthritis, asplenia or splenectomy, and other immune disease that may influence immune response at investigator's discretion).

7. Have other severe and/or uncontrolled conditions, including but not limited to, acute infectious disease, cardiovascular disease, respiratory disease, gastrointestinal disease, liver disease, renal disease, hematology disease, endocrine disorder, psychiatric condition and neurological illness. Uncontrolled condition is defined as significant change in therapy or hospitalization for worsening disease during the 3 months before enrollment.

8. Have bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following intramuscular injections or venipuncture.

9. Received immunosuppressant or other immunomodulators, antiallergic therapy, or cytotoxicity therapy for 14 or more consecutive days within 6 months before receiving the investigational product (IP). Local administration of immunosuppressant or immunomodulator is allowed (e.g., ointment, eye drops, inhalation, or nasal spray). Drugs for local administration should not be given at a dose over the recommended level in package insert or participants should have no signs of systemic exposure.

10. Administration of immunoglobulin and/or blood product within 3 months before using the IP or plan to use that during the study.

11. Continuous use of anticoagulants, such as coumarins and related anticoagulants (i.e., warfarin) or novel oral anticoagulants (i.e., apixaban, rivaroxaban, dabigatran and edoxaban).

12. Used other investigational drug or interventional device within 1 month before using the IP or plan to use that during the study, or are using other investigational drug or are within 5 half-lives after the last dose of the investigational drug.

13. Used subunit or inactivated vaccine within 14 days before using the IP, or used attenuated live or mRNA vaccine within 1 months (30 days) before using the IP, or plan to receive any other vaccines (except for the seasonal influenza vaccine, or emergency use authorized vaccines) during the study.

14. Prior receipt of an investigational or licensed COVID-19 vaccine, or investigational or approved vaccine against a coronavirus, including but not limited to SARS-CoV-1 and MERS-CoV.

15. Suspected or known current alcohol or drug dependency.

16. Pregnancy, lactation or willingness/intention to become pregnant within 90 days after receiving the last dose of study vaccine.

17. Staff of study site, the sponsor, and contract research organization (CRO) taking part in study conduct.

18. Any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data at investigator's discretion.

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• Recombinant two-component COVID-19 vaccine (CHO cell)
Before reconstitution: Lyophilized powder for reconstitution in single-use vials After reconstitution with BFA03 adjuvant: Milk-white solution with no visible foreign matter
• Placebo
Before reconstitution: Lyophilized powder for reconstitution in single-use vials After reconstitution with BFA03 adjuvant: Milk-white solution with no visible foreign matter

Locations

Country	Name	City	State
Nepal	B.P. Koirala Institute of Health Sciences	Dharan Bazar
Russian Federation	Aramil City Hospital	Aramil
Russian Federation	LLC Medical Service solutions	Izhevsk
Russian Federation	'Federal State Budgetary Scientific Institution "Russian Scientific Centre of Surgery named after academician B.V. Petrovsky"	Moscow
Russian Federation	'Joint Stock Company "Clinical and diagnostic center "Euromedservice"	Moscow
Russian Federation	State Regional Budgetary Institution of Healthcare "Murmansk Regional Clinical Hospital named after P.A. Bayandin"	Murmansk
Russian Federation	LLC Professorskaya klinika	Perm
Russian Federation	UZI 4D Clinic LLC	Pyatigorsk
Russian Federation	Klinika Zvyezdnaya LLC	Saint Petersburg
Russian Federation	Limited Liability Company "Sfera-Med"	Saint Petersburg
Russian Federation	Research Center Eco-safety	Saint Petersburg

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu Rec-Biotechnology Co., Ltd.

Countries where clinical trial is conducted

Nepal,  Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Exploratory :	To evaluate the efficacy of ReCOV after the first dose vaccination in preventing RT-PCR confirmed symptomatic COVID-19 in adults aged 18 years and older.	> 14 days after the first dose vaccination
Primary	To evaluate the efficacy of ReCOV in preventing Reverse Transcription-Polymerase Chain Reaction (RT-PCR) confirmed symptomatic COVID-19 in adults	RT-PCR confirmed symptomatic COVID-19 cases (regardless of severity) that occurred > 14 days after 3 doses vaccination.	> 14 days after 3 doses vaccination.
Secondary	Evaluate the safety and reactogenicity	The occurrence of solicited local and systemic adverse events (AEs) within 7 days after each vaccination.	within 7 days after each vaccination
Secondary	Evaluate the safety and reactogenicity	The occurrence of unsolicited AEs from the 1st dose to 28 days after the 3rd vaccination	from the 1st dose to 28 days after the 3rd vaccination.
Secondary	Evaluate the safety and reactogenicity	The occurrence of serious adverse events (SAEs) and adverse events of special interest (AESIs) from the 1st dose to the end of study.	from the 1st dose to the end of study.
Secondary	To evaluate the efficacy of ReCOV in preventing RT-PCR confirmed symptomatic COVID-19 with various severity in adults	RT-PCR confirmed moderate, severe, critical COVID -19, or death that occurred > 14 days after 3 doses vaccination	> 14 days after 3 doses vaccination.
Secondary	To evaluate the efficacy of ReCOV in preventing RT-PCR confirmed symptomatic COVID-19 with various severity in adults	RT-PCR confirmed severe, critical COVID-19, or death that occurred > 14 days after 3 doses vaccination.	> 14 days after 3 doses vaccination.
Secondary	To evaluate the efficacy of ReCOV in preventing RT-PCR confirmed symptomatic COVID-19 with various severity in adults	RT-PCR confirmed symptomatic COVID-19 cases (regardless of severity) that occurred > 14 days after 3 doses vaccination in different age groups (18-59 years and = 60 years ).	> 14 days after 3 doses vaccination in different age groups (18-59 years and = 60 years ).
Secondary	To evaluate the immunogenicity of ReCOV	The seroconversion rate (SCR), geometric mean titer (GMT) and geometric mean increase (GMI) of neutralizing antibody against prototype and epidemic strain at 14 days, 3 months and 6 months after 3 doses vaccination.	at 14 days, 3 months and 6 months after 3 doses vaccination
Secondary	To compare the immunogenicity of ReCOV between Asian and Non-Asian in the immunogenicity subgroup	The SCR and GMT of neutralizing antibody against prototype at 14 days,3 months and 6 months after 3 doses vaccination.	at 14 days,3 months and 6 months after 3 doses vaccination
Secondary	Genotyping of SARS-CoV-2 virus nucleic acid sequence of COVID-19 cases to evaluate the possible viral mutations	SARS-CoV-2 virus nucleic acid sequence of RT-PCR confirmed symptomatic COVID-19 cases that occurred >14 days after 3 doses vaccination derived from isolates or direct nasopharyngeal (NP) (preferred)/ oropharyngeal (OP) swab, or respiratory samples (including saliva samples, or bronchoalveolar lavage fluid, if applicable).	>14 days after 3 doses vaccination