A Study to Evaluate the Immunogenicity and Safety of a Recombinant Protein COVID-19 Vaccine SCTV01E-1 in Population Aged Above 18 Years
Primary Purpose
COVID-19, SARS-CoV-2 Infection
Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
SCTV01E-1 on D0
SCTV01E-1 on D28
SCTV01E-1 on D150
SCTV01E on D0
SCTV01E on D28
SCTV01E on D150
SCTV01E-1 on D120
SCTV01E on D120
Sponsored by
About this trial
This is an interventional prevention trial for COVID-19 focused on measuring SARS-CoV-2, COVID-19, vaccine
Eligibility Criteria
Inclusion Criteria:
- Male or female aged ≥18 years when signing ICF;
- For Cohort 1: Participants who have not been vaccinated with any COVID-19 vaccine; For Cohort 2: Participants who were fully vaccinated with 2 or 3 doses of inactivated COVID-19 vaccine and the interval between the last dose of previously vaccination and the 1st study vaccination is 3 to 24 months;
- Healthy participants or participants with pre-existing medical conditions that are in stable condition. The "pre-existing medical conditions" include but not limited to hypertension, diabetes, chronic cholecystitis and cholelithiasis, chronic gastritis, etc. A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization as a consequence of worsening disease state for at least 3 months prior to study participation;
- The participant or his/her legal representative can sign written ICF, and can fully understand the trial procedure, the risk of participating in the trial, and other interventions that are available if they do not participate in the trial;
- The participant can read, understand, and fill in record cards by himself/herself or with help;
- Fertile men and women of childbearing potential voluntarily agree to take effective contraceptive measures from signing ICF to 6 months after the last dose of study vaccination.
Exclusion Criteria:
- Presence of fever (oral temperature ≥37.5℃) within 3 days before the 1st study vaccination;
- For Cohort 2 only: Known history of COVID-19 or asymptomatic SRAS-CoV-2 infection;
- A history of allergic reactions to any vaccines or drugs, such as allergy, urticaria, severe skin eczema, dyspnea, laryngeal edema, and angioneurotic edema;
- Immunocompromised patients suffering from immunodeficiency diseases, significant diseases, or immune diseases (including Guillain-Barre Syndrome [GBS], systemic lupus erythematosus, rheumatoid arthritis, asplenia or splenectomy caused by any circumstances, and other immune diseases that may have an impact on immune response in the investigator's opinion), etc;
- Long-term use of immunosuppressant therapy or immunomodulatory drugs for >14 days within the six months prior to enrollment. Whereas short-term (≤14 days) use of oral, inhaled and topical steroids are allowed;
- Those who have a history of HIV or tested positive for HIV;
- For Cohort 1, participants received any drugs or vaccines used to prevent COVID-19; for Cohort 2, participants received other drugs or vaccines used to prevent COVID-19 besides inactivated COVID-19 vaccines;
- A history of Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS), or related vaccination;
- A medical or family history of seizure, epilepsy, encephalopathy and psychosis;
- Presence of severe or uncontrollable cardiovascular diseases, or severe or uncontrollable disorders related to endocrine system, blood and lymphatic system, liver and kidney, respiratory system, metabolic and skeletal systems, or malignancies (skin basal cell carcinoma and carcinoma in-situ of cervix are exceptions and will not be excluded), such as severe heart failure, severe pulmonary heart disease, unstable angina, liver failure, or uremia;
- Contraindications for intramuscular injection or intravenous blood sampling, including thrombocytopenia and other blood coagulation disorders;
- Patients on antituberculosis therapy;
- Participants who received any immunoglobulin or blood products in the previous 3 months before enrollment, or plan to receive similar products during the study;
- Participants who received other investigational drugs within 1 month before the study vaccination;
- Participants who have acute illness, such as acute onset of chronic heart failure, acute sore throat, hypertensive encephalopathy, acute pneumonia, acute renal insufficiency, acute cholecystitis;
- Participants vaccinated with influenza vaccine within 14 days or with other vaccines within 28 days before the study vaccination;
- Those who donated blood or had blood loss (≥450 mL) within 3 months before the vaccination or plan to donate blood during the study period;
- Those who are pregnant or breast-feeding or plan to be pregnant during the study period;
- Those who plan to donate ovum or sperms during the study period;
- Those who cannot follow the trial procedures, or cannot cooperate to complete the study due to planned relocation or long-term outing;
- Those unsuitable for participating in the clinical trial as determined by the investigator because of other abnormalities that are likely to confuse or confound the study results, or non-conformance with the maximal benefits of the participants.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Active Comparator
Experimental
Active Comparator
Arm Label
Cohort 1: Group SCTV01E-1
Cohort 1: Group SCTV01E
Cohort 2: Group SCTV01E-1
Cohort 2: Group SCTV01E
Arm Description
3 doses of SCTV01E-1
3 doses of SCTV01E
2 doses of SCTV01E-1
2 doses of SCTV01E
Outcomes
Primary Outcome Measures
Cohort 1: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 42.
Cohort 1: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 178.
Cohort 2: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 28.
Cohort 2: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 148.
Secondary Outcome Measures
Cohort 1: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 42.
Cohort 1: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 178.
Cohort 1: Incidence and severity of solicited AEs within 7 days after each of the study vaccination.
Cohort 1: Incidence and severity of unsolicited AEs within 28 days after each of the study vaccination.
Cohort 1: Incidence and severity of SAEs and AESIs within 180 days after each of the study vaccination.
Cohort 2: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 28.
Cohort 2: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 148.
Cohort 2: Incidence and severity of solicited AEs within 7 days after each of the study vaccination.
Cohort 2: Incidence and severity of unsolicited AEs within 28 days after each of the study vaccination.
Cohort 2: Incidence and severity of SAEs and AESIs within 180 days after each of the study vaccination.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05522829
Brief Title
A Study to Evaluate the Immunogenicity and Safety of a Recombinant Protein COVID-19 Vaccine SCTV01E-1 in Population Aged Above 18 Years
Official Title
A Randomized, Double-blind Phase II Clinical Trial to Evaluate the Immunogenicity and Safety of SCTV01E-1 (Alpha/Beta/Delta/Omicron (BA.1/BA.4/BA.5) Variants S-Trimer COVID-19 Vaccine) in Population Aged 18 Years and Older
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 15, 2022 (Anticipated)
Primary Completion Date
December 15, 2022 (Anticipated)
Study Completion Date
December 15, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sinocelltech Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The study is a randomized, double-blind Phase II study. It will evaluate the immunogenicity and safety of SCTV01E-1. Approximately 400 participants aged 18 years and older will be enrolled in this study. 160 participants who have not been vaccinated with any COVID-19 vaccine will be enrolled in Cohort 1 and randomly assigned to receive SCTV01E-1 or SCTV01E in a ratio of 1:1. 240 participants who were fully vaccinated with 2 or 3 doses of inactivated COVID-19 vaccines at least three months ago will be enrolled in Cohort 2 and randomly assigned to receive SCTV01E-1 or SCTV01E in a ratio of 1:1.
Detailed Description
The study is a randomized, double-blind Phase II study. It will evaluate the immunogenicity and safety of SCTV01E-1. Approximately 400 participants aged 18 years and older will be enrolled in this study.
160 participants who have not been vaccinated with any COVID-19 vaccine will be enrolled in Cohort 1 and randomly assigned to the Group SCTV01E-1 and Group SCTV01E in a ratio of 1:1. All participants will receive 3 doses of vaccinations: Vaccination 1 on D0, Vaccination 2 on D28 and Vaccination 3 on D150. Participants in Group SCTV01E-1 will receive 3 doses of SCTV01E-1, and participants in Group SCTV01E will receive 3 doses of SCTV01E.
240 participants who were fully vaccinated with 2 or 3 doses of inactivated COVID-19 vaccines at least three months ago will be enrolled in Cohort 2 and randomly assigned to Group SCTV01E-1 and Group SCTV01E in a ratio of 1:1. All participants will receive 2 doses of vaccinations: Vaccination 1 on D0 and Vaccination 2 on D120. Participants in Group SCTV01E-1 will receive 2 doses of SCTV01E-1, and participants in Group SCTV01E will receive 2 doses of SCTV01E.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19, SARS-CoV-2 Infection
Keywords
SARS-CoV-2, COVID-19, vaccine
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cohort 1: Group SCTV01E-1
Arm Type
Experimental
Arm Description
3 doses of SCTV01E-1
Arm Title
Cohort 1: Group SCTV01E
Arm Type
Active Comparator
Arm Description
3 doses of SCTV01E
Arm Title
Cohort 2: Group SCTV01E-1
Arm Type
Experimental
Arm Description
2 doses of SCTV01E-1
Arm Title
Cohort 2: Group SCTV01E
Arm Type
Active Comparator
Arm Description
2 doses of SCTV01E
Intervention Type
Biological
Intervention Name(s)
SCTV01E-1 on D0
Intervention Description
Day 0; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E-1 on D28
Intervention Description
Day 28; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E-1 on D150
Intervention Description
Day 150; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E on D0
Intervention Description
Day 0; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E on D28
Intervention Description
Day 28; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E on D150
Intervention Description
Day 150; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E-1 on D120
Intervention Description
Day 120; intramuscular injection
Intervention Type
Biological
Intervention Name(s)
SCTV01E on D120
Intervention Description
Day 120; intramuscular injection
Primary Outcome Measure Information:
Title
Cohort 1: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 42.
Time Frame
Day 42 after the study vaccination
Title
Cohort 1: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 178.
Time Frame
Day 178 after the study vaccination
Title
Cohort 2: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 28.
Time Frame
Day 28 after the study vaccination
Title
Cohort 2: Geometric mean titers (GMT) of neutralizing antibodies (nAb) against Omicron subvariant (BA.5) on Day 148.
Time Frame
Day 148 after the study vaccination
Secondary Outcome Measure Information:
Title
Cohort 1: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 42.
Time Frame
Day 42 after the study vaccination
Title
Cohort 1: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 178.
Time Frame
Day 178 after the study vaccination
Title
Cohort 1: Incidence and severity of solicited AEs within 7 days after each of the study vaccination.
Time Frame
Day 0 to Day 7 after each of the study vaccination
Title
Cohort 1: Incidence and severity of unsolicited AEs within 28 days after each of the study vaccination.
Time Frame
Day 0 to Day 28 after each of the study vaccination
Title
Cohort 1: Incidence and severity of SAEs and AESIs within 180 days after each of the study vaccination.
Time Frame
During the whole study
Title
Cohort 2: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 28.
Time Frame
Day 28 after the study vaccination
Title
Cohort 2: Seroresponse rates of nAb against Omicron subvariant (BA.5) on Day 148.
Time Frame
Day 148 after the study vaccination
Title
Cohort 2: Incidence and severity of solicited AEs within 7 days after each of the study vaccination.
Time Frame
Day 0 to Day 7 after each of the study vaccination
Title
Cohort 2: Incidence and severity of unsolicited AEs within 28 days after each of the study vaccination.
Time Frame
Day 0 to Day 28 after each of the study vaccination
Title
Cohort 2: Incidence and severity of SAEs and AESIs within 180 days after each of the study vaccination.
Time Frame
During the whole study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male or female aged ≥18 years when signing ICF;
For Cohort 1: Participants who have not been vaccinated with any COVID-19 vaccine; For Cohort 2: Participants who were fully vaccinated with 2 or 3 doses of inactivated COVID-19 vaccine and the interval between the last dose of previously vaccination and the 1st study vaccination is 3 to 24 months;
Healthy participants or participants with pre-existing medical conditions that are in stable condition. The "pre-existing medical conditions" include but not limited to hypertension, diabetes, chronic cholecystitis and cholelithiasis, chronic gastritis, etc. A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization as a consequence of worsening disease state for at least 3 months prior to study participation;
The participant or his/her legal representative can sign written ICF, and can fully understand the trial procedure, the risk of participating in the trial, and other interventions that are available if they do not participate in the trial;
The participant can read, understand, and fill in record cards by himself/herself or with help;
Fertile men and women of childbearing potential voluntarily agree to take effective contraceptive measures from signing ICF to 6 months after the last dose of study vaccination.
Exclusion Criteria:
Presence of fever (oral temperature ≥37.5℃) within 3 days before the 1st study vaccination;
For Cohort 2 only: Known history of COVID-19 or asymptomatic SRAS-CoV-2 infection;
A history of allergic reactions to any vaccines or drugs, such as allergy, urticaria, severe skin eczema, dyspnea, laryngeal edema, and angioneurotic edema;
Immunocompromised patients suffering from immunodeficiency diseases, significant diseases, or immune diseases (including Guillain-Barre Syndrome [GBS], systemic lupus erythematosus, rheumatoid arthritis, asplenia or splenectomy caused by any circumstances, and other immune diseases that may have an impact on immune response in the investigator's opinion), etc;
Long-term use of immunosuppressant therapy or immunomodulatory drugs for >14 days within the six months prior to enrollment. Whereas short-term (≤14 days) use of oral, inhaled and topical steroids are allowed;
Those who have a history of HIV or tested positive for HIV;
For Cohort 1, participants received any drugs or vaccines used to prevent COVID-19; for Cohort 2, participants received other drugs or vaccines used to prevent COVID-19 besides inactivated COVID-19 vaccines;
A history of Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS), or related vaccination;
A medical or family history of seizure, epilepsy, encephalopathy and psychosis;
Presence of severe or uncontrollable cardiovascular diseases, or severe or uncontrollable disorders related to endocrine system, blood and lymphatic system, liver and kidney, respiratory system, metabolic and skeletal systems, or malignancies (skin basal cell carcinoma and carcinoma in-situ of cervix are exceptions and will not be excluded), such as severe heart failure, severe pulmonary heart disease, unstable angina, liver failure, or uremia;
Contraindications for intramuscular injection or intravenous blood sampling, including thrombocytopenia and other blood coagulation disorders;
Patients on antituberculosis therapy;
Participants who received any immunoglobulin or blood products in the previous 3 months before enrollment, or plan to receive similar products during the study;
Participants who received other investigational drugs within 1 month before the study vaccination;
Participants who have acute illness, such as acute onset of chronic heart failure, acute sore throat, hypertensive encephalopathy, acute pneumonia, acute renal insufficiency, acute cholecystitis;
Participants vaccinated with influenza vaccine within 14 days or with other vaccines within 28 days before the study vaccination;
Those who donated blood or had blood loss (≥450 mL) within 3 months before the vaccination or plan to donate blood during the study period;
Those who are pregnant or breast-feeding or plan to be pregnant during the study period;
Those who plan to donate ovum or sperms during the study period;
Those who cannot follow the trial procedures, or cannot cooperate to complete the study due to planned relocation or long-term outing;
Those unsuitable for participating in the clinical trial as determined by the investigator because of other abnormalities that are likely to confuse or confound the study results, or non-conformance with the maximal benefits of the participants.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dilihumare ·Niyazi
Phone
+86 10 58628288-9014
Email
dilihumare_niyazi@sinocelltech.com
12. IPD Sharing Statement
Learn more about this trial
A Study to Evaluate the Immunogenicity and Safety of a Recombinant Protein COVID-19 Vaccine SCTV01E-1 in Population Aged Above 18 Years
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