COVID-19Phase 2NCT05239806
A Phase II Clinical Trial to Evaluate the Immunogenicity and Safety of SCTV01C and SCTV01E in Population Aged ≥12 Years Previously Fully Vaccinated With Inactivated COVID-19 Vaccine
A Phase 2 study testing SCTV01C, SCTV01E and Sinopharm inactivated COVID-19 vaccine in people with COVID-19 and SARS-CoV-2 Infection, run by Sinocelltech Ltd..
Trial summary
The objective of study is to evaluate the immunogenicity and safety of SCTV01C or SCTV01E as booster compared with Sinopharm inactivated COVID-19 vaccine as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations. Read more about this study
- Who is it for?
- Ages 12 years and olderHealthy volunteers can take part
- Conditions the study is for
- COVID-19, SARS-CoV-2 Infection
- What is being tested?
- SCTV01C, SCTV01E and Sinopharm inactivated COVID-19 vaccine
- Type of treatment
- Vaccines, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 400 participants
- Where
- No sites listed yet
- Study dates
- 1 Apr 2022to 1 Aug 2023
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Male or female aged ≥12 years old when signing ICF;
- Participants who were fully vaccinated with inactivated COVID-19 vaccine (Sinopharm inactivated COVID-19 vaccine), and the interval between the last dose and this study vaccination is ≥3 months and ≤12 months;
- The participant and/or his legal guardian and/or his entrusted person can sign written ICF, and can fully understand the trial procedure, the risk of participating in the trial, and other interventions that can be selected if they do not participate in the trial;
- The participant and/or his legal guardian and/or his entrusted person have the ability to read, understand, and fill in record cards;
- Healthy participants or participants with pre-existing medical conditions who are in stable condition. The "pre-existing medical conditions" include but not limited to hypertension, diabetes, chronic cholecystitis and cholelithiasis, chronic gastritis that meet the described criteria. A stable medical condition is defined as disease not requiring significant change in therapy or no need for hospitalization as a consequence of worsening disease state for at least 3 months prior to enrollment;
- Fertile men and women of childbearing potential voluntarily agree to take effective contraceptive measures from signing ICF to 6 months after the 1st study vaccination; the pregnancy test results of women of childbearing potential are negative on screening.
Who cannot join
- Previously diagnosed with COVID-19;
- Presence of fever within 3 days before the study vaccination;
- A history of infection or disease related to severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), or other disease corresponding use of immunosuppressants;
- A history of allergic reactions to any vaccine or drug, such as allergy, urticaria, severe skin eczema, dyspnea, laryngeal edema, and angioneurotic edema;
- A medical or family history of seizure, epilepsy, encephalopathy and psychosis;
- Immunocompromised patients suffering from immunodeficiency diseases, important organ diseases, 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.;
Show all 21Show fewer
- Long-term use of immunosuppressant therapy or immunomodulatory drugs for ≥14 days within the first six months prior to enrollment. Whereas short-term (≤14 days) use of oral, inhaled and topical steroids are allowed;
- Patients on antituberculosis therapy;
- 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 (except for skin basal cell carcinoma and carcinoma in-situ of cervix), 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;
- 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 is at the acute state of disease, such as acute onset of chronic heart failure, acute sore throat, hypertensive encephalopathy, acute pneumonia, acute renal insufficiency, acute cholecystitis;
- Participants received other drugs or vaccines used to prevent COVID-19 (exception for Sinopharm inactivated COVID-19 vaccine) ;
- 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 the study results, or non-conformance with the maximal benefits of the participants;
- Those who are tested positive for HIV in terms of serology.
Trial locations and contacts
No sites are listed yet.
About this study
Official title: A Randomized, Double-blind Phase II Clinical Trial to Evaluate the Immunogenicity and Safety of SCTV01C (A Bivalent SARS-CoV-2 Trimeric Spike Protein Vaccine) and SCTV01E (A COVID-19 Alpha/Beta/Delta/Omicron Variants S-Trimer Vaccine) in Population Aged ≥12 Years Previously Fully Vaccinated With Inactivated COVID-19 Vaccine
The objective of study is to evaluate the immunogenicity and safety of SCTV01C or SCTV01E as booster compared with Sinopharm inactivated COVID-19 vaccine as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations.
Read the detailed description
The study is a randomized, double-blind, and approved vaccine-controlled Phase II booster study. It will evaluate the immunogenicity and safety of one dose of SCTV01C or SCTV01E as booster compared with one dose of Sinopharm inactivated COVID-19 vaccine or one dose of Commirnaty as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations (1-dose of SCTV01C and 1-dose of SCTV01E, or 2-dose of SCTV01E, or 1-dose of Sinopharm inactivated COVID-19 vaccine and 1-dose of SCTV01E, 1-dose of Comirnaty and 1-dose of SCTV01E).
- Conditions
- COVID-19, SARS-CoV-2 Infection
- Being tested
- SCTV01C, SCTV01E, Sinopharm inactivated COVID-19 vaccine, Comirnaty
- Keywords
- COVID-19, SARS-CoV-2 infection, Vaccine
- Medical subject headings
- COVID-19
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SCTV01CBiological
Day 0; intramuscular injection
SCTV01EBiological
Day 0; intramuscular injection
Sinopharm inactivated COVID-19 vaccineBiological
Day 0; intramuscular injection
ComirnatyBiological
Day 0; intramuscular injection
SCTV01EBiological
Day 180; intramuscular injection
| Study group | Role | What they receive |
|---|---|---|
| SCTV01C | Experimental | Participants will receive one dose of SCTV01C on Day 0 and one dose of SCTV01E on Day 180. Receives: Biological: SCTV01C; Biological: SCTV01E |
| SCTV01E | Experimental | Participants will receive one dose of SCTV01E on Day 0 and one dose of SCTV01E on Day 180. Receives: Biological: SCTV01E |
| Sinopharm inactivated COVID-19 vaccine | Active comparator | Participants will receive one dose of Sinopharm inactivated COVID-19 vaccine on Day 0 and one dose of SCTV01E on Day 180. Receives: Biological: Sinopharm inactivated COVID-19 vaccine; Biological: SCTV01E |
| Comirnaty | Active comparator | Participants will receive one dose of Comirnaty on Day 0 and one dose of SCTV01E on Day 180. Receives: Biological: Comirnaty; Biological: SCTV01E |
What is being measured
The primary outcome is the main question the study is designed to answer.
GMT of neutralizing antibodies against Delta (B.1.617.2) variant on Day 28.
Measured: Day 28 after the study vaccination
GMT of neutralizing antibodies against Omicron (B.1.1.529) variant on Day 28.
Measured: Day 28 after the study vaccination
GMT of neutralizing antibodies against Delta (B.1.617.2) variant on Day 208.
Measured: Day 208 after the study vaccination
GMT of neutralizing antibodies against Omicron (B.1.1.529) variant on Day 208.
Measured: Day 208 after the study vaccination
Secondary outcomes (11)
Number of IFN-γ positive (characterizing Th1) and IL-4 positive (characterizing Th2) T cell subsets on Day 28 and Day 208.
Measured: Day 28 and D208 after the study vaccination
Seroresponse rates of neutralizing antibodiesto Delta variant on Day 28.
Measured: Day 28 after the study vaccination
Seroresponse rates of neutralizing antibodies to Omicron variant rates on Day 28.
Measured: Day 28 after the study vaccination
Seroresponse rates of neutralizing antibodies to Delta variant on Day 208.
Measured: Day 208 after the study vaccination
Seroresponse rates of neutralizing antibodies to Omicron variant on Day 208.
Measured: Day 208 after the study vaccination
Incidence and severity of solicited AEs of SCTV01C from Day 0 to Day 7 and Day 180 to Day 187.
Measured: Day 0 to Day 7 after the 1st study vaccination and Day 180 to Day 187 after the 2nd study vaccination
Incidence and severity of all unsolicited AEs of SCTV01C from Day 0 to Day 28 and Day 180 to Day 208.
Measured: Day 0 to Day 28 after the 1st study vaccination and Day 180 to Day 208 after the 2nd study vaccination
Incidence and severity of SAEs and AESIs of SCTV01C within 365 days.
Measured: Day 0 to Day 365 after the 1st study vaccination
Incidence and severity of solicited AEs of SCTV01E from Day 0 to Day 7 and Day 180 to Day 187.
Measured: Day 0 to Day 7 after the 1st study vaccination and Day 180 to Day 187 after the 2nd study vaccination
Incidence and severity of all unsolicited AEs of SCTV01E from Day 0 to Day 28 and Day 180 to Day 208.
Measured: Day 0 to Day 28 after the 1st study vaccination and Day 180 to Day 208 after the 2nd study vaccination
Incidence and severity of SAEs and AESIs of SCTV01E within 365 days.
Measured: Day 0 to Day 365 after the 1st study vaccination
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Feb 2022
- Study start1 Apr 2022 (estimated)
- Primary completion1 Aug 2022 (estimated)
- Study completion1 Aug 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for COVID-19Studies of the same condition, open and under way.
- More trials run by Sinocelltech Ltd.The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 400 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Sinocelltech Ltd.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05239806
- Sponsor's protocol ID
- SCTV01C/E-01-In-LAO-1
- Status last verified
- Feb 2022
- First submitted
- 14 Feb 2022
- Last updated
- 11 Apr 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Apr 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Double-blind Phase II Clinical Trial to Evaluate the Immunogenicity and Safety of SCTV01C (A Bivalent SARS-CoV-2 Trimeric Spike Protein Vaccine) and SCTV01E (A COVID-19 Alpha/Beta/Delta/Omicron Variants S-Trimer Vaccine) in Population Aged ≥12 Years Previously Fully Vaccinated With Inactivated COVID-19 Vaccine
- ClinicalTrials.gov ID
- NCT05239806
- Acronym / sponsor ID
- SCTV01C/E-01-In-LAO-1
- Conditions
- COVID-19, SARS-CoV-2 Infection
- Keywords
- COVID-19, SARS-CoV-2 infection, Vaccine
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 400 participants (estimated)
- Lead sponsor
- Sinocelltech Ltd.Industry (pharma, biotech, devices)
- Study start
- 1 Apr 2022 (estimated)
- Primary completion
- 1 Aug 2022 (estimated)
- Study completion
- 1 Aug 2023 (estimated)
- First posted
- 15 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of study is to evaluate the immunogenicity and safety of SCTV01C or SCTV01E as booster compared with Sinopharm inactivated COVID-19 vaccine as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations.
Detailed description
The study is a randomized, double-blind, and approved vaccine-controlled Phase II booster study. It will evaluate the immunogenicity and safety of one dose of SCTV01C or SCTV01E as booster compared with one dose of Sinopharm inactivated COVID-19 vaccine or one dose of Commirnaty as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations (1-dose of SCTV01C and 1-dose of SCTV01E, or 2-dose of SCTV01E, or 1-dose of Sinopharm inactivated COVID-19 vaccine and 1-dose of SCTV01E, 1-dose of Comirnaty and 1-dose of SCTV01E).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| SCTV01C | Experimental | Biological: SCTV01C, Biological: SCTV01EParticipants will receive one dose of SCTV01C on Day 0 and one dose of SCTV01E on Day 180. |
| SCTV01E | Experimental | Biological: SCTV01EParticipants will receive one dose of SCTV01E on Day 0 and one dose of SCTV01E on Day 180. |
| Sinopharm inactivated COVID-19 vaccine | Active comparator | Biological: Sinopharm inactivated COVID-19 vaccine, Biological: SCTV01EParticipants will receive one dose of Sinopharm inactivated COVID-19 vaccine on Day 0 and one dose of SCTV01E on Day 180. |
| Comirnaty | Active comparator | Biological: Comirnaty, Biological: SCTV01EParticipants will receive one dose of Comirnaty on Day 0 and one dose of SCTV01E on Day 180. |
Who may qualify
- Ages
- 12 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (6 listed)
- Male or female aged ≥12 years old when signing ICF;
- Participants who were fully vaccinated with inactivated COVID-19 vaccine (Sinopharm inactivated COVID-19 vaccine), and the interval between the last dose and this study vaccination is ≥3 months and ≤12 months;
- The participant and/or his legal guardian and/or his entrusted person can sign written ICF, and can fully understand the trial procedure, the risk of participating in the trial, and other interventions that can be selected if they do not participate in the trial;
- The participant and/or his legal guardian and/or his entrusted person have the ability to read, understand, and fill in record cards;
- Healthy participants or participants with pre-existing medical conditions who are in stable condition. The "pre-existing medical conditions" include but not limited to hypertension, diabetes, chronic cholecystitis and cholelithiasis, chronic gastritis that meet the described criteria. A stable medical condition is defined as disease not requiring significant change in therapy or no need for hospitalization as a consequence of worsening disease state for at least 3 months prior to enrollment;
Key exclusion criteria (21 listed)
- Previously diagnosed with COVID-19;
- Presence of fever within 3 days before the study vaccination;
- A history of infection or disease related to severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), or other disease corresponding use of immunosuppressants;
- A history of allergic reactions to any vaccine or drug, such as allergy, urticaria, severe skin eczema, dyspnea, laryngeal edema, and angioneurotic edema;
- A medical or family history of seizure, epilepsy, encephalopathy and psychosis;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SCTV01CDay 0; intramuscular injection | Biological | SCTV01C |
| SCTV01EDay 0; intramuscular injection | Biological | SCTV01E |
| Sinopharm inactivated COVID-19 vaccineDay 0; intramuscular injection | Biological | Sinopharm inactivated COVID-19 vaccine |
| ComirnatyDay 0; intramuscular injection | Biological | Comirnaty |
| SCTV01EDay 180; intramuscular injection | Biological | Comirnaty, SCTV01C, SCTV01E, Sinopharm inactivated COVID-19 vaccine |
Primary outcome
GMT of neutralizing antibodies against Delta (B.1.617.2) variant on Day 28.
Time frame: Day 28 after the study vaccination
GMT of neutralizing antibodies against Omicron (B.1.1.529) variant on Day 28.
Time frame: Day 28 after the study vaccination
GMT of neutralizing antibodies against Delta (B.1.617.2) variant on Day 208.
Time frame: Day 208 after the study vaccination
GMT of neutralizing antibodies against Omicron (B.1.1.529) variant on Day 208.
Time frame: Day 208 after the study vaccination
11 secondary outcomes
Number of IFN-γ positive (characterizing Th1) and IL-4 positive (characterizing Th2) T cell subsets on Day 28 and Day 208.
Time frame: Day 28 and D208 after the study vaccination
Seroresponse rates of neutralizing antibodiesto Delta variant on Day 28.
Time frame: Day 28 after the study vaccination
Seroresponse rates of neutralizing antibodies to Omicron variant rates on Day 28.
Time frame: Day 28 after the study vaccination
Seroresponse rates of neutralizing antibodies to Delta variant on Day 208.
Time frame: Day 208 after the study vaccination
Seroresponse rates of neutralizing antibodies to Omicron variant on Day 208.
Time frame: Day 208 after the study vaccination
Incidence and severity of solicited AEs of SCTV01C from Day 0 to Day 7 and Day 180 to Day 187.
Time frame: Day 0 to Day 7 after the 1st study vaccination and Day 180 to Day 187 after the 2nd study vaccination
Incidence and severity of all unsolicited AEs of SCTV01C from Day 0 to Day 28 and Day 180 to Day 208.
Time frame: Day 0 to Day 28 after the 1st study vaccination and Day 180 to Day 208 after the 2nd study vaccination
Incidence and severity of SAEs and AESIs of SCTV01C within 365 days.
Time frame: Day 0 to Day 365 after the 1st study vaccination
Incidence and severity of solicited AEs of SCTV01E from Day 0 to Day 7 and Day 180 to Day 187.
Time frame: Day 0 to Day 7 after the 1st study vaccination and Day 180 to Day 187 after the 2nd study vaccination
Incidence and severity of all unsolicited AEs of SCTV01E from Day 0 to Day 28 and Day 180 to Day 208.
Time frame: Day 0 to Day 28 after the 1st study vaccination and Day 180 to Day 208 after the 2nd study vaccination
Incidence and severity of SAEs and AESIs of SCTV01E within 365 days.
Time frame: Day 0 to Day 365 after the 1st study vaccination
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Apr 2022.
Related trials for COVID-19
Not yet recruitingPhase 1
Phase I Open-Label Safety Trial of Pembrolizumab for Neurological Post- Acute Sequelae of SARS-CoV-2 (PD1-PASC I)
Post-Acute COVID-19 Syndrome
Active, not recruitingPhase 1
A Safety and Immunogenicity Trial of OCU500, ChAd36 Vector Encoding SARS-CoV-2 Spike Vaccine Via Intranasal and Inhalational Routes in Previously Vaccinated Adults
COVID-19
Active, not recruiting
Intervention to Address Disparate Mental Health Consequences of COVID-19 Pandemic on Latinx and African Newcomers
Mental Health Issue, Mental Health Disorder
Recruiting
Home-Based Exercise Tele-Rehabilitation After COVID-19
Post SARS-CoV2 (COVID-19)
Not yet recruitingPhase 1
A Safety, Reactogenicity and Immunogenicity Trial of RVX-sCPD9 Booster Intranasal COVID-19 Vaccine
COVID -19
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing SCTV01C, SCTV01E and Sinopharm inactivated COVID-19 vaccine in people with COVID-19 and SARS-CoV-2 Infection, run by Sinocelltech Ltd..
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 21 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 11 Apr 2022. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Min Ke (+86 18501160269, min_ke@sinocelltech.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
GMT of neutralizing antibodies against Delta (B.1.617.2) variant on Day 28. (time frame: Day 28 after the study vaccination). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Apr 2022.