A Study to Evaluate MVC-COV1901 Vaccine Against COVID-19 in Adult
- Conditions
- Covid19 Vaccine
- Interventions
- Biological: MVC-COV1901(S protein with adjuvant)Biological: MVC-COV1901(Saline)
- Registration Number
- NCT04695652
- Lead Sponsor
- Medigen Vaccine Biologics Corp.
- Brief Summary
The purpose of this study is to assess the safety and immunogenicity of MVC-COV1901 vaccine compared to placebo in participants who are generally healthy or with stable pre-existing health conditions.
- Detailed Description
This is a Phase II, prospective, placebo-controlled, double-blinded (investigator/site staff and participants), multi-center, multi-regional study; the Sponsor will be blinded until the interim analysis. Participants who are generally healthy or with stable pre-existing health conditions will be randomized, stratified by age (≥ 20 to \< 65 years and ≥ 65 years of age).All eligible participants will be randomized to receive 2 doses of either MVC-COV1901 or placebo in a predefined ratio.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 3854
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Male or female participant ≥ 20 to < 65 years, or ≥ 65 years of age at randomization.
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Healthy adults or adults with pre-existing medical conditions who are in stable condition. A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization for worsening disease 3 months before enrollment and expected to remain stable for the duration of the study.
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Female participant must:
- Be either of non-childbearing potential, i.e. surgically sterilized (defined as having undergone hysterectomy and/or bilateral oophorectomy and/or bilateral salpingectomy; tubal ligation alone is not considered sufficient) or one year post-menopausal;
- Or, if of childbearing potential, be abstinent or agree to use medically effective contraception from 14 days before screening to 30 days following the last injection of study intervention. Acceptable forms include:
i. Implanted hormonal methods of contraception or placement of an intrauterine device or intrauterine system ii. Established use of hormonal methods (injectable, pill, patch or ring) combined with barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository c. Have a negative pregnancy test
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Participant is willing and able to comply with all required study visits and follow-up required by this protocol.
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Participant has not travelled overseas within 14 days of screening and will not have any oversea travelling throughout the study period.
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Participant or the participant's legal representative must understand the procedures of the study and provide written informed consent.
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Pregnant or breast feeding or have plan to become pregnant in 30 days after last administration of study intervention.
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Employees at the investigator's site, of the Sponsor or the contract research organization (CRO) directly involved in the conduct of the study.
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Currently receiving or received any investigational intervention within 30 days prior to the first dose of study intervention.
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Administered any licensed live-attenuated vaccines within 28 days or other licensed non-live-attenuated vaccines within 7 days prior to the first dose of study intervention.
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Administered any blood product or intravenous immunoglobulin administration within 12 weeks prior to the first dose of study intervention.
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Currently receiving or anticipate to receive concomitant immunosuppressive or immune-modifying therapy (excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or < 2 weeks of daily receipt of prednisone less than 20 mg or equivalent) within 12 weeks prior to the first dose of study intervention.
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Currently receiving or anticipate to receive treatment with tumor necrosis factor (TNF)-α inhibitors, e.g. infliximab, adalimumab, etanercept within 12 weeks prior to the first dose of study intervention.
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Major surgery or any radiation therapy within 12 weeks prior to the first dose of study intervention Medical Conditions
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Immunosuppressive illness or immunodeficient state, including hematologic malignancy, history of solid organ, bone marrow transplantation, or asplenia.
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A history of autoimmune disease (systemic lupus, rheumatoid arthritis, scleroderma, polyarthritis, thyroiditis, Guillain-Barré syndrome, etc.).
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A history of malignancy with potential risk for recurrence after curative treatment, or current diagnosis of or treatment for cancer (exceptions are squamous and basal cell carcinomas of the skin and treated uterine cervical carcinoma in situ, at the discretion of the investigator).
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Bleeding disorder considered a contraindication to intramuscular injection or phlebotomy.
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Human immunodeficiency virus (HIV) antibody positive participants with CD4 count < 350 cells/mm3 or a detectable HIV viral load within the past year (low level variations from 50-500 viral copies/mL or equivalent which do not lead to changes in antiretroviral therapy [ART] are permitted).
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Hepatitis B surface antigen (HBsAg) positive participant with positive hepatitis B e antigen (HBeAg) or abnormal liver function.
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Hepatitis C virus (HCV) antibody positive participants with detectable HCV ribonucleic acid (RNA) viremia in recent 12 weeks.
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Participant with ongoing acute diseases or serious medical conditions which will interfere with adherence to study requirements, or the evaluation of any study endpoint. Acute diseases or serious medical conditions include cardiovascular (e.g. New York Heart Association Grade III or IV), pulmonary (e.g. chronic obstructive pulmonary disease stage III or IV), hepatic (e.g. Child-Pugh Class C), neurologic (e.g. dementia), metabolic (e.g. diabetes mellitus with hemoglobin A1c [HbA1c] > 8%), renal (Stage 3 or worse chronic kidney disease), psychiatric condition (e.g. alcoholism, drug abuse), current severe infections, medical history, physical findings, or laboratory abnormality that in the investigators' opinion are not in stable condition and participating in the study could adversely affect the safety of the participant.
Medigen Vaccine Biologics Corp. 34
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Participant with previous known or potential exposure to SARS-CoV-1 or 2 viruses (EXCEPT for those who have been tested negative and completed the 14-day self-managements/ home quarantines/ home isolations) or received any other COVID-19 vaccine.
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Participant with a history of hypersensitivity to any vaccine or a history of allergic disease or reactions likely to be exacerbated by any component of the MVC-COV1901.
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Body (oral, rectal, or ear) temperature ≥ 38.0°C or acute illness (not including minor illnesses such as diarrhea or mild upper respiratory tract infection at the discretion of the investigator) within 2 days before the first dose of study intervention.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description MVC-COV1901(S protein with adjuvant) MVC-COV1901(S protein with adjuvant) S-2P protein with CpG and Aluminum Hydroxide/0.5mL MVC-COV1901(Saline) MVC-COV1901(Saline) Saline/0.5 mL
- Primary Outcome Measures
Name Time Method Incidence of Adverse Event within 28 days post the second study intervention (Safety of MVC-COV1901) Day 1 to 28 days after second vaccination To evaluate the safety and tolerability of MVC-COV1901 from Visit 2 (Day 1) to Visit 7 (28 days after the second dose of study intervention) in terms of the number and percentage of participants with the occurrence of:
* Solicited local AEs (up to 7 days after each dose of study intervention)
* Solicited systemic AEs (up to 7 days after each dose of study intervention)
* Unsolicited AEs (up to 28 days after each dose of study intervention)
* AE of Special Interest (AESI)
* Vaccine-Associated Enhanced Disease(VAED)
* Serious adverse events (SAEs)Immunogenicity of MVC-COV1901 Day 1 to 28 days after second vaccination To evaluate the immunogenicity of MVC-COV1901, as compared to placebo, in terms of neutralizing antibody titers
- Secondary Outcome Measures
Name Time Method lot to lot consistency Day 1 to 28 days after second vaccination To evaluate the lot-to-lot consistency of MVC-COV1901 in participants of the ≥ 20 to \< 65 years age group, the equivalence of the neutralizing antibody Geometric Mean Titer(GMT) among 3 different lots of MVC-COV1901
Incidence of Adverse Event throughout study conduct (Safety of MVC-COV1901) Day 1 to 180 days after second vaccination To evaluate the safety of MVC-COV1901 over the study period in terms of the number and percentage of participants with the occurrence of:
* \>= Grade 3 AE
* AE of Special Interest (AESI)
* Vaccine-Associated Enhanced Disease(VAED)
* Serious adverse events (SAEs)
Trial Locations
- Locations (12)
Changhua Christian Hospital
🇨🇳Changhua, Taiwan
Tao-Yuan General Hospital
🇨🇳Taoyuan, Taiwan
National Cheng Kung University Hospital
🇨🇳Tainan, Taiwan
Taipei Medical University Hospital
🇨🇳Taipei, Taiwan
Kaohsiung Medical University Chung-Ho Memorial Hospital
🇨🇳Kaohsiung, Taiwan
China Medical University Hospital
🇨🇳Taichung, Taiwan
National Institute of Hygiene and Epidemiology
🇻🇳Hanoi, Vietnam
National Taiwan University Hospital
🇨🇳Taipei, Taiwan
Taipei Veteran General Hospital
🇨🇳Taipei, Taiwan
Tri-Service General Hospital
🇨🇳Taipei, Taiwan
Chang-Guang Memorial Hospital Lin-Kou
🇨🇳Taoyuan, Taiwan
Taipei Municipal Wan Fang Hospital
🇨🇳Taipei, Taiwan