Safety and Immunogenicity Study of Inactivated Vaccine for Prevention of SARS-CoV-2 Infection(COVID-19)
NCT04383574 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 422
Last updated 2022-08-11
Summary
This study is a randomized, double-blinded, and placebo controlled phase 1\&2 clinical trial of the SARS-CoV-2 inactivated vaccine manufactured by Sinovac Life Sciences Co. , Ltd. The purpose of this study is to evaluate the safety and immunogenicity of the experimental vaccine in healthy elderly aged 60 years and above.
Conditions
Interventions
- BIOLOGICAL
-
Two doses of medium dosage inactivated SARS-CoV-2 vaccine at the schedule of day 0,28
The inactivated SARS-CoV-2 vaccine was manufactured by Sinovac Research \& Development Co., Ltd..Two doses of medium dosage (600SU/0.5ml) experimental vaccine at the schedule of day 0,28,and one dose of booster immunization(the third dose) with medium dosage (600SU/0.5ml) experimental vaccine 1 year after primary immunization at the schedule of day 0,28 in phaseⅠand 6 months after primary immunization at the schedule of day 0,28 in phase Ⅱ.And the second booster dose (the fourth dose) 1 year after the second dose.
- BIOLOGICAL
-
Two doses of high dosage inactivated SARS-CoV-2 vaccine at the schedule of day 0,28
The inactivated SARS-CoV-2 vaccine was manufactured by Sinovac Research \& Development Co., Ltd..Two doses of high dosage (1200SU/0.5ml) experimental vaccine at the schedule of day 0,28,and one dose of booster immunization(the third dose) with medium dosage (1200SU/0.5ml) experimental vaccine 1 year after primary immunization at the schedule of day 0,28 in phaseⅠand 6 months after primary immunization at the schedule of day 0,28 in phase Ⅱ.And the second booster dose (the fourth dose) 1 year after the second dose.
- BIOLOGICAL
-
Two doses of placebo at the schedule of day 0,28
The placebo was manufactured by Sinovac Research \& Development Co., Ltd., Two doses of placebo at the schedule of day 0,28,and one dose of booster immunization with placebo 1 year after primary immunization at the schedule of day 0,28 in phaseⅠand 6 months after primary immunization at the schedule of day 0,28 in phase Ⅱ.
- BIOLOGICAL
-
Two doses of low dosage inactivated SARS-CoV-2 vaccine at the schedule of day 0,28
The inactivated SARS-CoV-2 vaccine was manufactured by Sinovac Research \& Development Co., Ltd..Two doses of low dosage (300SU/0.5ml)experimental vaccine at the schedule of day 0,28,and one dose of booster immunization with low dosage (300SU/0.5ml) experimental vaccine 6 months after primary immunization at the schedule of day 0,28 in phase Ⅱ.
Sponsors & Collaborators
-
Sinovac Life Sciences Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Yuliang Zhao, Master · Hubei Provincial Center for Disease Control and Prevention
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-05-22
- Primary Completion
- 2021-12-28
- Completion
- 2022-05-31
Countries
- China
Study Locations
More Related Trials
-
Efficacy and Safety of SA58 Nasal Spray in Close Contact With COVID-19 People
NCT05667714 ·Status: UNKNOWN ·Phase: NA
-
Evaluation of Corfluvec Vaccine for the Prevention of COVID-19 in Healthy Volunteers
NCT05696067 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Clinical Trial of COVID-19 Vaccine(SARS-CoV-2 Variant(Omicron BA.5) mRNA Vaccine) in Participants Aged 18 Years and Over
NCT05745545 ·Status: UNKNOWN ·Phase: NA
-
A Dose-Confirmation Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Vaccine CVnCoV in Healthy Adults for COVID-19
NCT04515147 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Evaluate Efficacy and Safety of "VIRACIDE" IN THE MANAGEMENT OF CORONA VIRUS DISEASE 2019 (COVID-19)
NCT04596085 ·Status: COMPLETED ·Phase: NA
-
A Study to Learn About The Study Medicine (Called PF-06823859) in Healthy Chinese Participants
NCT05257798 ·Status: COMPLETED ·Phase: PHASE1
-
A Trial of Remdesivir in Adults With Severe COVID-19
NCT04257656 ·Status: TERMINATED ·Phase: PHASE3
-
Study of VIR-2482 in Healthy Volunteers
NCT04033406 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess Safety, Tolerability, and Immunogenicity of V591 (COVID-19 Vaccine) in Healthy Participants (V591-001)
NCT04498247 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Dose-Confirmation Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1273 COVID-19 Vaccine in Adults Aged 18 Years and Older
NCT04405076 ·Status: COMPLETED ·Phase: PHASE2
-
Therapeutic Vaccine Trial of COVID-19 for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection
NCT04428073 ·Status: UNKNOWN ·Phase: PHASE1
-
Safety, Reactogenicity, and Immunogenicity Trial of CV2CoV mRNA Vaccine Against SARS-CoV-2 in Seropositive Adult Participants
NCT05260437 ·Status: COMPLETED ·Phase: PHASE1
-
Nitazoxanide Therapy for Patients With COVID-19 Pneumonia
NCT04561219 ·Status: COMPLETED ·Phase: PHASE2
-
COVidIVERmectin: Ivermectin for Treatment of Covid-19
NCT04438850 ·Status: TERMINATED ·Phase: PHASE2
-
A Study to Assess the Safety, Tolerability and Preliminary Efficacy of HH-120 for the Treatment of COVID-19
NCT06039163 ·Status: COMPLETED ·Phase: PHASE1
-
Clinical Trial to "Study the Efficacy and Therapeutic Safety of Ivermectin: (SAINTBO)
NCT04836299 ·Status: UNKNOWN ·Phase: PHASE2
-
New Antiviral Drugs for Treatment of COVID-19
NCT04392427 ·Status: UNKNOWN ·Phase: PHASE3
-
Safety, Tolerability, Pharmacokinetics, and Food Effect Study of RV299 in Healthy Adults
NCT06033612 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19
NCT04343651 ·Status: COMPLETED ·Phase: PHASE2
-
The Efficacy and Safety of Pyramax in Mild to Moderate COVID-19 Patients
NCT04475107 ·Status: COMPLETED ·Phase: PHASE2
-
Multicenter Randomized Double-blind Placebo-controlled Study to Investigate Azvudine in Symptomatic Adults With COVID-19 at Increased Risk of Progressing to Severe Illness
NCT05689034 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
Phase 2b/3 Trial of NuSepin® in COVID-19 Pneumonia Patients
NCT05352347 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
A Study to Learn About the Study Medicine Paxlovid (Nirmatrelvir + Ritonavir) in Adults Aged 60 and Older Living in Korean Long-term Care Hospitals Who Have COVID-19
NCT07089680 ·Status: NOT_YET_RECRUITING
-
Efficacy of Ivermectin in Outpatients With Non-severe COVID-19
NCT04834115 ·Status: UNKNOWN ·Phase: PHASE3
-
Efficacy and Safety of Molnupiravir (MK-4482) in Non-Hospitalized Adult Participants With COVID-19 (MK-4482-002)
NCT04575597 ·Status: COMPLETED ·Phase: PHASE2/PHASE3