Safety and Immunogenicity of COVID-19 Vaccine Administered in Older Adults

Older Adults Clinical Trial

Official title:

Safety and Immunogenicity of COVID-19 Vaccine Administered in Older Adults: A Multicenter Prospective Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05012800
• Other study ID #: ky-2021-7-7-1
• Status: Recruiting
• Phase: Phase 4
• Start date: July 28, 2021
• Est. completion date: September 30, 2022

Study information

• Verified date: July 2021
• Source: Beijing 302 Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The COVID-19 pandemic is causing unprecedented morbidity and mortality.The safe and effective Novel coronavirus vaccine is an effective means to block the transmission of the virus by building up the immune barrier of the population.Clinical studies have shown that elderly people are at high risk of severe COVID-19 infection and have poor clinical prognosis.Considering the current situation of aging population in China, the elderly people should be given priority to vaccinate to obtain protection and reduce the risk of novel coronavirus infection.However, the current data on vaccines are mostly from young and middle-aged healthy people, while there is little research data on COVID-19 vaccination in the elderly.This study mainly studied the safety and effectiveness of COVID-19 vaccine in the elderly population and explored its potential immune mechanism.

Description:

This study is a prospective, multicenter, controlled , open-label and phase I clinical trial. Older adults in the study included healthy people between the ages of 60 and 80 group. Those who is in line with the inclusion criteria and who is not in conformity with the exclusion criteria received two doses of COVID-19 vaccine at 0 days (baseline) and 21 days, respectively, and were followed up at 1, 3, 6, 9 and 12 months after completion of vaccination.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: September 30, 2022
• Est. primary completion date: August 31, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• A COVID-19 vaccine is planned.
• Older adults subjects aged 60-80 years or young adults subjects aged 18-59 years.
• Able and willing to follow the requirements of the clinical trial protocol and complete the study follow-up for 12 months.
• HBsAg, anti-HCV, HIV and TPHA were negative.
• Body temperature =37.0?.

Exclusion Criteria:

• People who are allergic to any component of the vaccine, or have a serious history of vaccine allergy.
• Women who is pregnant, breastfeeding, or planning to be pregnant within 6 months.
• Sufferring serious cardiovascular diseases, such as arrhythmia, conduction block, myocardial infarction, and severe hypertension can not be well controlled by drugs.
• Patients with severe chronic diseases or diseases can not be controlled well during the progress, such as asthma, diabetes, thyroid disease, etc.
• Patients with congenital or acquired angioedema / neuroedema.
• Patients with lymphoma, leukemia and other systemic malignancies.
• Patients with convulsions, epilepsy, encephalopathy, psychiatric disorders and other progressive neurological disorders, or a family history of them.
• Patients with acute attack of chronic diseases.
• During vaccination, immunomodulators, systemic cytotoxic drugs, immune checkpoint inhibitors (PD-1 / PDL-1 / CTLA-4, etc.) and cell therapy, including NK cells, cytokine induced killer cells, Dendritic cells, CTL and Stem cells infusion are required.
• Other conditions determined by the researcher.

Related Conditions & MeSH terms

• COVID-19 Vaccine
• Older Adults

Intervention

Biological:
• COVID-19 Vaccine
Coronavirus vaccine was inoculated on day 0 and day 21, respectively.

Locations

Country	Name	City	State
China	302 Hospital	Beijing

Sponsors (2)

Lead Sponsor	Collaborator
Beijing 302 Hospital	People's Hospital of Hunyuan County, Shanxi Province

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety of coronavirus vaccine	Recorded the adverse effects after COVID-19 vaccination	Within 2 months after the first dose of coronavirus vaccine
Primary	Immunogenicity of coronavirus vaccine	Detected the dynamics and titers of anti-SARS-CoV-2 antibodies	Within 2 months after the first dose of coronavirus vaccine
Secondary	Safety of coronavirus vaccine	Recorded the adverse effects after COVID-19 vaccination	Through study completion, an average of 13 months
Secondary	Immunogenicity	Detected the dynamics and titers of anti-SARS-CoV-2 antibodies	Through study completion, an average of 13 months