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Clinical Trial Summary

A prospective, open-label and parallel non-randomized control trial and biomarker research study is intended to compare incidence of repeated COVID-19 infection, severe pneumonitis and mortality between lung cancer patients undergoing systemic antitumor therapies who get vaccinated with 1 booster dose(majorly against XBB) and those who refuse. Meanwhile, a biomarker research is designed to monitor serum level dynamics of specific antibodies against COVID-19,analyze its correlation with incidence of breakthrough infection and further explore optimal periods for vaccination.


Clinical Trial Description

A single booster dose will be administered depending on patients' willingness in the sixth month after symptomatic COVID-19 infection and status including repeated COVID19 infection, critical and/or severe conditions and all-cause death will be recorded during the next 6 months after vaccination or not. For antibody analysis, 5 ml blood samples will be collected from all of the included patients respectively in the 3rd ,4.5th and 6th months after latest occurrence of symptomatic infection and at the same timepoints after booster dose vaccination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06168032
Study type Interventional
Source Peking Union Medical College Hospital
Contact Mengzhao Wang, MD
Phone +8613911235467
Email mengzhaowang@sina.com
Status Recruiting
Phase N/A
Start date December 8, 2023
Completion date December 8, 2026

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