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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05949749
Other study ID # SYSKY-2023-631-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 25, 2023
Est. completion date September 30, 2024

Study information

Verified date September 2023
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact Xiang-Wei Kong, Ph.D.
Phone 0086-020-34071439
Email sorahick@qq.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Epstein-barr virus (EBV) infection is a necessary factor of nasopharyngeal carcinoma (NPC). The incidence of NPC in endemic regions reaches 24.60/100,000 people, far higher than that of the worldwide average. However, no EBV prophylactic vaccines is clinically available so far, which is largely hampered by the difficulties in selecting optimal vaccine design target out of 13 glycoproteins on the surface of EBV. In this study, we utilized humanized gp42-IgG antibodies to explore the dominant epitopes of gp42, one of the functional EBV glycoproteins during virus entry, to facilitate prophylactic vaccine design.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date September 30, 2024
Est. primary completion date August 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Controls underwent physical examinations or primary NPC cases confirmed by pathology or cytology. - If cases, at stage I-IVB diagnosed by radiology according to AJCC/UICC 8th. - If cases, Karnofsky score (KFS)=70, estimated survival span>12 months. - If cases, no disordered of major organs is found; blood test, liver, and kidney functions are basically normal. - If cases, at least one measurable lesion according to Response Evaluation Criteria in Solid Tumours (RECIST) 1.1. Exclusion Criteria: - History of other malignant diseases. - History of severe systemic diseases or heart, lung, liver, or kidney disfunction. - History of severe neurological, metal, endocrine diseases. - History of HBV, HCV, HIV, TP, or TB infection. - If controls, physical examination reveals systemic diseases including malignant diseases. - If cases, incomplete blood and pathological sample data. - If cases, not receiving primary treatment in this facility. - Other individuals investigators find not suitable for the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Epitope exploration
Explore the epitope landscape of gp42-IgG of cases in comparison with that of controls.

Locations

Country Name City State
China Sun Yat-sen Memorial Hospital Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dominant gp42-IgG epitopes in cases Dominant gp42-IgG epitopes revealed by ELISA with non-competitive monoclonal humanized antibodies against gp42 will be compared between cases and controls. Baseline
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