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The prospective clinical study for EBV-specific T cell treating EBV-associated lymphomas

The prospective clinical study for EBV-specific T cell treating EBV-associated lymphomas

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026323
Enrollment
Unknown
Registered
2019-09-29
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

EBV-associated lymphomas

Interventions

EBV-specific T cell treatment group:Infusing EBV-specific T cell

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) aged at least 14 years, gender not limited. (2) EBV-associated lymphoma confirmed by histopathological examination (virus nucleic acid testing or immunohistochemistry). (3) relapsed or refractoy EBV-associated lymphoma. (4) the presence of at least one measurable lesion. (5) the Eastern Cooperative Oncology Group (ECOG) scale of performance status is 0-2, estimated survival time is more than 3 weeks. (6) patients agree to participate in the study and sign informed consent

Exclusion criteria

Exclusion criteria: The subject should be excluded if any criterion listed below is met. (1) the central nervous system is involved. (2) a medical history of severe heart disease, including ventricular tachycardia, atrial fibrillation, cardiac block, myocardial infarction within one year, congestive heart failure and coronary heart disease with symptoms requiring medications. (3) renal insufficiency ( serum creatinine >180µmol/L) and/or liver insufficiency (total bilirubin >34 µmol/L, ALT/AST >3 times above the upper limit of normal). (4) participation in any other clinical trial within the last one month. (5) the participation is considered not suitable by the researchers.

Design outcomes

Primary

MeasureTime frame
The safety;

Secondary

MeasureTime frame
Overall response rate;Complete remission rate;Partial remission rate;Progression-free survival;Overall survival;

Countries

China

Contacts

Public ContactRuixiang Xia

Department of Hematology, the First Affiliated Hospital of Anhui Medical University

xrx2041@163.com+86 0551-62922041

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026