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Cluster-targeted specific multi-target cell cytotoxicity T lymphocyte technology in the individualized diagnosis and treatment strategy of recurrent/metastatic nasopharyngeal carcinoma.

Cluster-targeted specific multi-target cell cytotoxicity T lymphocyte technology in the individualized diagnosis and treatment strategy of recurrent/metastatic nasopharyngeal carcinoma.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082453
Enrollment
Unknown
Registered
2024-03-29
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

recurrent/metastatic nasopharyngeal carcinoma

Interventions

Test group:Gemcitabine + Cisplatin + PD-1 monoclonal antibody + CTL

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age =18 years, gender not specified; (2) Patients with initially treated recurrent metastatic nasopharyngeal carcinoma confirmed by pathological tissue and/or clinical examination; (3) Good physical condition: Karnofsky Performance Score (KPS) =70 points; (4) Expected survival =12 weeks; (5) No treatment that may affect efficacy evaluation has been received in the past month; (6) Normal hematopoietic and organ function; (7) Women of childbearing age who need to undergo serum pregnancy testing; patients must test negative in the serum test; (8) Participants voluntarily join this study and sign an informed consent form

Exclusion criteria

Exclusion criteria: (1) Patients currently participating in other clinical trials; (2) Patients who have a history of severe anaphylactic reactions, allergic reactions, or other allergic reactions to chimeric or humanized antibodies or fusion proteins, or who have an allergic constitution; (3) Patients with fever for various reasons, excluding transient fever caused by cell infusion; (4) Patients with active autoimmune diseases or a history of autoimmune diseases or related symptoms requiring systemic corticosteroid or immunosuppressive therapy.

Design outcomes

Primary

MeasureTime frame
Accuracy of diagnosis;Progression-free survival;

Secondary

MeasureTime frame
Objective response rate;Duration of response;Overall survival;

Countries

China

Contacts

Public ContactLei Liu

West China Hospital, Sichuan University

13882713780@163.com+86 188 0505 3037

Outcome results

None listed

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