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Prospective study of TAC-T cells targeting Nectin4/NKG2DL (secreting IL7 and CCL21) combined with TAC-T cells targeting FAP (secreting IL12) in adjuvant treatment of advanced nasopharyngeal carcinoma and other solid tumors

Prospective study of TAC-T cells targeting Nectin4/NKG2DL (secreting IL7 and CCL21) combined with TAC-T cells targeting FAP (secreting IL12) in adjuvant treatment of advanced nasopharyngeal carcinoma and other solid tumors

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046032
Enrollment
Unknown
Registered
2021-05-02
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Nasopharyngeal carcinoma

Interventions

Experimental group:Intravenous reinfusion, local injection of TAC-T cells

Sponsors

Jinshazhou Hospital, Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years, there is no gender limit; 2. ECOG score 0-3; 3. Nectin4/NKG2DL and FAP positive (immunohistochemistry or flow cytometry); 4. Complete remission has not been achieved after the second-line treatment; disease progression occurs during any treatment, or the disease stable time is equal to or less than 6 months; or disease progression or recurrence within 12 months after autologous hematopoietic stem cell transplantation; 5. There is at least one measurable lesion, and any long diameter of the lesion is required to be greater than 0.5cm, and the lesion on the PET-CT scan is ingested; 6. The absolute value of peripheral blood neutrophils >= 1000/µl, platelets >= 45,000/µl; 7. Heart, liver and kidney function: creatinine = 50%; 8. Have sufficient understanding ability and voluntarily sign the informed consent form; 9. Reproductive patients must be willing to use contraceptive methods.

Exclusion criteria

Exclusion criteria: 1. Have autologous hematopoietic stem cell transplantation within 6 weeks; 2. Received cytotoxic drugs, glucocorticoids and other targeted drugs within 2 weeks before cell collection; 3. Active autoimmune diseases; 4. Active infection that cannot be controlled; 5. HIV infection, uncontrolled HBV, HCV, and syphilis infection; 6. Known central nervous system tumors.

Design outcomes

Primary

MeasureTime frame
Adverse events;Complete remission rate;Partial remission rate;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactLuo Rongcheng

Jinshazhou Hospital, Guangzhou University of Chinese Medicine

luorc02@vip.163.com+86 18826313419

Outcome results

None listed

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