Clinical trial · Interventional
Treatment of Malignant Tumors With Antigen Peptide-specific DC-CTL Cells and Decitabine
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Tumor-specific antigens can be induced by demethylation drugs. Antigen-targeting DC-CTL cells supposed to eliminate cancer cells efficiently and specifically. In this study investigators co-culture DCs cells with peptides derived from tumor specific antigen to generate antigen-specific DC-CTLs (Ag-CTL). Following treatment with demethylation drugs, Ag-CTL will be used to eliminate tumor cells. This study aims to evaluate the effectiveness and safety of Ag-CTL combined with demethylation drugs.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Malignant Tumor | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| DC-CTL | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment
- description
- DAC combined with Ag-CTL
- interventionNames
- Biological: DC-CTL
Primary outcomes (1)
- measure
- PFS
- timeFrame
- From date of initial treatment until the date of first documented progression, assessed up to 36 months.
- description
- progression free survival time
Secondary outcomes (1)
- measure
- OS
- timeFrame
- From date of diagnosis until the end of the follow-up, assessed up to 36 months.
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Male or female patients aged 18-70 (including 18 and 70 years old); 2. Diagnosed as malignant tumor by pathological and histological examination; 3. Patients with ECOG score \<2 and estimated survival time\>3 months; 4. Patients need to receive systemic combined chemotherapy according to their condition; other treatments such as surgery, radiotherapy, and targeted therapy are excluded; 5. The previous treatment-related toxicity of the patient 2 weeks before the enrollment had returned to \<1 grade at the time of enrollment (except for low-grade toxicity such as alopecia and peripheral neuritis); 6. The patient's intravenous access is unobstructed, which can meet the needs of intravenous drip; 7. The patient voluntarily participates and signs the informed consent form, and follows the research treatment plan and visit plan; Exclusion Criteria: * Any one of the exclusion criteria shall not be included in the group: 1. Patients used high-dose hormones within 1 week before enrollment (except for patients using inhaled hormones) 2. People with severe autoimmune diseases, immunodeficiency diseases or severe allergies; 3. Patients treated with other cellular immune products (DC, T, NK, and CAR-T, etc.); 4. The patient had uncontrollable infections within 4 weeks before enrollment; 5. Active HBV DNA\>1000copy/mL/C hepatitis (anti-HCV positive, HCV RNA positive), HIV positive, syphilis positive; 6. The patient participated in other clinical studies within 6 weeks before enrollment; 7. Patients suffering from mental illness; 8. The patient has drug abuse/addiction and medical, psychological or social conditions that may interfere with research or have an impact on the evaluation of research results; 9. The patient has alcohol dependence; 10. Women who are pregnant (positive urine/blood pregnancy studies) or breastfeeding; men or women who have a pregnancy plan within the past year; patients cannot be guaranteed to take effective contraceptive measures during the study period; 11. According to the judgment of the investigator, the patient has other unsuitable conditions for enrollment.
References
Publications (0)
Data not yet available