Clinical trial · Observational
In Vitro Functional Modulation of Monocyte-derived Dendritic Cells of Patients With Cancer by Peptides
NCT02159937CI-TRIAL-00018758completedClinicalTrials.gov clinicaltrialsProvenance
- 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)
The purpose of this study is to evaluate in vitro the potential of peptides, to modify, phenotypically and functionally, the monocyte-derived dendritic cells of patients with metastatic cancer.
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 |
|---|---|---|---|
| Metastatic Cancer | Malignant Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood sampling by vena punction. | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Patients with metastatic cancer
- description
- Blood sampling by vena punction.
- interventionNames
- Other: Blood sampling by vena punction.
Primary outcomes (3)
- measure
- Expression of cellular markers in the dendritic cells (DCs) after stimulation with the peptides.
- timeFrame
- At the seventh day of the cells culture period
- measure
- Viability of the dendritic cells (DCs) after stimulation with the peptides.
- timeFrame
- At the seventh day of the cells culture period
- measure
- Cytokines production by the dendritic cells (DCs) after stimulation with the peptides.
- timeFrame
- At the seventh day of the cells culture period
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Signature of the Informed Consent Form before the performing of any procedures related to the study; 2. Age ≥18 years; 3. Histologically confirmed metastatic malignant neoplasia; 4. Results of laboratorial exams in the first 6 weeks before the blood sample collection within the following values: * White blood cells ≥ 3.000/μL; * Platelet count ≥ 100,000/mm³; * Hemoglobin \> 10g/dL; * Serum aspartate aminotransaminase (AST), alanine aminotransferase (ALT) and alkaline phosphatase \< 2.5 x upper limit of normal (ULN); * Serum creatinine \< 1.5 x upper limit of normal (ULN); 5. Karnofsky performance status ≥ 70%. Exclusion Criteria: 1. Presence of autoimmune disorders or conditions that require systemic treatment with immunosuppressant medications or systemic corticosteroids; 2. Received any systemic chemotherapy or radiotherapy within 15 days prior to the blood sample collection; 3. Received any immunotherapy within 4 weeks prior to the blood sample collection; 4. Known history of positive serology for HIV (human immunodeficiency virus).
References
Publications (0)
Data not yet available
No reference posted for this study.