Clinical trial · Interventional
Immunotherapy of CD8+NKG2D+ AKT Cell With Chemotherapy to Pancreatic Cancer
A Randomized, Double Blinding, Placebo-Controlled Clinical Trials of CD8+NKG2D+ AKT Cell Immunotherapy to the Pancreatic Cancer Patients Treated With Adjuvant Chemotherapy
NCT02929797CI-TRIAL-00024226AKTunknownEarly Phase 1ClinicalTrials.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)
A Prospective Study on the Efficacy and Safety of CD8+NKG2D+ AKT cell immunotherapy to the pancreatic cancer patients treated with adjuvant chemotherapy.
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 |
|---|---|---|---|
| Pancreatic Ductal Adenocarcinoma | Pancreatic Ductal Adenocarcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CD8+NKG2D+ AKT Cell | Biological | — | UNRESOLVED |
| Gemcitabine | Drug | Gemcitabine | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- AKT + gemcitabine
- description
- gemcitabine dose 1000mg/M\^2, d1,8,15,q4w ×6 AKT 5\*10\^8/M\^2, d16,q4w ×6 Drug: gemcitabine Biological: AKT, CD8+NKG2D+ AKT Cell
- interventionNames
- Biological: CD8+NKG2D+ AKT Cell
- Drug: Gemcitabine
- type
- ACTIVE_COMPARATOR
- label
- gemcitabine
- description
- gemcitabine hydrochloride dose 1000mg/M2 d1,8,15,q4w ×6 Drug: gemcitabine
- interventionNames
- Drug: Gemcitabine
Primary outcomes (1)
- measure
- Disease-free survival
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * 1\. Diagnosed as stage II-III pancreatic ductal adenocarcinoma patients by pathologic histology; * 2\. Pancreatic cancer after radical resection; * 3\. Eastern Cooperative Oncology Group Performance Status less than 2; * 4\. Without radiotherapy or neoadjuvant chemotherapy; * 5\. The man or the gestation and lactation women Age between 18 to 80 years old; * 6\. Bone marrow functioned well: ANC more than 1.5\*10\^9/ L, PLT more than 100\*10\^9/LHgb more than 9 g/dL; * 7\. Blood biochemical indicators: AST(SGOT)less than 1.5 ULNALT(SGPT)less than 1.5 ULN, TBIL less than 1.5 ULN; * 8\. PT and PPT are in normal ranges; * 9\. Three months prior to clinical research did not receive any other clinical research trials; * 10\. patients are voluntary, and willing to sign informed consent. Exclusion Criteria: * 1\. Patients with other malignant tumors in the past five years; * 2\. Active viral or bacterial infection and cannot be controlled with appropriate anti-infection treatment; * 3\. Known as HIV infection, active hepatitis B virus or hepatitis C virus infection; * 4\. Known allergy to any kind of component of study drugs; * 5\. History of connective tissue disease(Such as lupus, scleroderma, nodular arteritis); * 6\. Patients with a history of interstitial pneumoniaSlowly progressive difficulty in breathing and hoose Sarcoidosissilicosis Fibrose pulmonaire idiopathiquehylactic pneumonia or A variety of allergy; * 7\. Suffering from mental illness or other illness, such as heart or lung disease, diabetes, etc. that can not be controlled, and can not cope with study treatment and monitoring requirements; * 8\. At the same time Patients participate in any other use of interventional medicine clinical research or checkers.
References
Publications (0)
Data not yet available
No reference posted for this study.