the first affiliated hospital of Zhejiang University,school of medicine
Hangzhou, Zhejiang, 310009, China
Location status: Recruiting
NCT Number: NCT06503497
This is a single-center, single-arm, open-label, dose-escalation clinical study to evaluate the safety and anti-tumor efficacy of second-line systemic chemotherapy sequential NKG2D CAR-NK cell therapy for pancreatic cancer
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Early Phase 1
Hangzhou, Zhejiang, 310009, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
In each chemotherapy cycle, patients received 2 intravenous infusions of CAR-NK on days 2 and 3 after each chemotherapy was discontinued.
Time frame: within 28 days after NKG2D CAR-NK treatment
Determine the optimal agent for NKG2D CAR-NK at maximum tolerated dose
Time frame: From enrollment of the first subject to completion of follow-up of the last subject up to 2 years
Describe the adverse events of limiting further increases in the dose of NKG2D CAR-NK
Time frame: At weeks 4、8 and months 3、6、9、12、16、20 and 24 after treatment
Objective Response Rate (ORR) According to Response Evaluation Criteria In Solid Tumors Version 1.1
Contact information is provided by the study sponsor or research team.
Zhejiang University
Other
A Single-center, Single-arm, Open-label, Dose-escalation Clinical Study to Evaluate the Safety and Anti-tumor Efficacy of Second-line Systemic Chemotherapy Sequential NKG2D CAR-NK Cell Therapy for Pancreatic Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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