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NCT Number: NCT06503497

A Trail of Second-line Chemotherapy Sequential NKG2D CAR-NK Cell Therapy for Pancreatic Cancer

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

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

the first affiliated hospital of Zhejiang University,school of medicine

Hangzhou, Zhejiang, 310009, China

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Age between 18~75 years old (including boundary value), both male and female.
  • 2. Histologically or cytologically confirmed pancreatic ductal adenocarcinoma or IPMN carcinosis with at least first-line systemic therapy failure.
  • 3. Zubrod-ECOG-WHO score (see Annex 2) on a scale of 0-2.
  • 4. Life expectancy of at least 3 months at screening, as judged by the investigator.
  • 5. At least one stably evaluable target lesion according to RECIST1.1 criteria.
  • 6. Subject has adequate organ and bone marrow function. Laboratory screening results should be within the stable range described below, with no ongoing supportive care ("yellowing" therapy such as PTCD, ENBD, or bile duct stenting is allowed when pancreatic cancer invades the common bile duct).
  • 7. Remission of all toxicities due to prior antineoplastic therapy to Grade 0~1 (according to NCI CTCAE version 5.0) or to acceptable levels for inclusion/exclusion criteria.
  • 8. Childbearing status: not pregnant, and if of childbearing potential, willing to use effective contraception from the time of signing the informed consent form to 6 months after the last cell infusion (females of childbearing potential include premenopausal females and females within 2 years of postmenopause).
  • 9. Subjects must sign and date written informed consent.
  • 10. Subjects must be voluntary and able to comply with predetermined treatment regimens, laboratory tests, follow-up, and other study requirements.

Exclusion criteria

  • 1. Pregnant and lactating females.
  • 2. Positive serology for HIV, Treponema pallidum or HCV (those who are HCV antibody positive but HCV-RNA negative, stable syphilis and inactive patients can be included).
  • 3. Any active infection, including but not limited to active tuberculosis, HBV infection (including HBsAg positive, or HBcAb positive with HBV DNA above the lower limit of laboratory testing), Epstein-Barr virus (EBV) DNA positive, cytomegalovirus (CMV) DNA positive or novel coronavirus (new coronavirus) nucleic acid positive, and other bacterial, viral, or fungal infections requiring drug treatment;
  • 4. History of malignancy within 5 years, with the exception of basal cell carcinoma of the skin and carcinoma in situ of the cervix.
  • 5. Any other health condition that, in the judgment of the investigator, would preclude participation in the study.

Treatment and study plan

chemotherapy sequential CAR-NK cell infusion

Biological

In each chemotherapy cycle, patients received 2 intravenous infusions of CAR-NK on days 2 and 3 after each chemotherapy was discontinued.

Primary outcomes

  1. Maximum tolerated dose

    Time frame: within 28 days after NKG2D CAR-NK treatment

    Determine the optimal agent for NKG2D CAR-NK at maximum tolerated dose

  2. Dose limiting toxicity

    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

Secondary outcomes

  1. Effectiveness evaluation

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Zhejiang University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Jul 16, 2024
Registry last updated
Dec 27, 2024

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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