Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Clinical Study of HLA Haploidentical CAR-NK Cells Targeting CD19 in the Treatment of Refractory/Relapsed B-cell NHL

To study the safety and effectiveness of HLA haploidentical CAR-NK cells targeting CD19 in patients with B-cell non-Hodgkin's lymphoma

Studieoversigt

Status

Rekruttering

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

25

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Zhejiang
      • Hangzhou, Zhejiang, Kina, 310009
        • Rekruttering
        • 2nd Affiliated Hospital, School of Medicine, Zhejiang University
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 75 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Volunteer to participate in this study and sign an informed consent form;
  2. Age 18-75 years old, no gender limit;
  3. Histologically diagnosed as diffuse large B-cell lymphoma (DLBCL), transforming follicular lymphoma (TFL), primary mediastinal B-cell lymphoma (PMBCL), mantle cell lymphoma (MCL) and other inert B-cells NHL conversion type:

    • Refractory or relapsed DLBCL refers to the failure to achieve complete remission after 2-line treatment; disease progression during any treatment, or disease stable time equal to or less than 6 months; or disease progression or recurrence within 12 months after autologous hematopoietic stem cell transplantation ;
    • Refractory or relapsed MCL must be resistant to or intolerable to BTK inhibitors;
    • Refractory or relapsed indolent B-cell NHL is the failure or recurrence of third-line treatment;
    • Previous treatment must include CD20 monoclonal antibody treatment (unless the subject is CD20 negative) and anthracyclines;
  4. At least one measurable lesion with the longest diameter ≥ 1.5 cm exists;
  5. The expected survival period is ≥12 weeks;
  6. The puncture section of the tumor tissue was positive for CD19 expression;
  7. ECOG score 0-2 points;
  8. Sufficient organ function reserve:

    • Alanine aminotransferase, aspartate aminotransferase ≤ 2.5× UNL (upper limit of normal value);
    • Creatinine clearance rate (Cockcroft-Gault method) ≥60 mL/min;
    • Serum total bilirubin and alkaline phosphatase ≤1.5× UNL;
    • Glomerular filtration rate>50Ml/min
    • Cardiac ejection fraction (EF) ≥50%;
    • Under natural indoor air environment, basic oxygen saturation>92%
  9. Allow a previous stem cell transplantation
  10. The approved anti-B-cell lymphoma treatments, such as systemic chemotherapy, systemic radiotherapy, and immunotherapy, have been completed for at least 3 weeks before the study medication;
  11. Allow patients who have previously received CAR-T cell therapy and have failed or relapsed after 3 months of evaluation;
  12. Female subjects of childbearing age must have a negative pregnancy test and agree to take effective contraceptive measures during the trial
  13. Two tests for the new coronavirus were negative.

Exclusion Criteria:

  1. Those who have a history of allergies to any of the ingredients in cell products;
  2. History of other tumors
  3. Previously presented with II-IV degree (Glucksberg criteria) acute GvHD or extensive chronic GvHD; or are receiving anti-GvHD treatment;
  4. Have received gene therapy in the past 3 months;
  5. Active infections that require treatment (except for simple urinary tract infections and bacterial pharyngitis), but preventive antibiotics, antiviral and antifungal infection treatments are allowed;
  6. Hepatitis B (HBsAg positive, but HBV-DNA <103 is not an exclusion criterion) or hepatitis C virus infection (including virus carriers), syphilis and other subjects with acquired and congenital immunodeficiency diseases, including But not limited to people living with HIV;
  7. According to the New York Heart Association's Heart Function Classification Standard, it is classified as Grade III or Grade IV.

    Impaired subjects;

  8. Those who have received anti-tumor therapy in the early stage but the toxic reaction has not recovered (the CTCAE 5.0 toxic reaction has not recovered to ≤1, except for fatigue, anorexia, and hair loss);
  9. Subjects with a history of epilepsy or other central nervous system diseases;
  10. Enhanced CT or MRI of the head showed evidence of central nervous system lymphoma;
  11. Have received any other drugs that target CD19;
  12. Women who are breastfeeding and unwilling to stop breastfeeding;
  13. Any other situation that the investigator believes may increase the risk of the subject or interfere with the results of the test.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: CAR-NK019
All subjects were intravenously administrated with CAR-NK019
lentiviral vector-transducted HLA haploidentical NK cells to express anti-CD19 CAR
Andre navne:
  • CAR-NK019

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Incidence of dose limiting toxicity (DLTs)
Tidsramme: Up to 28 days
To evaluate the safety, tolerability, and determine the recommended dosage of Anti-CD19 CAR-NK Cell Therapy for B-cell Non-Hodgkin Lymphoma
Up to 28 days
The overall response rate(ORR)
Tidsramme: Up to 2 years
To determine the anti-tumor effectivity of CAR-NK019
Up to 2 years

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Overall survival (OS)
Tidsramme: Up to 2 years
To determine the anti-tumor effectivity of CAR-NK019
Up to 2 years
progression free survival (PFS)
Tidsramme: Up to 2 years
To determine the anti-tumor effectivity of CAR-NK019
Up to 2 years
Pharmacokinetics of CAR positive cells
Tidsramme: Up to 2 years
The copy number of CAR DNA was measured at the preset follow-up time point.
Up to 2 years
Pharmacokinetics of CAR-NK cells
Tidsramme: Up to 2 years
The duration of CAR-positive NK cells in circulation was measured by FACs
Up to 2 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. maj 2021

Primær færdiggørelse (Forventet)

1. maj 2022

Studieafslutning (Forventet)

1. maj 2024

Datoer for studieregistrering

Først indsendt

7. maj 2021

Først indsendt, der opfyldte QC-kriterier

13. maj 2021

Først opslået (Faktiske)

14. maj 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

14. maj 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

13. maj 2021

Sidst verificeret

1. maj 2021

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med B-celle non-hodgkin lymfom

Kliniske forsøg med anti-CD19 CAR-NK

Abonner