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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

Studieoversikt

Status

Rekruttering

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Forventet)

25

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: CAR-NK019
All subjects were intravenously administrated with CAR-NK019
lentiviral vector-transducted HLA haploidentical NK cells to express anti-CD19 CAR
Andre navn:
  • CAR-NK019

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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
Tiltaksbeskrivelse
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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. mai 2021

Primær fullføring (Forventet)

1. mai 2022

Studiet fullført (Forventet)

1. mai 2024

Datoer for studieregistrering

Først innsendt

7. mai 2021

Først innsendt som oppfylte QC-kriteriene

13. mai 2021

Først lagt ut (Faktiske)

14. mai 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

14. mai 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

13. mai 2021

Sist bekreftet

1. mai 2021

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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