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XLCART001 Treatment in Relapsed/Refractory/High-risk B-cell Malignancy Subjects

5. august 2019 opdateret af: JianYong Li, The First Affiliated Hospital with Nanjing Medical University

A Single-center, Open Study Evaluating Efficacy and Safety of XLCART001(CD-19) Treatment in Relapsed/Refractory/High-risk B-cell Malignancy Subjects

The trial is a single arm, single-center, non-randomized clinical trial which is designed to evaluate the efficacy and safety of XLCART001 in treatment of relapsed/refractory/high-risk B-cell malignancy subjects

Studieoversigt

Status

Ukendt

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

10

Fase

  • Fase 2

Kontakter og lokationer

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

Studiesteder

    • Jiangsu
      • Nanjin, Jiangsu, Kina, 210029
        • Department of Haematology, the First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital

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 og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Age ≥18 years, male and female,
  • Confirmed as CD19-positive B cell lymphoma/leukemia by immunohistochemistry or flow cytometry
  • No effective treatment
  • Patients must have a measurable or evaluable disease at the time of enrollment.
  • Adequate organ system function including:

    • ALT/AST < 3 upper limit of normal; Total Bilirubin < 2.5 upper limit of normal
    • Creatinine < 2 upper limit of normal
    • Oxygen saturation ≥ 95%
    • Left ventricular ejection fraction ≥ 40%
    • Number of neutrophil ≥ 0.75×10^9/L, number of platelet ≥ 50×10^9/L
  • At least 4 weeks from receiving previous treatment (radiotherapy, chemotherapy, monoclonal antibody therapy or other treatments)
  • No contraindications of peripheral blood apheresis
  • Female subjects in childbearing age, their serum or urine pregnancy test must be negative. All patients must agree to take effective contraceptive measures during the trial measures
  • ECOG score 0-2, expected survival ≥ 12 weeks

Exclusion Criteria:

  • Women who are pregnant or lactating. Patients have breeding intent in 12 months or cannot take effective contraceptive measures during the trial measures
  • Uncontrollable active infection within four week. Prophylactic antibiotic, antiviral and antifungal treatment is permissible. Active hepatitis B or hepatitis C virus infection, as well as acquired, congenital immune deficiency diseases, including but not limited to HIV-infected persons
  • Subjects with any autoimmune disease or any immune deficiency disease
  • Have a history of allergy to antibodies or cellular products
  • Participated in any other clinical trial within four weeks
  • Used of systemic steroids within four weeks (using inhaled steroids or ≤ 20mg/d prednison are exceptions)
  • Have mental diseases
  • Have history of drug addiction
  • The investigators believe that any increase in the risk of the subject or interference with the results of the trial

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)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Overall response rate
Tidsramme: 12 weeks
Overall response rate (ORR) = complete response (CR) rate + partial response (PR) rate, ORR will be assessed at weeks 12.
12 weeks
Overall Survival
Tidsramme: 6 months,1 year, 2 years
from the time of enrollment to death from any cause or the date of the last follow-up visit
6 months,1 year, 2 years
Progression-free Survival
Tidsramme: 12 weeks,6 months,1 year, 2 years
the time from enrollment to disease progression, death from any cause, or the date of the last follow-up visit
12 weeks,6 months,1 year, 2 years
Event-free Survival
Tidsramme: 12 weeks,6 months,1 year, 2 years
the time from enrollment to any events, or the date of the last follow-up visit
12 weeks,6 months,1 year, 2 years

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Dose-limiting toxicity (DLT)
Tidsramme: 28 days
Non-haematological dose-limiting toxicities was any toxicity of grade 3 or higher occurring within 28 days of XLCART001 infusion judged possibly related to the treatment regimen.The following toxicities were not considered dose limiting toxicities: tumor lysis syndrome, abnormal electrolytes responding to supplementation, hypoalbuminemia, liver dysfunction resolving to ≤grade 2 within 14 days, transient (<72 hours) grade 4 hepatic enzyme abnormality, and grade 3 or 4 fever or neutropenic fever.
28 days
Number of CAR-T cells
Tidsramme: Day 1, Day 4, Day 7, Day 10, Day 14, Day 21, Day 28, 8 weeks, 12 weeks, 6 months, 1 years, 2 years
The number of CAR-T cells detected by flow cytometry and copy number of CAR-T cells tested by polymerase chain reaction
Day 1, Day 4, Day 7, Day 10, Day 14, Day 21, Day 28, 8 weeks, 12 weeks, 6 months, 1 years, 2 years
Duration of CAR-T cells
Tidsramme: Day 1, Day 4, Day 7, Day 10, Day 14, Day 21, Day 28, 8 weeks, 12 weeks, 6 months, 1 years, 2 years
The duration of CAR-T cells detected by flow cytometry and copy number of CAR-T cells tested by polymerase chain reaction
Day 1, Day 4, Day 7, Day 10, Day 14, Day 21, Day 28, 8 weeks, 12 weeks, 6 months, 1 years, 2 years

Samarbejdspartnere og efterforskere

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

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

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. juni 2018

Primær færdiggørelse (Forventet)

30. december 2019

Studieafslutning (Forventet)

1. juli 2020

Datoer for studieregistrering

Først indsendt

27. juni 2018

Først indsendt, der opfyldte QC-kriterier

14. juli 2018

Først opslået (Faktiske)

26. juli 2018

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

7. august 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

5. august 2019

Sidst verificeret

1. august 2019

Mere information

Begreber relateret til denne undersøgelse

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

produkt fremstillet i og eksporteret fra U.S.A.

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 .

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