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Trial record 1 of 1 for:    ZUMA-4
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Study Evaluating KTE-X19 in Pediatric and Adolescent Participants With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia or Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma (ZUMA-4)

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ClinicalTrials.gov Identifier: NCT02625480
Recruitment Status : Recruiting
First Posted : December 9, 2015
Last Update Posted : February 26, 2020
Sponsor:
Information provided by (Responsible Party):
Gilead Sciences ( Kite, A Gilead Company )

Brief Summary:
The primary objectives of this study are to evaluate the safety and efficacy of KTE-X19 in pediatric and adolescent participants with relapsed/refractory (r/r) B-precursor acute lymphoblastic leukemia (ALL) or relapsed or refractory (r/r) B-cell non-Hodgkin lymphoma (NHL).

Condition or disease Intervention/treatment Phase
Acute Lymphoblastic Leukemia Relapsed Non Hodgkin Lymphoma Refractory Non-Hodgkin Lymphoma Biological: KTE-X19 Drug: Fludarabine Drug: Cyclophosphamide Phase 1 Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 116 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1/2 Multi-Center Study Evaluating the Safety and Efficacy of KTE-X19 in Pediatric and Adolescent Subjects With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia or Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma (ZUMA-4)
Actual Study Start Date : February 1, 2016
Estimated Primary Completion Date : July 2021
Estimated Study Completion Date : January 2036


Arm Intervention/treatment
Experimental: Single Arm
A conditioning chemotherapy regimen of fludarabine and cyclophosphamide will be administered followed by a single infusion of CAR transduced autologous T cells administered intravenously at a target dose of 2 x 10^6 anti-CD19 CAR+ T cells/kg or 1 x 10^6 anti-CD19 CAR+ T cells/kg
Biological: KTE-X19
Drug: Fludarabine
Administered intravenously

Drug: Cyclophosphamide
Administered intravenously




Primary Outcome Measures :
  1. Phase 1: Percentage of Participants Experiencing Adverse Events Defined as Dose-Limiting Toxicities (DLT) [ Time Frame: Up to 28 days ]
    Dose-limiting toxicity is defined as protocol-defined KTE-X19-related events with onset within the first 28 days following KTE-X19 infusion.

  2. Phase 2: Overall Complete Remission Rate in the ALL Cohort [ Time Frame: Up to 24 months ]
    Overall complete remission rate will be determined per independent review.

  3. Phase 2: Objective Response Rate in the NHL Cohorts [ Time Frame: Up to 24 months ]
    Objective Response Rate will be determined per investigator review.


Secondary Outcome Measures :
  1. Minimum Residual Disease Negative Remission Rate in the ALL Cohort [ Time Frame: Up to 3 months ]
    Minimal residual disease (MRD) response rate is defined as MRD < 10^-4 per the standard assessment.

  2. Allogeneic Stem Cell Transplant Rate in the ALL Cohort [ Time Frame: Up to 24 months ]
    The incidence of allogeneic stem cell transplant will be analyzed.

  3. Changes Over Time in PRO Scores in the ALL Cohort [ Time Frame: Up to 15 years ]
  4. Overall Complete Remission Rate in the ALL Cohort [ Time Frame: Up to 15 years ]
  5. Relapse-Free Survival for the ALL Cohort [ Time Frame: Up to 24 months ]
    Relapse-Free Survival is defined as the time from the KTE-X19 infusion date to the date of disease relapse or death from any cause.

  6. Progression Free Survival in the NHL Cohort [ Time Frame: Up to 15 years ]
  7. Overall Survival in the ALL and NHL Cohorts [ Time Frame: Up to 15 years ]
    Overall survival is defined as the time from KTE-X19 infusion to the date of death from any cause.

  8. Duration of Remission in the ALL and NHL Cohorts [ Time Frame: Up to 24 months ]
    Duration of remission is defined as the time between the participant's first complete response per independent review to relapse or any death in the absence of documented relapse.

  9. Percentage of Participants with Anti-KTE-X19 Antibodies in Blood in the ALL and NHL Cohorts [ Time Frame: Up to 15 years ]
  10. Percentage of Participants Experiencing Adverse Events and Common Terminology Criteria for Adverse Events (CTCAE) Grade Changes in Safety Laboratory Values in ALL and NHL Cohorts [ Time Frame: Up to 15 years ]


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Ages Eligible for Study:   up to 21 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Key Inclusion Criteria for the ALL Cohort

  • Relapsed or refractory B-precursor ALL defined as one of the following:

    • Primary refractory disease
    • Relapsed or refractory disease after 2 or more lines of systemic therapy
    • Relapsed or refractory disease after allogeneic transplant provided individual is at least 100 days from stem cell transplant at the time of enrollment
  • Morphological disease in the bone marrow (> 5% blasts)
  • Individuals with Ph+ disease are eligible if they are intolerant to tyrosine kinase inhibitor (TKI) therapy, or if they have relapsed/refractory disease despite treatment with at least 2 different TKIs
  • Age ≤ 21 years and weight ≥ 6 kg at the time of assent or consent per IRB guidelines
  • Lansky (age < 16 years at the time of assent/consent) or Karnofsky (age ≥ 16 years at the time of assent/consent) performance status ≥ 80 at screening
  • Adequate renal, hepatic, pulmonary and cardiac function defined as:

    • Creatinine clearance ≥ 60 cc/min
    • Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≤ 5 x upper limit of normal (ULN)
    • Total bilirubin ≤ 1.5 x ULN, except in individuals with Gilbert's syndrome
    • Left ventricular shortening fraction (LVSF) ≥ 30% or left ventricular ejection fraction (LVEF) ≥ 50%, as determined by an echocardiogram or multi-gated acquisition scan (MUGA), no evidence of pericardial effusion (except trace or physiological) as determined by an ECHO and no clinically significant arrhythmias
    • No clinically significant pleural effusion
    • Baseline oxygen saturation > 92% on room air

Key Exclusion Criteria for the ALL Cohort

  • Diagnosis of Burkitt's leukemia/lymphoma according to the World Health Organization (WHO) classification or chronic myelogenous leukemia lymphoid blast crisis
  • History of malignancy other than non-melanoma skin cancer or carcinoma in situ (e.g. cervix, bladder, breast) unless disease free for at least 3 years
  • History of severe hypersensitivity reaction to aminoglycosides or any of the agents used in this study
  • Presence of central nervous system (CNS)-3 disease and CNS-2 disease with neurological changes
  • History of concomitant genetic syndrome such as Fanconi anemia, Kostmann syndrome, Shwachman-Diamond syndrome or any other known bone marrow failure syndrome
  • History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, or other clinically significant cardiac disease within 12 months of enrollment
  • History of symptomatic deep vein thrombosis or pulmonary embolism within 6 months of enrollment.
  • Primary immunodeficiency
  • Known infection with HIV, hepatitis B (HBsAg positive) or hepatitis C virus (anti-HCV positive)
  • Presence of fungal, bacterial, viral, or other infection that is uncontrolled or requiring IV antimicrobials for management.
  • Prior medication:

    • Prior CD19 directed therapy, including CAR+ T cell, BiTE, and antibody drug conjugate (ADC), with the exception of individuals who received KTE-X19 in this study and are eligible for re-treatment • Treatment with alemtuzumab within 6 months prior to leukapheresis, or treatment with clofarabine or cladribine within 3 months prior to leukapheresis
    • Donor lymphocyte infusion (DLI) within 28 days prior to enrollment
    • Any drug used for graft-versus-host disease (GVHD) within 4 weeks prior to enrollment
  • Acute GVHD grade II-IV by Glucksberg criteria or severity B-D by IBMTR index; acute or chronic GVHD requiring systemic treatment within 4 weeks prior to enrollment
  • Live vaccine ≤ 4 weeks prior to enrollment
  • Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the preparative chemotherapy on the fetus or infant. Females who have undergone surgical sterilization are not considered to be of childbearing potential
  • Individuals of both genders of child-bearing potential who are not willing to practice birth control from the time of consent through 6 months after the completion of KTE-X19

Key Inclusion Criteria for the NHL Cohort

  • Histologically confirmed aggressive B cell NHL
  • Relapsed or refractory histologically confirmed aggressive B-cell NHL per 1 or more of the following:

    • Primary refractory disease
    • Relapsed or refractory disease after 2 or more lines of systemic therapy
    • Relapsed or refractory disease after autologous /allogeneic transplant provided subject is at least 100 days from stem cell transplant at the time of enrollment
  • Individuals must have received adequate prior therapy including at a minimum all of the following:

    • Anti-CD20 monoclonal antibody, unless the investigator determines that the tumor is CD20 negative
    • An anthracycline-containing chemotherapy regimen
  • Age <18 years old and weight ≥ 6kg
  • Lansky (age < 16 years at the time of assent/consent) or Karnofsky (age ≥ 16 years at the time of assent/consent) performance status ≥ 80 at screening
  • Adequate renal, hepatic, pulmonary, and cardiac function defined as the following:

    • Creatinine clearance (as estimated by Cockcroft Gault or Schwartz) ≥ 60 cc/min
    • Serum ALT/AST ≤ 5 ULN
    • Total bilirubin ≤1.5 x ULN except in individuals with Gilbert's syndrome
    • Left ventricular shortening fraction(LVSF) ≥ 30% or left ventricular ejection fraction (LVEF)≥50%, as determined by ECHO or MUGA, no evidence of pericardial effusion (except trace or physiological) as determined by an ECHO, and no clinically significant arrhythmias
    • Baseline oxygen saturation > 92% on room air

Key Exclusion Criteria for the NHL Cohort

  • History of malignancy other than nonmelanoma skin cancer, carcinoma in situ (eg, cervix, breast), or FL unless disease free for at least 3 years
  • Prior CD19 targeted therapy other than blinatumomab
  • History of severe, immediate hypersensitivity reaction attributed to aminoglycosides
  • History of HIV infection or acute /chronic hepatitis B or C infection. Individuals with a history of hepatitis infection must have cleared their infection as determined by standard serological and genetic testing per current Infectious Diseases Society of America guidelines or applicable country guidelines
  • CNS abnormalities

    • Presence of CNS-3 disease, defined as detectable cerebrospinal blast cells in a sample of CSF with ≥ 5 WBCs per mm3 with or without neurological changes or presence of CNS-2 disease with neurological symptoms (see note below for further clarification), defined as detectable cerebrospinal blast cells in a sample of CSF with < 5 WBCs per mm^3 with neurological changes

      • Note: Individuals with CNS-1 (no detectable blast cells in the CSF) and those with CNS-2 without clinically evident ne urological changes are eligible to participate in the study.
    • History or presence of any CNS disorder such as a seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, any autoimmune disease with CNS involvement, posterior reversible encephalopathy syndrome (PRES), or cerebral edema
  • History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, or other clinically significant cardiac disease within 12 months of enrollment
  • Primary immunodeficiency
  • History of severe immediate hypersensitivity reaction to any of the agents used in this study
  • Live vaccine ≤ 6 weeks prior to planned start of conditioning regimen
  • Individuals of both genders who are not willing to practice birth control from the time of consent through 6 months after the completion of conditioning chemotherapy

Note: Other protocol defined Inclusion/Exclusion criteria may apply.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02625480


Contacts
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Contact: Medical Information 1-844-454-5483(1-844-454-KITE) medinfo@kitepharma.com

Locations
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Sponsors and Collaborators
Kite, A Gilead Company
Investigators
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Study Director: Kite Study Director Kite, A Gilead Company

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Responsible Party: Kite, A Gilead Company
ClinicalTrials.gov Identifier: NCT02625480    
Other Study ID Numbers: KTE-C19-104
2015-005010-30 ( EudraCT Number )
First Posted: December 9, 2015    Key Record Dates
Last Update Posted: February 26, 2020
Last Verified: February 2020

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Lymphoma
Leukemia
Lymphoma, Non-Hodgkin
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Lymphoid
Lymphoma, B-Cell
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Cyclophosphamide
Fludarabine
Fludarabine phosphate
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Antirheumatic Agents
Antineoplastic Agents, Alkylating
Alkylating Agents
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Myeloablative Agonists
Antimetabolites, Antineoplastic
Antimetabolites