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Study Evaluating the Safety and Efficacy of JCARH125 in Subjects With Relapsed and/or Refractory Multiple Myeloma (EVOLVE)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03430011
Recruitment Status : Recruiting
First Posted : February 12, 2018
Last Update Posted : May 4, 2020
Sponsor:
Information provided by (Responsible Party):
Juno Therapeutics, a Subsidiary of Celgene

Brief Summary:
This is an open-label, multicenter, Phase 1/2 study to determine the safety and efficacy of JCARH125, a CAR T-cell product that targets B-cell maturation antigen (BCMA), in adult subjects with relapsed and/or refractory multiple myeloma. The study will include a Phase 1 part to determine the recommended dose of JCARH125 in subjects with relapsed and/or refractory multiple myeloma, followed by a Phase 2 part to further evaluate the safety and efficacy of JCARH125 at the recommended dose. The safety and tolerability of JCARH125 in subjects who receive prophylactic treatment with anakinra will be evaluated in a separate Phase 1 cohort. The antitumor activity of JCARH125 in subjects who have been previously treated with BCMA-directed therapy will be evaluated in separate Phase 2a cohorts.

Condition or disease Intervention/treatment Phase
Multiple Myeloma Biological: JCARH125 Biological: JCARH125 + anakinra Phase 1 Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 245 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Protocol H125001: An Open-Label Phase 1/2 Study of JCARH125, BCMA-targeted Chimeric Antigen Receptor (CAR) T Cells, in Subjects With Relapsed or Refractory Multiple Myeloma
Actual Study Start Date : February 1, 2018
Estimated Primary Completion Date : March 2023
Estimated Study Completion Date : March 2023

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Multiple Myeloma
Drug Information available for: Anakinra

Arm Intervention/treatment
Experimental: JCARH125
Subjects will receive a course of lymphodepleting chemotherapy with fludarabine and cyclophosphamide followed by a single dose of JCARH125
Biological: JCARH125
Participants will undergo leukapheresis to isolate peripheral blood mononuclear cells (PBMCs) for the production of JCARH125. During JCARH125 production, participants may receive bridging chemotherapy for disease control. Following successful generation of JCARH125 product, participants will receive a course of lymphodepleting chemotherapy followed by one dose of JCARH125 administered intravenously (IV).

Experimental: JCARH125 + anakinra
Subjects will receive a course of lymphodepleting chemotherapy with fludarabine and cyclophosphamide followed by prophylactic treatment with anakinra and a single dose of JCARH125
Biological: JCARH125 + anakinra
Participants will undergo leukapheresis to isolate PBMCs for the production of JCARH125. During JCARH125 production, participants may receive bridging chemotherapy for disease control. Following successful generation of JCARH125 product, participants will receive a course of lymphodepleting chemotherapy followed by two doses of anakinra administered subcutaneously and one dose of JCARH125 administered IV. Subjects receive anakinra for 5 consecutive days following JCARH125 infusion.




Primary Outcome Measures :
  1. Phase 1: Incidence of dose-limiting toxicities (DLTs) [ Time Frame: 21 days ]
    Proportion of subjects with adverse events meeting DLT criteria

  2. Phase 1: Incidence and severity of adverse events [ Time Frame: 2 years ]
    Proportion of subjects with adverse events overall and by severity grade

  3. Phase 1: Incidence and severity of clinically significant laboratory abnormalities [ Time Frame: 2 years ]
    Proportion of subjects with clinically significant laboratory abnormalities overall and by severity grade

  4. Phase 1 Anakinra Cohort only: Incidence and severity of Grade 2 or higher cytokine release syndrome (CRS) [ Time Frame: 2 years ]
    Proportion of subjects with Grade 2 or higher CRS

  5. Phase 1 Anakinra Cohort only: Percentage of subjects with no CRS on Days 1, 2, or 3 following JCARH125 infusion [ Time Frame: 2 years ]
    Proportion of subjects with no CRS on Days 1, 2, or 3 following JCARH125 infusion

  6. Phase 1 Anakinra Cohort only: Time to onset of Grade 2 or higher CRS [ Time Frame: 2 years ]
    Median time to onset of Grade 2 or higher CRS

  7. Phase 2: Overall response rate [ Time Frame: 2 years ]
    Proportion of subjects with a partial response or better by International Myeloma Working Group (IMWG) criteria


Secondary Outcome Measures :
  1. Phase 1 and Phase 2: Maximum concentration (Cmax) of JCARH125 in the blood [ Time Frame: 2 years ]
  2. Phase 1 and Phase 2: Time to maximum concentration (Tmax) of JCARH125 in the blood [ Time Frame: 2 years ]
  3. Phase 1 and Phase 2: Area under the concentration vs time curve (AUC) of JCARH125 in the blood [ Time Frame: 2 years ]
  4. Phase 1 and Phase 2: Duration of persistence of JCARH125 CAR T cells in the blood [ Time Frame: 2 years ]
  5. Phase 1: Overall response rate [ Time Frame: 2 years ]
    Proportion of subjects with a partial response (PR) or better by IMWG criteria

  6. Phase 1 and Phase 2: Complete response (CR) rate [ Time Frame: 2 years ]
    Proportion of subjects with a CR by IMWG criteria

  7. Phase 2: Duration of response [ Time Frame: 2 years ]
    Time from first response (stringent complete response [sCR], CR, very good partial response [VGPR], or PR) to the earlier date of progressive disease (PD) or death due to any cause

  8. Phase 2: Duration of CR [ Time Frame: 2 years ]
    Time from first sCR or CR to the earlier date of PD or death due to any cause

  9. Phase 2: incidence and severity of adverse events [ Time Frame: 2 years ]
    Proportion of subjects with adverse events overall and by severity grade

  10. Phase 2: Incidence and severity of clinically significant laboratory abnormalities [ Time Frame: 2 years ]
    Proportion of subjects with clinically significant laboratory abnormalities overall and by severity grade

  11. Phase 2: Overall survival [ Time Frame: 2 years ]
    Time from JCARH125 infusion until death

  12. Phase 2: Progression-free survival [ Time Frame: 2 years ]
    Time from JCARH125 infusion until the earliest of date of death or disease progression as assessed by IMWG criteria

  13. Phase 2: Time to response [ Time Frame: 2 years ]
    Time from JCARH125 infusion to first documentation of PR or better

  14. Phase 2: Time to CR [ Time Frame: 2 years ]
    Time from JCARH125 infusion to first documentation of CR or better

  15. Phase 2 (excluding Phase 2a): Changes in measures of health-related quality of life (HRQoL) [ Time Frame: 2 years ]
    Change from baseline in HRQoL

  16. Phase 2 (excluding Phase 2a): Numbers of days in the intensive care unit (ICU) [ Time Frame: 2 years ]
  17. Phase 2 (excluding Phase 2a): Number of non-ICU inpatient days [ Time Frame: 2 years ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Key Inclusion Criteria:

  1. Diagnosis of multiple myeloma (MM) with relapsed and/or refractory (R/R) disease. Participants must have received at least 3 prior anti-myeloma treatment regimens. Participants must have previously received all of the following therapies and must be refractory to the last line of therapy prior to entering the study (not applicable to Phase 2a):

    1. Autologous stem cell transplant
    2. A regimen that included an immunomodulatory agent (eg, thalidomide, lenalidomide, pomalidomide) and a proteasome inhibitor (eg, bortezomib, carfilzomib, ixazomib), either alone or in combination
    3. Anti-CD38 (eg, daratumumab) as part of a combination regimen or as a monotherapy

    Subjects who have received prior allogeneic stem cell transplant or donor lymphocyte infusion at least 100 days before enrollment with no signs of acute or chronic graft-versus-host disease (GVHD) will be considered eligible. Subjects who were not candidates to receive one or more of the above treatments (ie, contraindicated) are eligible.

  2. Subjects must have measurable disease.
  3. Subject must be willing to provide fresh bone marrow biopsy samples during Screening (and prior to study treatment, if required).
  4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  5. Adequate renal, bone marrow, hepatic, pulmonary, and cardiac function
  6. Phase 2a cohorts only - Subjects with R/R MM who have been previously treated with prior BCMA-directed anti-myeloma therapy, achieved at least a partial response (PR) and progressed on the following treatment:

    1. Subjects who have received prior BCMA-directed CAR T-cell therapy. The last CAR T-cell therapy must have been received at least 6 months prior to JCARH125 screening.
    2. Subjects who have received prior BCMA-directed T-cell engager therapy.
    3. Subjects who have received prior BCMA-directed antibody-drug conjugate therapy.

Exclusion Criteria:

  1. Subjects with known active or history of CNS involvement by malignancy
  2. Subjects with solitary plasmacytoma; active or history of plasma cell leukemia (PCL); Waldenstrom's macroglobulinemia; Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal plasmaproliferative disorder, Skin changes (POEMS) syndrome; or symptomatic amyloidosis
  3. Subjects who are considered eligible to receive and have not refused an autologous stem cell transplant
  4. History of another primary malignancy that has not been in remission for at least 3 years. The following are exempt from the 3-year limit: non-melanoma skin cancer, curatively treated localized prostate cancer, cervical carcinoma in situ on biopsy or a squamous intraepithelial lesion on Pap smear, and in situ breast cancer that has been completely resected.
  5. Require systemic immunosuppressive therapies (eg, calcineurin inhibitors, methotrexate, mycophenolate, rapamycin, thalidomide, immunosuppressive antibodies such as anti-IL-6 or anti-IL-6 receptor [IL-6R])
  6. Prior CAR T-cell or other genetically-modified T-cell therapy (not applicable for subjects enrolled in Phase 2a cohorts)
  7. Prior treatment with a BCMA-targeted agent (not applicable for subjects enrolled in Phase 2a cohorts)
  8. History or presence of clinically relevant CNS pathology such as epilepsy, seizure, paresis, aphasia, stroke, severe brain injuries, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis
  9. Untreated or active infection at time of initial screening, at the time of leukapheresis, within 72 hrs before lymphodepletion, or 5 days before JCARH125 infusion.
  10. History of any of the following cardiovascular conditions within 6 months of screening: Class III or IV heart failure as defined by the New York Heart Association (NYHA), myocardial infarction, unstable angina, uncontrolled or symptomatic atrial arrhythmias, any ventricular arrhythmias, or other clinically significant cardiac disease
  11. Subjects with known hypersensitivity to E Coli-derived proteins (only applicable to subjects in Phase 1 Anakinra Cohort)
  12. History of severe immediate hypersensitivity reaction to any of the protocol-mandated or recommended agents used in this study

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): NCT03430011


Contacts
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Contact: H125001 Medical Monitor 732-540-0022 medical.monitorH125@celgene.com

Locations
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Sponsors and Collaborators
Juno Therapeutics, a Subsidiary of Celgene
Investigators
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Study Director: Mariana Cota, MD Juno Therapeutics, Inc.
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Responsible Party: Juno Therapeutics, a Subsidiary of Celgene
ClinicalTrials.gov Identifier: NCT03430011    
Other Study ID Numbers: H125001
First Posted: February 12, 2018    Key Record Dates
Last Update Posted: May 4, 2020
Last Verified: April 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Juno Therapeutics, a Subsidiary of Celgene:
JCARH125
chimeric antigen receptor
multiple myeloma
CAR T cells
B-cell maturation antigen
BCMA
autologous T-cell therapy
immunotherapy
Additional relevant MeSH terms:
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Multiple Myeloma
Neoplasms, Plasma Cell
Neoplasms by Histologic Type
Neoplasms
Hemostatic Disorders
Vascular Diseases
Cardiovascular Diseases
Paraproteinemias
Blood Protein Disorders
Hematologic Diseases
Hemorrhagic Disorders
Lymphoproliferative Disorders
Immunoproliferative Disorders
Immune System Diseases
Interleukin 1 Receptor Antagonist Protein
Antirheumatic Agents