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Extended Use of Cannabidiol for the Prevention of Graft-versus-host-disease

Primary Purpose

Graft vs Host Disease

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Cannabidiol
cyclosporine
Methotrexate
Sponsored by
Rabin Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Graft vs Host Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Acute leukemia in complete remission
  2. Myeloablative conditioning
  3. Matched or one antigen or allele mismatched sibling or unrelated donor

Exclusion Criteria:

  1. History of psychosis
  2. Bronchial asthma

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Cannabidiol arm

    Arm Description

    Patients undergoing an allogeneic hematopoietic cell transplantation will be given standard GVHD prophylaxis comprising cyclosporine and a short course of methotrexate plus CBD 150 mg BID starting 7 days before transplantation until day 100.

    Outcomes

    Primary Outcome Measures

    Incidence of grade 2-4 and grade 3-4 acute GVHD by day 100
    grade 3-4 adverse effects attributed to CBD consumption
    Incidence of overall chronic GVHD and moderate to severe chronic GVHD by 12 months
    Incidence of late onset acute GVHD

    Secondary Outcome Measures

    Non relapse mortality
    Relapse rate
    Overall survival
    Adherence to study protocol
    Percentage of doses actually taken as reported by patients
    Disease free and immunosuppression free survival by 12 months

    Full Information

    First Posted
    June 15, 2015
    Last Updated
    June 22, 2015
    Sponsor
    Rabin Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02478424
    Brief Title
    Extended Use of Cannabidiol for the Prevention of Graft-versus-host-disease
    Official Title
    Extended Use of Cannabidiol for the Prevention of Graft-versus-host Disease After Allogeneic Hematopoietic Cell Transplantation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    July 2015 (undefined)
    Primary Completion Date
    December 2016 (Anticipated)
    Study Completion Date
    June 2017 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Rabin Medical Center

    4. Oversight

    5. Study Description

    Brief Summary
    Cannabidiol (CBD), a non-psychotropic ingredient of Cannabis sativa possesses potent anti-inflammatory and immunosuppressive properties. In a recent prospective phase II study (NCT01385124) 48 consecutive adult patients undergoing allogeneic hematopoietic cell transplantation were given CBD 300 mg/day starting 7 days before transplantation until day 30, on top of standard GVHD prophylaxis consisting of cyclosporine and a short course of methotrexate. There were no grade 3-4 toxicities attributed to CBD. None of the patients developed acute GVHD while consuming CBD. With a median follow-up of 16 months, the cumulative incidence rates of grade 2-4 and grade 3-4 acute GVHD by day 100 were 12.1% and 5%, respectively. Compared to 101 historical control subjects given standard GVHD prophylaxis, the hazard ratio of developing grade 2-4 acute GVHD among subjects treated with CBD plus standard GVHD prophylaxis was 0.3 (p=0.0002). Among patients surviving more than 100 days, the cumulative incidence of moderate-to-severe chronic GVHD at 12 and 18 months were 20% and 33%, respectively. The aim of this study is to explore the safety and efficacy of extended use of CBD until day 100 in the prevention of acute and chronic GVHD.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Graft vs Host Disease

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    10 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Cannabidiol arm
    Arm Type
    Experimental
    Arm Description
    Patients undergoing an allogeneic hematopoietic cell transplantation will be given standard GVHD prophylaxis comprising cyclosporine and a short course of methotrexate plus CBD 150 mg BID starting 7 days before transplantation until day 100.
    Intervention Type
    Drug
    Intervention Name(s)
    Cannabidiol
    Other Intervention Name(s)
    CBD
    Intervention Description
    Patients will receive standard GVHD prophylaxis consisting of cyclosporine A twice daily starting on day -1 with target trough levels of 200-400 ng/mL and a short course of methotrexate (15 mg/ m2 on day 1 and 10 mg/ m2 on days days 3 and 6). Patients transplanted from unrelated donors will receive ATG Fresenius at a low dose of 5 mg/kg on days -3 to -1. Patients will be given oral CBD 150 mg BID starting 7 days before transplantation until day 100.
    Intervention Type
    Drug
    Intervention Name(s)
    cyclosporine
    Intervention Type
    Drug
    Intervention Name(s)
    Methotrexate
    Primary Outcome Measure Information:
    Title
    Incidence of grade 2-4 and grade 3-4 acute GVHD by day 100
    Time Frame
    100 days
    Title
    grade 3-4 adverse effects attributed to CBD consumption
    Time Frame
    180 days
    Title
    Incidence of overall chronic GVHD and moderate to severe chronic GVHD by 12 months
    Time Frame
    12 months
    Title
    Incidence of late onset acute GVHD
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    Non relapse mortality
    Time Frame
    12 months
    Title
    Relapse rate
    Time Frame
    12 months
    Title
    Overall survival
    Time Frame
    12 months
    Title
    Adherence to study protocol
    Description
    Percentage of doses actually taken as reported by patients
    Time Frame
    Until day 100
    Title
    Disease free and immunosuppression free survival by 12 months
    Time Frame
    12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Acute leukemia in complete remission Myeloablative conditioning Matched or one antigen or allele mismatched sibling or unrelated donor Exclusion Criteria: History of psychosis Bronchial asthma
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Moshe Yeshurun, MD
    Phone
    972-50-4065543
    Email
    moshey@clalit.org.il
    First Name & Middle Initial & Last Name or Official Title & Degree
    Liat Shargian, MD
    Phone
    972-54-2394930
    Email
    LIATSHR@clalit.org.il

    12. IPD Sharing Statement

    Learn more about this trial

    Extended Use of Cannabidiol for the Prevention of Graft-versus-host-disease

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