Last updated: 11/07/2018 05:17:30
This product has been transferred to Novartis. GSK Clinical Study Register is no longer maintained for this study. The most up to date information is available on clinicaltrials.gov.

Ofatumumab Cardiac Repolarization (QTc) Study in Fludarabine-Refractory Chronic Lymphocytic Leukemia Subjects

GSK study ID
112855
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
No longer a GSK study
No longer a GSK study
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: An Open-Label, Single-Arm, Phase I Study to Evaluate the Effect of Ofatumumab on Cardiac Repolarization (QTc Duration) in Patients with Fludarabine-Refractory B-cell Chronic Lymphocytic Leukemia
Trial description: Ofatumumab is a fully-human monoclonal antibody that exhibits high binding affinity to an antigen on the surface of B lymphocytes. Antigen engagement by ofatumumab results in maximal B-cell killing through complement-dependent cytotoxicity and antigen-dependent cellular cytotoxicity in both antigen high- and low-expressing cells. Recent research has shown that ofatumumab-dependent B-cell depletion provides clinical benefit to subjects with CD20-positive cancers such as chronic lymphocytic leukemia (CLL). The purpose of the current study is to assess the impact of ofatumumab on electrocardiographic parameters with particular focus on cardiac repolarization (QTc interval duration) in subjects with refractory CLL. Subjects enrolled in this open-label, single-arm trial will receive ofatumumab at the highest clinical dose (2000 mg) studied or planned for study. Ofatumumab will be administered as eight weekly intravenous (IV) infusions followed by four monthly infusions, beginning in Week 13, across a 25-week treatment period. Cardiovascular effects will be evaluated during treatment through routine 12-lead electrocardiographic (ECG) monitoring. The pharmacokinetic relationship between plasma concentration of ofatumumab and its effect on QTc interval duration will be examined. Specifically, ECG assessments will be collected in triplicate at baseline, at the time of maximum ofatumumab concentrations periodically on-therapy, and at the end of treatment. After completion of the final ofatumumab infusion, subjects will continue to be followed for safety and efficacy for six months relative to the last ofatumumab dose.
Primary purpose:
Other
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Non-randomized
Primary outcomes:

Cardiac Repolarization (Fredericia's QTc)

Timeframe: 25-week ofatumumab treatment period

Secondary outcomes:

Plasma concentrations of ofatumumab and electrocardiogram (ECG) parameters

Timeframe: 25-week ofatumumab treatment period

Vital signs, weight, adverse events

Timeframe: 25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion

Flow cytometry

Timeframe: 25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion

Cytokine, chemokine, human anti-human antibodies

Timeframe: 25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion

Interventions:
  • Biological/vaccine: Ofatumumab
  • Enrollment:
    12
    Primary completion date:
    2012-12-04
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    William Nigel Patton, Robert Lindeman, Andrew C. Butler, Thomas J. Kipps, Roxanne C. Jewell, Kevin H. Laubscher, Eric Lewis, Donna Sedoti, Philip Witman, Geoffrey Chan.An Open-Label, Single-Arm, Phase 1 Study to Assess Biomarker Effects, Efficacy, and Safety of Ofatumumab in Patients With Refractory Chronic Lymphocytic Leukemia .Leuk Lymphoma.2015;56(10):2819-2825.
    Medical condition
    Leukaemia, Lymphocytic, Chronic
    Product
    ofatumumab
    Collaborators
    Not applicable
    Study date(s)
    May 2010 to June 2012
    Type
    Interventional
    Phase
    1

    Participation criteria

    Sex
    Female & Male
    Age
    18+ years
    Accepts healthy volunteers
    No
    • Confirmed diagnosis of Chronic Lymphocytic Leukemia (CLL).
    • Active CLL disease and indication for treatment.
    • Any abnormal electrocardiogram (ECG) or cardiac conduction findings .
    • Certain heart problems, chronic infections, or serious significant diseases.

    Trial location(s)

    Location
    Status
    Contact us
    Contact us
    Location
    GSK Investigational Site
    Christchurch, New Zealand, 8011
    Status
    Study Complete
    Location
    GSK Investigational Site
    Auckland, New Zealand, 1150
    Status
    Study Complete
    Location
    GSK Investigational Site
    La Jolla, California, United States, 92093
    Status
    Study Complete
    Location
    GSK Investigational Site
    Randwick, New South Wales, Australia, 2031
    Status
    Study Complete

    Study documents

    Clinical study report
    Available language(s): English
    Scientific result summary
    Available language(s): English
    Protocol
    Available language(s): English

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Refer to study documents

    Recruitment status
    No longer a GSK study
    Actual primary completion date
    2012-12-04
    Actual study completion date
    2012-26-06

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

    Participate in clinical trial
    Additional information
    Results for study 112855 can be found on the GSK Clinical Study Register.
    Click here
    Access to clinical trial data by researchers
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