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 GSK Clinical Study Register is no longer maintained for this study.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
Observational study model:
Not applicable
Primary completion date:
2012-12-04
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

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Additional information
Results for study 112855 can be found on the GSK Clinical Study Register.
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