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

Primary Purpose

Leukaemia, Lymphocytic, Chronic

Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
Ofatumumab
Sponsored by
GlaxoSmithKline
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Leukaemia, Lymphocytic, Chronic focused on measuring Chronic lymphocytic leukemia, Cardiac Repolarization (QTc)

Eligibility Criteria

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

Inclusion Criteria:

  • Confirmed diagnosis of Chronic Lymphocytic Leukemia (CLL).
  • Active CLL disease and indication for treatment.
  • Previous treatment with fludarabine-containing treatment that did not achieve at least a partial response or, disease progression occurred in responders within six months of the last dose of a fludarabine-containing treatment regimen.
  • Fully active at a minimum, or fully capable of self-care and up and about more than 50% of waking hours.
  • Age 18 years or older.
  • Signed written informed consent.
  • Acceptable levels of laboratory chemistry tests of potassium and magnesium.
  • Males and female subjects must agree to use contraception (if fertile) from the time of the first dose of study medication until one year following last dose of ofatumumab.

Exclusion Criteria:

  • Any abnormal electrocardiogram (ECG) or cardiac conduction findings .
  • Certain heart problems, chronic infections, or serious significant diseases.
  • Known transformation of CLL.
  • CLL central nervous sytem involvement.
  • Abnormal/inadequate blood values, liver, or kidney function.
  • Past or current malignancy besides CLL, unless you have been free of malignancy for at least two years, have a history of completely resected non-melanoma skin cancer, or have been successfully treated.
  • Lactating women or women with a positive pregnancy test.
  • Use of medications known to prolong the heart rhythm.

Sites / Locations

  • GSK Investigational Site
  • GSK Investigational Site
  • GSK Investigational Site
  • GSK Investigational Site

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

Six months treatmet with ofatumumab will be given to subjects with chronic lymphocytic leukemia.

Outcomes

Primary Outcome Measures

Cardiac Repolarization (Fredericia's QTc)
ECGs are collected in triplicate during the study to assess QTc effect.

Secondary Outcome Measures

Plasma concentrations of ofatumumab and electrocardiogram (ECG) parameters
The pharmacokinetic results will be correlated to ECG findings to determine if drug concentrations relate to any ECG effects.
Vital signs, weight, adverse events
Safety and tolerability of ofatumumab therapy will be determined by analysing changes in vital signs, weight, or development of adverse events.
Flow cytometry
Efficacy of ofatumumab therapy will be measured by the number of CD20 positive cells in the blood
Cytokine, chemokine, human anti-human antibodies
Effect of ofatumumab on circulating biomarkers in refractory Chronic Lymphocytic Leukemia (CLL) subjects will be determined by measuring changes in the cytokine, chemokine, human anti-human antibody levels.

Full Information

First Posted
April 22, 2010
Last Updated
November 8, 2017
Sponsor
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT01110031
Brief Title
Ofatumumab Cardiac Repolarization (QTc) Study in Fludarabine-Refractory Chronic Lymphocytic Leukemia Subjects
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
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
May 13, 2010 (Actual)
Primary Completion Date
April 12, 2012 (Actual)
Study Completion Date
June 26, 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GlaxoSmithKline

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
The purpose of this trial is to assess the impact of ofatumumab on electrocardiographic parameters with particular focus on cardiac repolarization (QTc interval duration) in subjects with refractory Chronic Lymphocytic Leukemia (CLL).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leukaemia, Lymphocytic, Chronic
Keywords
Chronic lymphocytic leukemia, Cardiac Repolarization (QTc)

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
Six months treatmet with ofatumumab will be given to subjects with chronic lymphocytic leukemia.
Intervention Type
Biological
Intervention Name(s)
Ofatumumab
Other Intervention Name(s)
Arzerra
Intervention Description
Anti-CD20 monoclonal antibody
Primary Outcome Measure Information:
Title
Cardiac Repolarization (Fredericia's QTc)
Description
ECGs are collected in triplicate during the study to assess QTc effect.
Time Frame
25-week ofatumumab treatment period
Secondary Outcome Measure Information:
Title
Plasma concentrations of ofatumumab and electrocardiogram (ECG) parameters
Description
The pharmacokinetic results will be correlated to ECG findings to determine if drug concentrations relate to any ECG effects.
Time Frame
25-week ofatumumab treatment period
Title
Vital signs, weight, adverse events
Description
Safety and tolerability of ofatumumab therapy will be determined by analysing changes in vital signs, weight, or development of adverse events.
Time Frame
25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion
Title
Flow cytometry
Description
Efficacy of ofatumumab therapy will be measured by the number of CD20 positive cells in the blood
Time Frame
25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion
Title
Cytokine, chemokine, human anti-human antibodies
Description
Effect of ofatumumab on circulating biomarkers in refractory Chronic Lymphocytic Leukemia (CLL) subjects will be determined by measuring changes in the cytokine, chemokine, human anti-human antibody levels.
Time Frame
25-week ofatumumab treatment period plus 6-month follow-up after final ofatumumab infusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed diagnosis of Chronic Lymphocytic Leukemia (CLL). Active CLL disease and indication for treatment. Previous treatment with fludarabine-containing treatment that did not achieve at least a partial response or, disease progression occurred in responders within six months of the last dose of a fludarabine-containing treatment regimen. Fully active at a minimum, or fully capable of self-care and up and about more than 50% of waking hours. Age 18 years or older. Signed written informed consent. Acceptable levels of laboratory chemistry tests of potassium and magnesium. Males and female subjects must agree to use contraception (if fertile) from the time of the first dose of study medication until one year following last dose of ofatumumab. Exclusion Criteria: Any abnormal electrocardiogram (ECG) or cardiac conduction findings . Certain heart problems, chronic infections, or serious significant diseases. Known transformation of CLL. CLL central nervous sytem involvement. Abnormal/inadequate blood values, liver, or kidney function. Past or current malignancy besides CLL, unless you have been free of malignancy for at least two years, have a history of completely resected non-melanoma skin cancer, or have been successfully treated. Lactating women or women with a positive pregnancy test. Use of medications known to prolong the heart rhythm.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GSK Clinical Trials
Organizational Affiliation
GlaxoSmithKline
Official's Role
Study Director
Facility Information:
Facility Name
GSK Investigational Site
City
La Jolla
State/Province
California
ZIP/Postal Code
92093
Country
United States
Facility Name
GSK Investigational Site
City
Randwick
State/Province
New South Wales
ZIP/Postal Code
2031
Country
Australia
Facility Name
GSK Investigational Site
City
Auckland
ZIP/Postal Code
1150
Country
New Zealand
Facility Name
GSK Investigational Site
City
Christchurch
ZIP/Postal Code
8011
Country
New Zealand

12. IPD Sharing Statement

Citations:
PubMed Identifier
25103870
Citation
Jewell RC, Laubscher K, Lewis E, Fang L, Gafoor Z, Carey J, McKeown A, West S, Wright O, Sedoti D, Dixon I, Hottenstein CS, Chan G. Assessment of the effect of ofatumumab on cardiac repolarization. J Clin Pharmacol. 2015 Jan;55(1):114-21. doi: 10.1002/jcph.376. Epub 2014 Aug 21.
Results Reference
derived

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

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