Ofatumumab Cardiac Repolarization (QTc) Study in Fludarabine-Refractory Chronic Lymphocytic Leukemia Subjects
Trial overview
Cardiac Repolarization (Fredericia's QTc)
Timeframe: 25-week ofatumumab treatment period
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
- 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.
- 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.
•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.
•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.
Trial location(s)
Study documents
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
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.