The purpose of this study is to determine if HGS1029 is safe and well tolerated in patients with relapsed or refractory lymphoid malignancies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
11
HGS1029 will be given as a 15-minute IV infusion (in the vein) once weekly for 3 consecutive weeks, followed by 1 week off.
Mayo Clinic
Rochester, Minnesota, United States
Hackensack University Medical Center
Hackensack, New Jersey, United States
Oxford Cancer and Haematology Centre
Headington, Oxford, United Kingdom
The Institute of Cancer Research
Belmont, Sutton, Surrey, United Kingdom
Type, frequency and severity of adverse events
Time frame: 1 year
Measure pharmacokinetic profile
Time frame: 1st two months of the study
Evaluation of pharmacodynamics
Time frame: 1st two months of the study
Evaluation of possible anti-tumor activity
Time frame: Every 2 months while on study
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Cancer Research UK Centre
Southampton, United Kingdom