✓. ALT and/or AST ≤ 3 x ULN, and bilirubin and ALP ≤ 2 x ULN.
Exclusion criteria
✕8. Ability to understand and the willingness to sign a written informed consent document.
✕9. Agree to sign consent to the long-term follow-up protocol PA17-0843 to fulfill the institutional responsibilities to various regulatory agencies.
✕. Lymphoma in CR with no measurable sites of disease.
✕. Major surgery \<4 weeks prior to first dose of study drug.
✕. Any other severe or uncontrolled disease or condition which might increase the risk associated with study participation.
What they're measuring
1
Safety and Adverse Events (AEs)
Timeframe: Through study completion; an average of 1 year