The purpose of this study is to determine the safety, pharmacokinetics, and pharmacodynamics of NKTT120 in adult patients with stable sickle cell disease.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
21
Children's Hospital & Research Center at Oakland
Oakland, California, United States
Johns Hopkins School of Medicine
Baltimore, Maryland, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Washington University School of Medicine
St Louis, Missouri, United States
Safety as assessed by (1) adverse events (2) laboratory values (3) vital signs and (4) physical exam.
Time frame: 180 days
Pharmacokinetics assessed by plasma drug concentration levels
Time frame: 0; 15, 30, 60 minutes; 3,6, hours; 1,2,3,7,14,30,60,90 days
Pharmacodynamics as measured by assessments of peripheral blood lymphocyte subsets
Time frame: 0, 0.25, 1, 2, 7, 14, 30, 60, 90, 120 days
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UNC Sickle Cell Program
Chapel Hill, North Carolina, United States
Blood Center of Wisconsin
Milwaukee, Wisconsin, United States