To determine if Itacitinib in combination with corticosteroids is safe and tolerable in patients with Grade IIB-IVD acute graft-versus-host disease (GVHD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
31
All subjects will receive prednisone 2.5 mg/kg per day PO (or methylprednisolone 2 mg/kg IV daily) on Days 1 through 5. Subjects will be tapered as tolerated beginning on Day 6 to no less than 0.25 mg/kg per day PO (or methylprednisolone 0.2 mg/kg per day) by Day 28. After Day 28, corticosteroids should be tapered according to institutional guidelines to attain ≤ prednisone 0.2 mg/kg per day (or ≤ methylprednisolone 0.16 mg/kg per day) by Day 56.
Unnamed facility
Duarte, California, United States
Unnamed facility
La Jolla, California, United States
Assess safety and tolerability of study treatment as measured by the frequency and severity of adverse events and serious adverse events
Time frame: First dose of study drug to 30 days after the last dose of study drug
Overall Response Rate (ORR)
Time frame: Days 14, 28, 56 and 100
Maximum Observed Plasma Concentration (Cmax) of the two treatment groups Itacitinib
Time frame: Day 1 and Day 7
Time to Reach the Maximum Plasma Concentration (Tmax) of the two treatment groups Itacitinib
Time frame: Day 1 and Day 7
Area Under the Plasma Concentration-time Curve (AUC) of the two treatment groups Itacitinib
Time frame: Day 1 and Day 7
Minimum observed plasma concentration (Cmin) of the two treatment groups Itacitinib
Time frame: Day 1 and Day 7
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Unnamed facility
Los Angeles, California, United States
Unnamed facility
Denver, Colorado, United States
Unnamed facility
Coral Gables, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Kansas City, Kansas, United States
Unnamed facility
Westwood, Kansas, United States
Unnamed facility
New Orleans, Louisiana, United States
...and 13 more locations