48
Participants
Start Date
January 12, 2015
Primary Completion Date
June 26, 2020
Study Completion Date
April 1, 2026
Acalabrutinib (Arm A)
"* A1a) acalabrutinib, dose A daily: biopsy (T) schedule W;~* A1b) acalabrutinib, dose A daily: biopsy (T) schedule V.~* A2a) acalabrutinib, dose B q 12 hours: biopsy (T) schedule Y;~* A2b) acalabrutinib, dose B q 12 hours; biopsy (T) schedule Z"
Acalabrutinib (Arm B)
"B1c) acalabrutinib, dose A daily: biopsy (U) schedule W;~• B2c) acalabrutinib, dose B q12 hours: biopsy (U)) schedule Y."
Research Site, Bethesda
Lead Sponsor
National Institutes of Health (NIH)
NIH
Acerta Pharma BV
INDUSTRY