69
Participants
Start Date
December 22, 2014
Primary Completion Date
August 20, 2021
Study Completion Date
September 6, 2027
acalabrutinib
Participants will receive oral acalabrutinib in Cohorts 1, 2, 3, and 4. The details are mentioned in the cohort description.
Obinutuzumab
Participants will receive intravenous obinutuzumab in Cohorts 1, 2, and 4. The details are mentioned in the cohort description.
Venetoclax
Participants will receive oral venetoclax in Cohorts 3 and 4. The details are mentioned in the cohort description.
Rituximab
Participants will receive intravenous rituximab in Cohort 3. The details are mentioned in the cohort description.
Research Site, Columbus
Lead Sponsor
Acerta Pharma BV
INDUSTRY