40
Participants
Start Date
February 17, 2021
Primary Completion Date
September 8, 2023
Study Completion Date
February 27, 2025
AZD4573
AZD4573 will be administered as an absolute (flat) dose, 2-hour (± 15 minutes) IV infusion once weekly (as monotherapy for Module 2 only) and in combination with orally administered acalabrutinib twice daily continuously. For both Part A and Part B of this study, Cycle 1 consists of 5 weeks, with a dose ramp-up. Subsequent cycles are 21 days (3 weeks) with once weekly dosing of AZD4573 in combination with acalabrutinib twice daily continuously (in Module 1 and Module 2, period 2).
Acalabrutinib
Oral Acalabrutinib capsule will be administered twice daily continuously from Day 1 of Cycle 1 Week 1 in combination with AZD4573.
Research Site, Clayton
Research Site, Nedlands
Research Site, Lille
Research Site, Houston
Research Site, Salt Lake City
Research Site, Duarte
Research Site, La Jolla
Research Site, Québec
Research Site, Dublin
Research Site, Galway
Research Site, Krakow
Research Site, Seoul
Research Site, Seoul
Research Site, Seoul
Research Site, Barcelona
Research Site, Palma de Mallorca
Research Site, Plymouth
Lead Sponsor
Collaborators (1)
Parexel
INDUSTRY
AstraZeneca
INDUSTRY