396
Participants
Start Date
October 11, 2018
Primary Completion Date
September 16, 2024
Study Completion Date
December 31, 2026
AZD9833
Part A: AZD9833 monotherapy dose escalation.
AZD9833
Part B: AZD9833 monotherapy expansion.
AZD9833 with palbociclib
Part C: AZD9833 in combination with palbociclib dose escalation
AZD9833 with palbociclib
Part D: AZD9833 in combination with palbociclib expansion
AZD9833 with everolimus
Part E: AZD9833 in combination with everolimus dose escalation
AZD9833 with everolimus
Part F: AZD9833 in combination with everolimus dose expansion
AZD9833 with abemaciclib
Part G: AZD9833 in combination with abemaciclib (± anastrozole) dose escalation
AZD9833 with abemaciclib
Part H: AZD9833 in combination with abemaciclib (± anastrozole) dose expansion
AZD9833 with capivasertib
Part I: AZD9833 in combination with capivasertib dose escalation
AZD9833 with capivasertib
Part J: AZD9833 in combination with capivasertib dose expansion
AZD9833 with ribociclib
Part K: AZD9833 in combination with ribociclib (± anastrozole) dose escalation
AZD9833 with ribociclib
Part L: AZD9833 in combination with ribociclib (± anastrozole) dose expansion
AZD9833 with anastrozole
Part M: AZD9833 in combination with anastrozole dose escalation
AZD9833 with anastrozole
Part N: AZD9833 in combination with anastrozole dose expansion
Research Site, Barcelona
Research Site, Philadelphia
Research Site, Madrid
Research Site, Madrid
Research Site, Sarasota
Research Site, Nashville
Research Site, Seville
Research Site, Valencia
Research Site, Aurora
Research Site, Salt Lake City
Research Site, Barcelona
Research Site, Cambridge
Research Site, Leeds
Research Site, London
Research Site, Manchester
Research Site, Sutton
Research Site, Sutton
Lead Sponsor
AstraZeneca
INDUSTRY