152
Participants
Start Date
September 2, 2021
Primary Completion Date
May 25, 2027
Study Completion Date
May 25, 2027
ARV-766 Part A&B
"Part A: Daily oral dosages are determined by cohort review committee after initial starting dose cohort and each subsequent cohort completes 28 days of treatment.~Part B: Oral tablet(s) once daily in 28 day cycles."
ARV-766 + Abiraterone Part C&D
"Part C: Daily oral combination dosages are determined by cohort review committee after initial starting dose cohort and each subsequent cohort completes 28 days of treatment.~Part D: Combination administered once daily in 28 day cycles.~Parts C\&D: Participants will also receive concomitant corticosteroid and ADT therapy of investigator choice/patient preference"
Clinical Trial Site, New York
Clinical Trial Site, Buffalo
Clinical Trial Site, Pittsburgh
Clinical Trial Site, Philadelphia
Clinical Trial Site, Washington D.C.
Clinical Trial Site, Baltimore
Clinical Trial Site, Fairfax
Clinical Trial Site, Charlottesville
Clinical Trial Site, Myrtle Beach
Clinical Trial Site, Lake Mary
Clinical Trial Site, Nashville
Clinical Trial Site, Detroit
Clinical Trial Site, Madison
Clinical Trial Site, Chicago
Clinical Trial Site, New Orleans
Clinical Trial Site, San Antonio
Clinical Trial Site, Santa Monica
Clinical Trial Site, Duarte
Clinical Trial Site, La Jolla
Clinical Trial Site, Orange
Clinical Trial Site, Fresno
Clinical Trial Site, New Haven
Clinical Trial Site, Boston
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY