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Trial Summary

The primary objective of this study is to compare the progression-free survival (PFS) between sacituzumab govitecan-hziy (SG) versus treatment of physician’s choice (TPC) in participants with previously untreated, locally advanced, inoperable or metastatic triple-negative breast cancer whose tumors do not express programmed cell death ligand 1 (PD-L1) or in participants previously treated with anti-programmed cell death (ligand or protein) 1 (Anti-PD-(L)1) Agents in the early setting whose tumors do express PD-L1.

Acronym:

ASCENT 03

ACTRN/NCT /ethics:

NCT05382299

Scientific title:

Study of Sacituzumab Govitecan-hziy Versus Treatment of Physician’s Choice in Patients With Previously Untreated Metastatic Triple-Negative Breast Cancer

Sponsor / Cooperative group:

Gilead Sciences

Trial & Patient Characteristics

Cancer TypeAll cancers
Trial TypeTreatment
PhasePhase III
Age Range18 years and older
SexAll
Tumour Stream -
Cancer Stage-
Anticipated Start Date2022-07-20
Anticipated End Date2027-05-01

Participating Hospitals

HospitalCancer Research SA
Clinical Trial CoordinatorKelly Mead/Kate Penta
EmailMeggan.ORiley@socru.org.au
Phone08 8359 2565
Principal InvestigatorMeena Okera
Recruitment StatusRecruiting