Study identifier:D3615R00004
ClinicalTrials.gov identifier:NCT07008963
EudraCT identifier:N/A
CTIS identifier:N/A
A non-interventional, observational qualitative interview study of patients with HR+/HER2- metastatic breast cancer who received capivasertib + fulvestrant
Metastatic Breast Cancer
N/A
No
-
All
50
Observational
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Jun 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
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