ClinicaliQ Trial Snapshot
- An Adjuvant Endocrine-based Therapy Study of Camizestrant (AZD9833) in ER+/HER2- Early Breast Cancer (CAMBRIA-2) — Recruiting • Phase III • Oncology • NCT05952557.
- What is being tested: Camizestrant (AZD9833), a selective oestrogen receptor degrader (SERD), is being compared to standard adjuvant endocrine therapy (aromatase inhibitors or tamoxifen) in early breast cancer to determine whether it improves disease-free survival and overall survival outcomes.
- Patient eligibility overview: The trial includes patients with oestrogen receptor-positive, HER2-negative early breast cancer at intermediate-high or high risk of recurrence who have completed surgery and/or radiotherapy, with treatment decisions guided by standard clinicopathological and genomic risk assessment tools.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
This is a Phase III open-label study to assess if camizestrant improves outcomes compared to standard adjuvant endocrine therapy for patients with ER+/HER2- early breast cancer with intermediate-high or high risk for disease recurrence who completed definitive locoregional therapy (with or without chemotherapy). The planned duration of treatment in either arm within the study will be 7 years.
Eligibility Snapshot
- : * Women and Men; ≥18 years at the time of screening (or per national guidelines) * Histologically confirmed ER+/HER2- early-stage resected invasive breast cancer with absence of any evidence of metastatic disease as defined in the protocol. * Completed adequate (definitive) locoregional therapy (surgery with or without radiotherapy) for the primary breast tumour(s), with or without (neo)adjuvant chemotherapy. * Patients must be randomised within 12 months of definitive breast surgery. * Patients may have received up to 12 weeks of endocrine therapy prior to randomisation. * Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1 * Adequate organ and bone marrow function
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.