drugset / Trial / NCT07616453

Efficacy and Safety of Culmerciclib Plus Aromatase Inhibitors in a Response-Adapted Neoadjuvant Strategy for Highly Proliferative ER-Positive/HER2-Negative Breast Cancer

NCT07616453

NaSequentialOpen-labelTreatment

Summary

This prospective, response-adapted phase II study evaluates the efficacy and safety of neoadjuvant culmerciclib in combination with aromatase inhibitors in patients with highly proliferative ER-positive/HER2-negative breast cancer. All patients initially receive induction treatment with culmerciclib plus endocrine therapy, followed by on-treatment assessment of biological and clinical response. Patients demonstrating an adequate response continue the same regimen, whereas those with a suboptimal response are transitioned to alternative treatment strategies prior to surgery. This adaptive approach aims to optimize treatment selection, improve therapeutic efficacy, and avoid unnecessary exposure to ineffective therapy.

Timeline

Start
2026-05-06
Primary completion
2028-05-05
Completion
2033-05-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Culmerciclib Unknown
Background Anastrozole Other / unclassified
Background Letrozole Other / unclassified