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Survival Outcomes, Adverse Events and Predictive Biomarkers for CDK4/6 Inhibitors in Patients With Hormone Receptor-positive Advanced Breast Cancer, an Ambispective Single-center Cohort Study
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT05795335
Status
RECRUITING
Phase
Observational Study
Sponsor
RenJi Hospital
Executive brief
Investment-Ready Snapshot
This ambispective cohort study sponsored by RenJi Hospital aims to evaluate the survival outcomes, adverse events, and predictive biomarkers associated with CDK4/6 inhibitors in patients with hormone receptor-positive advanced breast cancer. The study is currently recruiting participants and is expected to provide valuable insights into the efficacy and safety of CDK4/6 inhibitors, which are a growing class of therapies in oncology. The findings could enhance the competitive positioning of CDK4/6 inhibitors in the market, particularly as the demand for targeted therapies in breast cancer continues to rise. Additionally, the study may inform future clinical development strategies and potential partnerships for further research in this therapeutic area.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05795335
Indication
Breast Cancer
Modality
small molecule
Target
CDK4/6 (Cyclin-Dependent Kinase 4 and 6)
Intervention
CDK4/6 inhibitor
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.