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Clinical Trials in Sweden / NCT04654208
Recruiting Observational

Swedish Ibrance Registries Insights (SIRI)

NCT04654208 · tracked via the Priya Life Science Sweden tracker
Sponsor
Phase
Observational
Started
2020-12-15
Last updated
2026-03-31

Condition(s) studied

Malignant Neoplasm of Breast

Investigational drug(s) / intervention(s)

palbociclib →

palbociclib: patients on palbociclib combination treatment

Study summary

The main objectives of this study are to describe patient characteristics, treatment patterns and clinical outcomes of patients receiving palbociclib in Swedish clinical practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study: 1. One or more (≥1) filled prescription of palbociclib (ATC code: L01XE33) 2. Age ≥18 years at index date Exclusion Criteria: There are no exclusion criteria

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Pfizer Sweden Sollentuna Sweden Recruiting

On this site

📄 Ibrance (palbociclib) drug profile →

More Pfizer trials in Sweden

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04654208 on ClinicalTrials.gov ↗ ← All trials in Sweden