Treatment Patterns of Neratinib in HER2+ EBC in China

NCT05491057 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2022-08-08

No results posted yet for this study

Summary

This is a multicenter, open-label, single-arm, non-interventional study to investigate the treatment patterns of Neratinib in HER2-positive early-stage breast cancer in China

Conditions

Interventions

DRUG

Neratinib

Neratinib standard dose 240 mg once daily for 1 year

Sponsors & Collaborators

  • Pierre Fabre Medicament

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-30
Primary Completion
2025-12-30
Completion
2026-06-30

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05491057 on ClinicalTrials.gov