Actively Recruiting

Age: 18Years - 90Years
All Genders
NCT06905301

Implementation Study to Describe and Compare Retention Rate and Adherence to Adjuvant Therapy With Ribociclib With and Without Usage of Mobile Application in Patients With HR+ HER2-negative Stage II and III Breast Cancer in Real-world Practice

Led by Novartis Pharmaceuticals · Updated on 2026-05-05

240

Participants Needed

7

Research Sites

205 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is designed to evaluate the effect of using the application on the adherence of patients with luminal HER2- breast cancer (BC) stage II-III to adjuvant therapy with ribociclib in combination with an aromatase inhibitor (AI). The purpose of the app is to increase adherence to treatment by informing patients about the risks of relapse and adverse event prevention and treatment.

CONDITIONS

Official Title

Implementation Study to Describe and Compare Retention Rate and Adherence to Adjuvant Therapy With Ribociclib With and Without Usage of Mobile Application in Patients With HR+ HER2-negative Stage II and III Breast Cancer in Real-world Practice

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Female and male patients with histologically verified and radically treated stage II-III hormone receptor positive HER2-negative breast cancer
  • Age 18 years or older at start of ribociclib therapy
  • Prescribed ribociclib plus aromatase inhibitor (± GnRH agonist for premenopausal patients) within 28 days before signing consent
  • Allowed to have started aromatase inhibitor therapy (± GnRH agonist) no earlier than 12 months before ribociclib start
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Currently participating in any interventional clinical study when signing consent
  • Receiving active treatment for malignant neoplasms other than breast cancer at enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

Novartis Investigative Site

Pskov, Russia, Russia, 180000

Actively Recruiting

2

Novartis Investigative Site

Moscow, Russia, 115304

Actively Recruiting

3

Novartis Investigative Site

Saint Petersburg, Russia, 194017

Actively Recruiting

4

Novartis Investigative Site

Saint Petersburg, Russia, 194291

Actively Recruiting

5

Novartis Investigative Site

Saint Petersburg, Russia, 197758

Actively Recruiting

6

Novartis Investigative Site

Sestroretsk, Russia, 197706

Actively Recruiting

7

Novartis Investigative Site

Ufa, Russia, 450054

Actively Recruiting

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Research Team

N

Novartis Pharmaceuticals

CONTACT

N

Novartis Pharmaceuticals

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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