Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06767462

An Ophthalmic Safety Study in Patients With Breast Cancer

A Multicentre Study Assessing Ophthalmic Safety in Patients With Breast Cancer

Status
Recruiting
Phase
Study type
Observational
Enrollment
160 (estimated)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 130 Years
Healthy volunteers
Not accepted

Summary

To assess ophthalmic health in parallel cohorts of patients with breast cancer

Detailed description

This is a multicentre study assessing the ophthalmic safety in patients who are participating in a qualifying study. The study will include two cohorts of at least 60 individuals each. To be able to account for events associated with aging, worsening of pre-existing conditions, etc., ophthalmic study assessments will be performed in parallel in two cohorts at the same timepoints. The duration of the study assessment period will be approximately 12 months. Longer duration of the study would result in additional patient burden.

Conditions

Timeline

Start date
2025-03-04
Primary completion
2027-07-06
Completion
2027-07-06
First posted
2025-01-10
Last updated
2025-07-23

Locations

75 sites across 14 countries: United States, Argentina, Belgium, Brazil, Canada, Chile, France, Israel, Italy, Mexico, Poland, Portugal, South Korea, Spain

Source: ClinicalTrials.gov record NCT06767462. Inclusion in this directory is not an endorsement.