RecruitingNCT06767462

An Ophthalmic Safety Study in Patients With Breast Cancer

A Multicentre Study Assessing Ophthalmic Safety in Patients With Breast Cancer


Sponsor

AstraZeneca

Enrollment

160 participants

Start Date

Mar 4, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 YearsMax Age: 130 Years

Inclusion Criteria4

  • Signed informed consent in the qualifying study.
  • Signed informed consent in the ophthalmic study prior to any ophthalmic study specific assessments and procedures.
  • Completed the baseline ophthalmic examination for this study before the first dose in the qualifying study.
  • Meets all the eligibility criteria in the qualifying study

Exclusion Criteria3

  • Patients not randomized and not receiving study assigned treatment in a qualifying study.
  • Patients with contraindications to any ophthalmic procedure required by the study or sensitivity/allergy to pupil dilating agents.
  • Judgement by the investigator that the patient should not participate in the ophthalmic study if the patient is unlikely to comply with study procedures, restrictions, and requirements

Locations(75)

Research Site

Badalona, Spain

Research Site

Barcelona, Spain

Research Site

Barcelona, Spain

Research Site

La Jolla, California, United States

Research Site

Palo Alto, California, United States

Research Site

San Diego, California, United States

Research Site

Iowa City, Iowa, United States

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New York, New York, United States

Research Site

Winston-Salem, North Carolina, United States

Research Site

Cleveland, Ohio, United States

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Clairton, Pennsylvania, United States

Research Site

Pittsburgh, Pennsylvania, United States

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Sioux Falls, South Dakota, United States

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Bartlett, Tennessee, United States

Research Site

Houston, Texas, United States

Research Site

Buenos Aires, Argentina

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Buenos Aires, Argentina

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CABA, Argentina

Research Site

Córdoba, Argentina

Research Site

San Miguel de Tucumán, Argentina

Research Site

San Miguel de Tucumán, Argentina

Research Site

Edegem, Belgium

Research Site

Leuven, Belgium

Research Site

Liège, Belgium

Research Site

Alfenas, Brazil

Research Site

Belo Horizonte, Brazil

Research Site

Curitiba, Brazil

Research Site

Lajeado, Brazil

Research Site

Porto Alegre, Brazil

Research Site

Porto Alegre, Brazil

Research Site

Pouso Alegre, Brazil

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Rio de Janeiro, Brazil

Research Site

São Paulo, Brazil

Research Site

Sorocaba, Brazil

Research Site

Três Lagoas, Brazil

Research Site

Vitória, Brazil

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Montreal, Quebec, Canada

Research Site

Montreal, Quebec, Canada

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Santiago, Chile

Research Site

Santiago, Chile

Research Site

Santiago, Chile

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Bordeaux Cédex, France

Research Site

Caen, France

Research Site

Nantes, France

Research Site

Poitiers, France

Research Site

Suresnes, France

Research Site

Ashdod, Israel

Research Site

Nahariya, Israel

Research Site

Milan, Italy

Research Site

Aguascalientes, Mexico

Research Site

Mexico City, Mexico

Research Site

San Pedro Garza García, Mexico

Research Site

Veracruz, Mexico

Research Site

Lodz, Poland

Research Site

Nowa Sól, Poland

Research Site

Amadora, Portugal

Research Site

Braga, Portugal

Research Site

Lisbon, Portugal

Research Site

Busan, South Korea

Research Site

Daegu, South Korea

Research Site

Seoul, South Korea

Research Site

Barcelona, Spain

Research Site

Girona, Spain

Research Site

L'Hospitalet de Llobregat, Spain

Research Site

Leganés, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Madrid, Spain

Research Site

Majadahonda, Spain

Research Site

Salamanca, Spain

Research Site

Sant Joan Despí, Spain

View Full Details on ClinicalTrials.gov

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NCT06767462