Study Evaluating Genotypes Using Lucentis

NCT00474695 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2015-02-11

No results posted yet for this study

Summary

The purpose of the study is to investigate whether the efficacy of Lucentis treatment for exudative age-related macular degeneration is associated with VEGF and HTRA1 DNA polymorphisms

Conditions

  • Age-Related Maculopathy

Interventions

DRUG

Lucentis

0.05 mg intravitreal injection

Sponsors & Collaborators

Principal Investigators

  • Paul Bernstein, MD, PhD · University of Utah

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2009-06-30
Completion
2009-12-31

Countries

  • United States

Study Locations

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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 NCT00474695 on ClinicalTrials.gov