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OpenTrials
Completed

NCT Number: NCT02291887

Genetic Analysis of Patients Responsive to Ranibizumab But Resistant to Aflibercept

A cohort of patients responsive to treatment with ranibizumab but resistant to

aflibercept were identified in a previously conducted retrospective study. Identified

patients will have their blood drawn for genome wide sequencing. The sequencing

data will be compiled and analyzed in an attempt to identify a common genetic basis

for patients susceptible to ranibizumab but resistant to aflibercept.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Associated Retinal Consultants

Royal Oak, Michigan, 48073, United States

About this study

A cohort of patients responsive to treatment with ranibizumab but resistant to

aflibercept were identified in a previously conducted retrospective study. Identified

patients will have their blood drawn for genome wide sequencing. The sequencing

data will be compiled and analyzed in an attempt to identify a common genetic basis

for patients susceptible to ranibizumab but resistant to aflibercept.

Blood samples will be drawn for genetic analysis for all patients enrolled in the study.

The sample (1 tube- 6mL of blood) will be collected using - 8.5mL PAXgene Blood DNA

Tubes (http://www.qiagen.com/products/catalog/sample-technologies/dna-sample-

technologies/genomic-dna/paxgene-blood-dna-tubes).

Samples will be stored at -80 until time for analysis. Note that some blood draws will be performed at

satellite clinics and transported to main facility for storage in -80 freezer. It is the understanding of

ARC PI and staff that the PAXgene Blood DNA Tubes keep samples stable at room temp for 1-2

days.

However, staff will transport samples in timely fashion (room temp, on ice, dry ice,

etc), to -80 freezer for storage until all samples are collected. Once all samples are

collected, they will be shipped to Genentech for analysis. DNA extraction, the generation of genetic

data, and subsequent analysis will be performed at Genentech or via third party. DNA will be assayed

for polymorphisms through genome wide SNP chip or whole genome sequencing. The subject's

genotype or haplotype will be correlated with their visual response and OCT response.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects will be eligible if the following criteria are met:
  • Demonstrate worsening of exudation when switched from ranibizumab to aflibercept
  • Ability to provide written informed consent and comply with study assessments for the full duration of the study

Exclusion criteria

  • Any other condition that the investigator believes would pose a significant hazard to the subject

Treatment and study plan

ranibizumab

Drug

Intravitreal injection of Ranibizumab

Other names: Lucentis

aflibercept

Drug

Intravitreal injection of Aflibercept

Other names: Eylea

Primary outcomes

  1. Genetic characteristics of patients responsive to Ranibizumab but Resistant to Aflibercept

    Time frame: 1 day

    To determine a genetic basis for patients responsive to ranibizumab but resistant to aflibercept.

Sponsors and collaborators

Lead sponsor

Associated Retinal Consultants, Michigan

Other

Collaborators

  • Genentech, Inc.

Registry information

Official study title

Genetic Analysis of Patients With Neovascular Age-Related Macular Degeneration Responsive to Ranibizumab But Resistant to Aflibercept

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Nov 17, 2014
Registry last updated
Nov 17, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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