Macugen for Histoplasmosis

NCT00272766 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2006-10-27

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and effect on visual acuity of Macugen (pegaptanib sodium) in patients with subfoveal choroidal neovascularization (CNV) secondary to the ocular histoplasmosis syndrome (OHS).

Conditions

  • Ocular Histoplasmosis
  • Choroidal Neovascularization

Interventions

DRUG

pegaptanib sodium

Sponsors & Collaborators

  • Pfizer

    collaborator INDUSTRY
  • Barnes Retina Institute

    lead OTHER

Principal Investigators

  • Gaurav K Shah, MD · Barnes Retina Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-02-28
Completion
2007-05-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00272766 on ClinicalTrials.gov