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Macugen Injections for Age-Related Macular Degeneration
Phase 4
Waitlist Available
Research Sponsored by Eyetech Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients who have had at least 1 but not more than 3 prior treatments for AMD
Patients with subfoveal CNV secondary to AMD
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is testing if Macugen is effective and safe to use as maintenance therapy for Neovascular Age-Related Macular Degeneration for patients who have had success with other treatments.
Who is the study for?
This trial is for people with a condition called Age-Related Macular Degeneration (AMD) who have had some success with up to three previous treatments. They must have a specific type of AMD where abnormal blood vessels grow under the retina, but can't join if they have eye conditions like cataracts that could affect vision or scars in the central part of their retina.Check my eligibility
What is being tested?
The study is testing the safety and effectiveness of an eye injection called Macugen when given every six weeks as ongoing treatment for AMD. It's aimed at those who've seen improvements from earlier AMD therapies.See study design
What are the potential side effects?
While not specified here, common side effects of similar eye injections may include eye irritation or pain, blurred vision, feeling like something is in your eye, and possible bleeding inside the eye.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have had 1 to 3 treatments for age-related macular degeneration.
Select...
I have AMD-related vision loss due to abnormal blood vessels.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
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Who is running the clinical trial?
Eyetech PharmaceuticalsLead Sponsor
14 Previous Clinical Trials
2,087 Total Patients Enrolled
PfizerIndustry Sponsor
4,567 Previous Clinical Trials
10,907,303 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have scarring or tissue loss in the center of my retina.I have had 1 to 3 treatments for age-related macular degeneration.I have AMD-related vision loss due to abnormal blood vessels.I have eye conditions like cataracts that affect my vision.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 3 awards, including:- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are recruitment initiatives currently ongoing for this investigation?
"This particular clinical trial is not presently enrolling participants, as indicated by the information on clinicaltrials.gov. It was initially posted on June 1st 2006 and last revised January 12th 2007; however, there are 159 other studies currently accepting applicants."
Answered by AI
To what degree is this therapy perilous for individuals?
"After assessing the available data, Power's team has assigned this treatment a 3 out of 3 for safety due to it being in Phase 4 trials and having received approval."
Answered by AI
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