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| Sponsored by: |
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery |
|---|---|
| Information provided by: | The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery |
| ClinicalTrials.gov Identifier: | NCT00531336 |
Purpose
The first results of Anti-Vascular Endothelial Growth Factor (VEGF) therapy were very promising and superior to established therapies. Three different substances (all of them applied intravitreally) are available, but comparative studies have not yet been conducted. In this pilot study, the safety (number of adverse events) and efficacy (distance acuity testing retinal thickness measurement) of Avastin and Macugen applied as monotherapy will be compared to a combined treatment of Avastin followed by Macugen used for retreatment.
At least equal results of the combined therapy are expected.
| Condition | Intervention | Phase |
|---|---|---|
|
Macular Degeneration |
Drug: intravitreal injection of Bevacizumab (Avastin) Drug: Pegaptanib (Macugen) |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | Comparison of Combined Therapy of Intravitreal Injection of Avastin and Macugen Versus Mono-Therapy The MAAM Study - a Pilot Study |
| Estimated Enrollment: | 60 |
| Study Start Date: | July 2006 |
| Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
1: Experimental
Avastin first followed by retreatment of Macugen
|
Drug: intravitreal injection of Bevacizumab (Avastin)
1.25 mg Avastin intravitraeally applied once in arm 1 every 6 weeks in arm 2
Drug: Pegaptanib (Macugen)
0.3 mg intravitreally applied every 6 weeks as long as required
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2: Active Comparator
Avastin intravitreally every 6 weeks
|
Drug: intravitreal injection of Bevacizumab (Avastin)
1.25 mg Avastin intravitraeally applied once in arm 1 every 6 weeks in arm 2
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3: Active Comparator
Macugen intravitreally every 6 weeks
|
Drug: Pegaptanib (Macugen)
0.3 mg intravitreally applied every 6 weeks as long as required
|
The role of Vascular Endothelial Growth Factor (VEGF) in the pathogenesis of neovascular diseases like choroidal neovascularization (CNV) and proliferative diabetic retinopathy has been demonstrated in a series of publications. Therefore intravitreally applied VEGF antagonists have been used in the treatment of CNV in age-related macular degeneration (AMD) and diabetic cases. Three anti-VEGFs are available: Macugen® (Pegaptanib), Avastin® (Bevacizumab) and Lucentis® (Ranibizmab). Pegaptanib sodium is an aptamer designed to bind the VEGF 165 isoform with high affinity. Bevacizumab is a humanized monoclonal antibody to VEGF designed for intravenous administration and approved for the treatment of colorectal cancer. Ranibizumab is an anti-body binding site fragment that is derived from the same anti-VEGF antibody as bevacizumab. The decrease of retinal thickness measured in the OCT provides information concerning the amount of intraretinal fluid accumulation and therefore for the activity of a neovascular lesion. It has been proven that the aqueous humor levels of VEGF of eyes with CNV are significantly higher than those of eyes without ocular or systemic diseases. The retinal thickness and the VEGF concentration in the aqueous humor should give a good correlation to the anti vasogenic effect of the intravitreal treatment. In this study bevacizumab and pegaptanib as monotherapy should be compared with a combined therapy of bevacizumab applied first with pegaptanib used for retreatment. The benefit of this combined therapy should be that an initial blockage of all VEGF isoforms is necessary whereas for retreatment the blockage of the most important isoform in the pathogenesis of CNV is sufficient and the normal function of the retinal pigment epithelium and the choriocapillaris is not affected.
Eligibility| Ages Eligible for Study: | 50 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Austria | |
| Ludwig Boltzmann Institute for Retinology and Biomicroscopic Lasersurgery | |
| Vienna, Austria, A1030 | |
| Principal Investigator: | Ilse Krebs, MD | Ludwig Boltzmann Institute for Biomicroscopic Lasersurgery |
More Information
| Responsible Party: | The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery ( Susanne Binder Prof ) |
| Study ID Numbers: | EK06-001839-18 |
| Study First Received: | September 15, 2007 |
| Last Updated: | October 30, 2008 |
| ClinicalTrials.gov Identifier: | NCT00531336 |
| Health Authority: | Austria: Ethikkommission |
|
age-related Macular degeneration Macugen Avastin |
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Eye Diseases Retinal Degeneration Macular Degeneration |
Bevacizumab Retinal Diseases Retinal degeneration |
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Antineoplastic Agents Therapeutic Uses Growth Substances Physiological Effects of Drugs |
Growth Inhibitors Angiogenesis Modulating Agents Angiogenesis Inhibitors Pharmacologic Actions |
