Bevacizumab in Combination With Verteporfin Reduced and Standard Fluence in the Treatment of Hemorrhaged Lesions in Neovascular AMD

Stopped early · Phase 1

Conditions studied: Macular Degeneration

In brief

The purpose of this study is to explore the combination of PDT with verteporfin at reduced and standard fluence rates, in conjunction with bevacizumab, in the treatment of subfoveal CNV of all subtypes with a high percentage of subretinal hemorrhage (hemorrhage \>50% of total lesion area). To assess the safety of bevacizumab in combination with verteporfin PDT (reduced fluence: 300 mW/cm2) as compared to bevacizumab in combination with verteporfin PDT (standard fluence: 600 mW/cm2) in patients whose neovascular CNV lesions containing \>50% blood.

Key facts

Study ID

NCT00403442

Run by

Vitreous -Retina- Macula Consultants of New York

People needed

10

Starts

2006-09-01

Last updated by the study team

2008-07-30

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients are men or women of age 50 or older.
• Patients diagnosed with subfoveal CNV due to AMD with lesion size ≤6 DA.
• Patients have not received previous treatment for subfoveal CNV, in the study eye.
• Patients with visual acuities at baseline between 20/40 and 20/320, as evaluated on ETDRS scale.
• Fluorescein Angiography showing any type of subfoveal CNV at baseline with >50% blood component of total lesion area.

You may not qualify if…

• Patients with a known hypersensitivity/allergy to verteporfin, porfimer sodium, or other porphyrins, porphyria or other porphyrin sensitivity, or hypersensitivity to sunlight or bright artificial light.
• Patients with history of glaucoma requiring treatment, or are currently on antihypertensive treatment for elevated intraocular pressure.
• Women of childbearing potential must not be pregnant of lactating, must have a negative pregnancy test at screening and must be practicing an adequate method of birth control.
• Patients who have had treatment for CNV in the study eye with photodynamic therapy (PDT), transpupillary thermotherapy (TTT), or other local treatment (e.g. submacular surgery, intravitreal triamcinolone, intra-ocular antiangiogenic agents). Previous laser photocoagulation therapy is acceptable, provided it was not subfoveal.
• Subject's currently who have been involved in any experimental procedure within the last 12 weeks.

Where it is running

• Vitreous Retina Macula Consultants of New York, P.C. — New York, New York, United States

Full record on ClinicalTrials.gov

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