Study to Assess the Safety and Tolerability of a Single Administration of FOV2302 (Ecallantide) in Patients With Macular Edema Associated With Central Retinal Vein Occlusion

Phase 1

Terminated

• Conditions: Macular Edema; Central Retinal Vein Occlusion

• Registration Number: NCT00969293
• Lead Sponsor: Fovea Pharmaceuticals SA

Brief Summary

The purpose of the study is to evaluate the safety and tolerability of a single administration of FOV2302 (ecallantide) in patients with macular edema associated with central retinal vein occlusion.

Detailed Description

Occlusive retinal vascular disease is not uncommon. Central retinal vein occlusion (CRVO) is the second most common vision-impairing vascular disorder of the retina following diabetic retinopathy. Severe visual loss from CRVO is caused by a combination of retinal edema and neovascular proliferation and ischemia. Vascular endothelial factors as they stimulate angiogenesis and increase vascular permeability, are majors pathogenic factors in CRVO. Counteracting these neovascular effects provide significant therapeutic benefit to subjects suffering from this disorder. Macular edema in this condition results from a conjunction of several, as yet, partially unknown factors.

Macular edema may occur in diseases causing cumulative injury over many years, such as diabetic retinopathy, or as a result of more acute events, such as branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO).

Study Timeline

• Study First Submitted: 2009-08-31
• Study First Submitted QC: 2009-08-31
• Study Start: 2009-09
• Study First Posted: 2009-09-01
• Primary Completion: 2011-07
• Status Verified: 2012-01
• Last Update Submitted: 2012-01-09
• Last Update Posted: 2012-01-10
• Study Completion: 2012-03

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 11

Inclusion Criteria

• Recent onset (< 6 months), non-ischemic CRVO (defined as association of documented retinal hemorrhage in all 4 quadrants of the retina with dilated veins) in patients who have not received treatment for their condition (e.g., no periocular depot or intraocular treatment [including corticosteroid and anti-VEGF], systemic corticosteroids or laser nor hemodilution).
• Retinal thickness measured by Stratus OCT > 250µm in the central subfield of study eye at baseline.
• BCVA score (measured by the ETDRS chart between 5 letters (20/800 Snellen equivalent) and 65 letters (20/50) in the study eye at baseline.
• Media clarity, pupillary dilation and participant cooperation sufficient for adequate fundus photographs.
• Females of childbearing potential using adequate birth control at Day 0 until study completion.
• Patient able (in the opinion of the investigator) and willing to return for all scheduled visits and assessments.
• Ability to read, understand and willingness to provide informed consent.

Exclusion Criteria

• Rubeosis iridis or neovascular glaucoma at baseline.
• Preretinal neovascularisation at baseline.
• Ischemic CRVO, defined by more than 10 disc area of non-perfusion on fluorescein angiography at baseline.
• Any grade of diabetic retinopathy.
• Other eye condition that could contribute to macular edema or cause retinal vascular changes (including vitreomacular traction, uveitis and inflammatory disease, etc).
• Patients who have received treatment for their condition (e.g., no periocular depot or intraocular treatment [including corticosteroid and anti-VEGF], systemic corticosteroids or laser nor hemodilution).
• Ocular surgery (including cataract extraction, scleral buckle, etc.) and/or YAG capsulotomy within 3 months preceding treatment date or anticipated within the 3 months following treatment administration.
• Poorly controlled ocular hypertension and/or glaucoma (IOP greater than 25 mmHg despite maximal therapy).
• History of pars plana vitrectomy.
• Aphakia or anterior chamber intraocular lens.
• Presence of visible sclera thinning or ectasia.
• Presence of substantial cataract or other media opacity that, in the opinion of the investigator, is likely to interfere with visualization of the fundus or completion of study measurements.
• Any active ocular or peri-ocular infection (including conjunctivitis, chalazion or significant blepharitis).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Safety and tolerability parameters to determine MTD: 1. Systemic parameters: adverse events (AEs), coagulation parameters (APTT, ACT) 2. Ophthalmologic parameters: BCVA, OCT, ocular inflammation, IOP	3 months post-dose

Secondary Outcome Measures

Name	Time	Method
Assess the pharmacodynamics up to five dose levels of a single administration of FOV2302 (ecallantide) by longitudinal measurements of the percent change of the macula thickness versus baseline as measured by OCT	3 months post-dose

Trial Locations

Locations (8)

Clinique Monticelli; 🇫🇷 Marseille, France

Centre Hospitalier National d'Ophthalmologies des XV-XX; 🇫🇷 Paris, France

Hopital Lariboisiere; 🇫🇷 Paris, France

CHU d'Amiens, Centre Saint-Victor; 🇫🇷 Amiens, France

CHU de Dijon, Hôpital Général; 🇫🇷 Dijon, France

CHU de Nantes; 🇫🇷 Nantes, France

Centre Intercommunal de Creteil; 🇫🇷 Creteil, France

Fondation Rothschild; 🇫🇷 Paris, France