RHEO-AMD: Safety and Effectiveness Investigation for Dry, Non-Exudative Age Related Macular Degeneration (AMD) Using Rheopheresis

Sponsor
OccuLogix (Industry)
Overall Status
Suspended
CT.gov ID
NCT00460967
Collaborator
(none)
325
39
2
35
8.3
0.2

Study Details

Study Description

Brief Summary

SUMMARY

Age-related macular degeneration (AMD) is the leading cause of late onset visual impairment and legal blindness in people 65 years of age or older in the United States. It is a heterogeneous clinical entity in which retinal degeneration occurs predominantly in the macula in the context of aging and leads to impairment primarily of central visual acuity. The degenerative retinal eye disease occurs in two forms - a non-exudative "dry" form and an exudative "wet" form which in an individual patient may also represent stages of the disease. Non-exudative AMD accounts for 80-90% of AMD cases and it involves a constellation of clinical features that can include drusen, pigment clumping and/or retinal pigment epithelium (RPE) dropout, and geographic atrophy. Because of the overwhelming numbers of "dry" AMD subjects, the cumulative impact of this vision loss is significant.

There is no effective therapy for maintaining or improving vision associated with dry AMD. The only therapy for persons with dry AMD is an oral supplement containing high doses of antioxidants and zinc, which was tested by the National Eye Institute in a large, multi-center, double-masked, sham-controlled clinical trial1. This antioxidant therapy was shown to modestly retard the progression of dry AMD from an intermediate stage to the advanced stages and confirmed the benefit of antioxidant therapy in this disease. There is currently no FDA-approved therapy for the treatment of subjects with dry AMD.

Recently, the MIRA-1 modified per protocol population showed the effectiveness of Rheopheresis which is an application of selective therapeutic apheresis, namely double filtration plasmapheresis (DFPP) using a specifically designed filter for plasma filtration in subjects with non-exudative AMD. At one year the study reported with statistical significance (1) approximately a one line vision improvement in the Rheopheresis group versus no change in the Sham group and (2) 28% of subjects randomized to the active treatment gaining at least one line vision versus only 9% of subjects randomized to the sham treatment.

With a total of 300 subjects with dry AMD and visual acuity of 20/40-20/100 inclusive, the current investigation plans to prove the effectiveness of the Rheopheresis treatment on a larger scale. Each subject will receive a series of 8 treatments (either active treatment or sham treatment in a 2:1 ratio) for a period of approximately 2.5 months. In addition, a post-treatment ophthalmic evaluation will be performed 2 weeks after the 8th treatment (approximately 3 months after the baseline visit) and at the 6, 9 and 12 month visits. Comparing the one-year proportions of at least a 10-letter gain in ETDRS LogMar BCVA from baseline, the current investigation will show the effectiveness of Rheopheresis treatment (compared to sham treatment) for treating dry AMD subjects. Other secondary effectiveness endpoints, including mean changes and proportions of BCVA better than 20/40 at one year, will be analyzed to support the main investigation.

Condition or Disease Intervention/Treatment Phase
  • Device: Rheopheresis
  • Device: Rheopheresis
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
325 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Safety and Effectiveness, in a Multi-Center, Randomized, Sham Controlled Investigation for Dry, Non-Exudative Age Related Macular Degeneration (AMD)Using Rheopheresis
Study Start Date :
Jan 1, 2007
Anticipated Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Rheopheresis treatment

Device: Rheopheresis
8 rheopheresis treatments over 10 wks.

Sham Comparator: 2

Sham treatment

Device: Rheopheresis
Sham treatment

Outcome Measures

Primary Outcome Measures

  1. BCVA (Best Corrected Visual Acuity) [12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Study eye must have a diagnosis of non-exudative, "Dry", AMD with equivalent drusen surface area of approximately 31,000 µm2 [e.g. at least 10 soft, semi-soft intermediate size ≥63µm or at least 3 drusen size ≥125 µm within 3,000 µm of the fovea documented on macular exam, retinal angiography and fundus photographs as determined by the reading center. ETDRS BCVA of 20/40 - 20/100 inclusive
Exclusion Criteria:
  • Either eye with previous or active sub-retinal neovascularization (SRNV) or choroidal neovascularization (CNV)

  • Pigment epithelial detachment (PED) within 500 µm of the fovea

  • Either eye with a diagnosis of exudative (wet) AMD

  • Subjects having undergone cataract surgery less than 3 months prior to enrollment without an open posterior capsule

  • Uncontrolled hypertension and/or diabetes

  • Subjects with prolonged PT/PTT (unless the subject is taking warfarin), hematocrit <35%, evidence of active bleeding, platelet count <100,000/ml

Contacts and Locations

Locations

Site City State Country Postal Code
1 Retinal Consultants of Arizona Phoenix Arizona United States 85014
2 Associated Retina Consultants, LTD. Phoenix Arizona United States 85020
3 Mayo Clinic Hospital Phoenix Arizona United States 85054
4 Mayo Clinic, Department of Ophthalmology Scottsdale Arizona United States 85259
5 Southwest Kidney Institute, PLC, 2149 East Warner Rd. Ste. 109 & 110 Tempe Arizona United States 85284
6 Retina-Vitreous Associates Medical Group Beverly Hills California United States 90211
7 Good Samaritan Hospital Los Angeles California United States 90017
8 DSI Brandon Florida United States 33511
9 Center for Retina and Macular Disease Winter Haven Florida United States 33880
10 University of Illinois at Chicago Chicago Illinois United States 60612-7315
11 University of Illinois at Chicago Chicago Illinois United States 60612
12 University of Chicago Chicago Illinois United States 60637
13 Retina Group of Washington Chevy Chase Maryland United States 20815
14 Vitreo-Retinal Associates Worcester Massachusetts United States 01605
15 University of Massachuesettes Medical Health Center Worcester Massachusetts United States 01655
16 Retinovitreous Associates, Ltd. Cherry Hill New Jersey United States 08002
17 Ophthalmic Consultants of Long Island Lynbrook New York United States 11563
18 New York Blood Center New York New York United States 10021-6275
19 Macula Care New York New York United States 10021
20 Vitreous Retina Macula Consultants New York New York United States 10022
21 Columbia University New York New York United States 10032
22 Retina Associates of Cleveland Beachwood Ohio United States 44122
23 Cleveland Clinic Foundation, Cole Eye Institute Cleveland Ohio United States 44195
24 The Cleveland Clinic Cleveland Ohio United States 44195
25 Retina Associates of Cleveland Lakewood Ohio United States 44107
26 University of Pennsylvannia Medical Center Philadelphia Pennsylvania United States 19104
27 Texas Retina Associates Dallas Texas United States 75231
28 UT Southwestern Medical Center Dallas Texas United States 75390-9073
29 Memorial Hermann University of Texas Health Science Center Houston Texas United States 77030
30 The Methodist Hospital System Houston Texas United States 77030
31 Vitreoretinal Consultants Houston Texas United States 77030
32 Fairfax Pathology Associates, Ltd. Annadale Virginia United States 22003
33 Retina Group of Washington Fairfax Virginia United States 22031
34 Capital Health Systems, Ophthalmology & Visual Sciences Halifax Nova Scotia Canada B3H 2Y9
35 Victoria General Hospital Halifax Nova Scotia Canada B3H 2Y9
36 eyeMD Institute Brampton Ontario Canada L6V 1C2
37 Dr. Sapir Oakville Ontario Canada L6J 3P1
38 Rheopheresis Center Cologne Cologne Germany D-50674
39 University of Cologne Cologne Germany

Sponsors and Collaborators

  • OccuLogix

Investigators

  • Study Director: Nozhat Choudry, PhD, OccuLogix, Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00460967
Other Study ID Numbers:
  • RHEO-AMD 01-06
First Posted:
Apr 17, 2007
Last Update Posted:
Nov 7, 2007
Last Verified:
Apr 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 7, 2007