The READ-2 Study: Ranibizumab for Edema of the mAcula in Diabetes

Diabetic Macular Edema Clinical Trial

Official title:

Ranibizumab for Edema of the Macula in Diabetes: a Phase 2 Study ( The Read-2 Study)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00407381
• Other study ID #: NA_00005254
• Status: Active, not recruiting
• Phase: Phase 2
• First received: December 1, 2006
• Last updated: January 30, 2009
• Start date: December 2006
• Est. completion date: December 2009

Study information

• Verified date: January 2009
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This study is being done to see if the investigational drug Ranibizumab (RBZ) given by injection into the eye, is safe and effective to use in people with diabetic macular edema (DME). The investigators want to compare RBZ to laser treatment which is the current standard way to treat DME.

RBZ blocks a growth factor that is thought to be involved in the formation of abnormal blood vessels that cause loss of vision in patients with DME.

Description:

The READ-2 Study is a phase 2 randomized, multi-center clinical trial to be conducted under an investigator-initiated IND. The study aims to enroll 126 patients, who will be randomized into 3 different groups. The primary objectives of the READ-2 Study are: (a) to obtain data on the bioactivity and dose interval effects of intravitreal ranibizumab (RBZ) alone, as well as in combination with laser photocoagulation, on retinal thickness and visual acuity in subjects with DME; and (b) to obtain additional safety and bioactivity data to aid in the design of a phase 3 clinical trial to evaluate ranibizumab as a therapeutic option for patients with DME The study consists of a 2-week screening period (Days -14 to 0), a 6-month treatment period with a primary time endpoint, and a 18-month follow-up and treatment period with secondary time endpoints. Consented subjects will enter the 14-day screening period to determine eligibility. Serum chemistry and hematology testing, urinalysis, pregnancy testing, and macular thickness measurements based on optical coherence tomography (OCT) will be performed. Screening will also include VA, ophthalmic examination and FA entry criteria.

Patients who have ETDRS visual acuity of 20/40 or worse, but better than or equal to 20/320 due to foveal thickening from macular edema secondary to diabetes (type 1 or 2) and who meet eligibility criteria will be eligible to enroll in the study. Baseline foveal thickness by OCT must be at least 250, which is often associated with VA of 20/40 or worse and which provides sufficient thickening so that a treatment effect is easily detectable (Nguyen et al. 2004). Approximately 126 patients with DME will be enrolled in this study from all clinical sites in the study. Every effort will be made to recruit and enroll eligible patients from men and women of all ethnic and social backgrounds. Patients who meet entry criteria will be able to enroll in the study until the quota of patients has been achieved.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 126
• Est. completion date: December 2009
• Est. primary completion date: December 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion:

• Signed informed consent and authorization of use and disclosure of protected health information

• Age greater than 18 years

• Diagnosis of diabetes mellitus (type 1 or type 2) and serum HbA1c greater than 5.5% within 12 months of randomization

• Retinal thickening secondary to diabetes mellitus (diabetic macular edema) involving the center of the fovea.

• Diagnosis must be confirmed by OCT images

• Foveal thickness of greter than 250, as assessed by OCT

• Best corrected visual acuity score in the study eye of 20/40 to 20/320 inclusive (Snellen equivalents using the ETDRS protocol at a distance of 4 meters). Only one eye will be treated in the study. If both eyes are eligible, the investigator will select the eye to be enrolled. Visual acuity in the non-study eye must be greater than 20/800.

• In the opinion of the investigator, decreased vision in the study eye is due to foveal thickening from DME and not from other obvious causes.

• In the opinion of the investigator, laser photocoagulation can be withheld for at least 30 days after the patient has enrolled in the study

Exclusion Criteria:

• Panretinal photocoagulation or macular photocoagulation within 3 months of study entry in the study eye

• Use of intraocular or periocular injection of steroids in the study eye (e.g., triamcinolone) within 3 months of study entry

• Previous participation in a study and receipt of anti-angiogenic drugs (pegaptanib sodium, ranibizumab, anecortave acetate, protein kinase C inhibitor, etc.) within 2 months of study entry

• Eyes in which the investigators do not feel appropriate to do any additional laser photocoagulation

• Proliferative diabetic retinopathy in the study eye, with the exceptions of inactive, fibrotic proliferative diabetic retinopathy that has regressed following pan-retinal laser photocoagulation or tufts of NVE less than one disc area with no vitreous hemorrhage

• Vitreomacular traction or epiretinal membrane in the study eye evident biomicroscopically or by OCT

• Structural damage to the center of the macula in the study eye likely to preclude improvement in visual acuity following the resolution of macular edema, including atrophy of the retinal pigment epithelium, subretinal fibrosis, laser scar(s), macular ischemia, or organized hard exudate plaque

• Ocular disorders in the study eye that may confound interpretation of study results, including retinal vascular occlusion, retinal detachment, macular hole, or choroidal neovascularization of any cause (e.g., AMD, ocular histoplasmosis, or pathologic myopia)

• Concurrent disease in the study eye that could compromise visual acuity or require medical or surgical intervention during the first 6-month study period

• Eyes which are likely to need cataract surgery and intraocular lens implantation within the first 6 months of the study

• Cataract surgery in the study eye within 3 months of study entry; Yttrium-Aluminum-Garnet (YAG) laser capsulotomy within 2 months of study entry; or any other intraocular surgery within 3 months preceding Day 0.

• History of vitreoretinal surgery in the study eye within 3 months of study entry

• Uncontrolled glaucoma (defined as intraocular pressure greater than 30 mm Hg despite treatment with anti-glaucoma medications)

• Uncontrolled diabetes mellitus, as evidenced by glycosylated hemoglobin (HbA1c) value greater than 12%

• Premenopausal women not using adequate contraception

• Any women who are pregnant

• INR greater than or equal to 3.0 (e.g. due to current treatment with warfarin). The use of aspirin or other anticoagulants is not an exclusion

• History of gastrointestinal bleeding within 2 months of study enrollment

• History of major gastrointestinal, cardiothoracic, gynecological, genitourinary, or orthopedic surgeries within 2 months of study enrollment

• History of cerebral vascular accident, myocardial infarction, transient ischemic attacks within 6 months of study enrollment

• Any patients who are on renal dialysis

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetic Macular Edema
• Edema
• Macular Edema

Intervention

Drug:
• Ranibizumab
Ranibizumab for intravitreal injection. .05ml dosing at 30 day intervals and PRN with dosing criteria.

Procedure:
• Laser photocoagulation
Laser photocoagulation in either focal or grid pattern as determined by investigator.

Locations

Country	Name	City	State
United States	University of New Mexico	Albuquerque	New Mexico
United States	Emory University	Atlanta	Georgia
United States	Wilmer Eye Institute at Johns Hopkins University School of Medicine	Baltimore	Maryland
United States	Retina-Vitreous Associates Medical Group	Beverly Hills	California
United States	Ophthalmic Consultants of Boston	Boston	Massachusetts
United States	Illinois Retina Associates Rush University	Chicago	Illinois
United States	University of Chicago	Chicago	Illinois
United States	Duke Eye Center	Durham	North Carolina
United States	Midwest Eye Institute	Indianapolis	Indiana
United States	Eye Care Specialists, PC	Kingston	Pennsylvania
United States	Retinal Consultants of Nevada	Las Vegas	Nevada
United States	University of Southern California	Los Angeles	California
United States	Yale Eye Center	New Haven	Connecticut
United States	East Bay Retina Consultants	Oakland	California
United States	Retina Institute of California	Pasadena	California
United States	Retinal Consultants of Arizona	Phoenix	Arizona
United States	Southern New England Retina Associates	Providence	Rhode Island
United States	Black Hills Regional Eye Institute	Rapid City	South Dakota
United States	University of California, San Francisco	San Francisco	California
United States	New England Retina Consultants, PC	West Springfield	Massachusetts

Sponsors (3)

Lead Sponsor	Collaborator
Johns Hopkins University	Genentech, Inc., Juvenile Diabetes Research Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Improvement in vision of 15 or more letters, or achieve a final vision of 50 letters (20/25) or better if baseline VA was 40 letters (20/40)		6 mos, 12 mos and 24 mos. Study Extended to 36 mos.	Yes
Secondary	Several outcomes related to OCT measurements and fluorescein angiography.		6 mos, 12 mos and 24 mos, study extended to 36 mos.	Yes