Phase 3
N=396
Efficacy and Safety of Ranibizumab (Intravitreal Injections) in Patients With Visual Impairment Due to Diabetic Macular Edema
Diabetic Macular Edema
Bottom Line
View on ClinicalTrials.gov: NCT00989989 ↗Enrolled (actual)
396
Serious AEs
15.8%
Results posted
Oct 2012
Primary outcome: Primary: Average Change From Baseline of Best-Corrected Visual Acuity (BCVA) Over 12 Months (From Month 1 to Month 12 Compared to Baseline) — 5.7; 5.9; 1.4 Letters
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Ranibizumab (Drug); Laser photocoagulation (Procedure); Sham ranibizumab (Drug); Sham laser photocoagulation (Procedure)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Novartis
- Primary completion
- Aug 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Average Change From Baseline of Best-Corrected Visual Acuity (BCVA) Over 12 Months (From Month 1 to Month 12 Compared to Baseline) |
5.7; 5.9; 1.4 | — |
| SECONDARY Change From Baseline on Central Retinal Subfield Thickness (CRST) at Month 12 |
-171.8; -134.6; -57.2 | — |
| SECONDARY Percent of Participants With Anatomical Changes in Intra-retinal Cysts at End of Study Compared to Baseline |
19.5; 21.8; 6.5; 40.3; 42.3; 35.1 | — |
| SECONDARY Percent of Participants With Anatomical Changes in Sub-retinal Fluid at End of Study Compared to Baseline |
13.6; 33.3; 25.0; 18.2; 11.1; 18.8 | — |
| SECONDARY Percent of Participants With Visual Acuity Above 73 Letters at Month 12 |
20.5; 16.5; 8.5 | — |
| SECONDARY Percent of Participants Who Gained >= 10 Letters at Month 12 Compared to Baseline |
37.2; 33.8; 13.3 | — |
| SECONDARY Percent of Participants Who Lost >= 10 Letters at Month 12 Compared to Baseline |
5.4; 3.0; 6.3 | — |
| SECONDARY Percent of Participants Who Gained >= 15 Letters at Month 12 Compared to Baseline |
17.8; 18.8; 7.8 | — |
| SECONDARY Percent of Participants Who Lost >= 15 Letters at Month 12 Compared to Baseline |
3.9; 1.5; 3.9 | — |
| SECONDARY Best-Corrected Visual Acuity (BCVA) Mean Change From Baseline at Month 12 |
6.4; 6.6; 1.8 | — |
| SECONDARY Patient Outcome Measure Euro Quality of Life Questionnaire (EQ-5D) |
2.8; -1.1; 1.0 | — |
Summary
This study was designed to confirm the efficacy and safety of ranibizumab (0.5 mg) as adjunctive therapy when added to laser photocoagulation and/or as monotherapy in Asian patients with visual impairment due to Diabetic Macular Edema (DME).
Eligibility Criteria
Inclusion Criteria
- Patients with Type 1 or Type 2 diabetes mellitus according to American Diabetes Association (ADA) or World Health Organization (WHO) guidelines with HbA1c not more than 10.0% at screening (Visit 1). Patients should be on diet, exercise, and/or pharmacological treatment for diabetes.
- Patients with visual impairment due to focal or diffuse Diabetic Macular Edema in at least one eye who are eligible for laser treatment in the opinion of the investigator. If both eyes are eligible, the one with the worse visual acuity, as assessed at Visit 1, will be selected for study treatment unless, based on medical reasons, the investigator deems the other eye the more appropriate candidate for study treatment.
- The study eye must fulfill the following criteria at Visit 1:
- Best-Corrected Visual Acuity (BCVA) score between 78 and 39 letters, inclusively, using Early Treatment of Diabetic Retinopathy (ETDRS) chart-like visual acuity testing charts at a testing distance of 4 meters (approximate Snellen equivalent of 20/32 to 20/160).
- Decrease in vision is due to DME and not due to other causes, in the opinion of the investigator.
- Medication for the management of diabetes must have been stable within 3 months prior to randomization and is expected to remain stable during the course of the study.
Exclusion Criteria
- Ocular concomitant conditions/ diseases:
- Concomitant conditions in the study eye which could, in the opinion of the investigator, prevent the improvement of visual acuity on study treatment.
- Active intraocular inflammation in either eye.
- Any active infection in either eye.
- History of uveitis in either eye.
- Uncontrolled glaucoma in either eye.
- Ocular treatments:
- Panretinal laser photocoagulation in the study eye within 6 months prior to or during the study.
- Focal/grid laser photocoagulation in the study eye within 3 months prior to study entry.
- Systemic conditions or treatments:
- History of stroke
- Renal failure requiring dialysis or renal transplant or renal insufficiency with creatinine level > 2.0 mg/dL.
- Untreated diabetes mellitus
- Blood pressure systolic > 160 mmHg or diastolic > 100 mmHg
- Compliance/ Administrative:
- Pregnant or nursing (lactating) women
Other protocol-defined inclusion/exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT00989989). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.