Canadian Treat and Extend Analysis Trial With Ranibizumab
- Conditions
- wetAMD
- Interventions
- Other: 0.5 mg Ranibizumab intravitreal injections
- Registration Number
- NCT02103738
- Lead Sponsor
- Novartis Pharmaceuticals
- Brief Summary
This is an observational study to will evaluate and compare two Ranibizumab treatment regimens (Standard of care) in patients with neovascular (wet) age-related macular degeneration (wAMD) aiming to achieve and to maintain a maximum visual function benefit. The results will be used to generate further recommendations on the timing of treatment administration for patients with neovascular (wet) age-related macular degeneration (wAMD). In this context, the study will use the anatomical imaging (for example, optical coherence tomography \[OCT\]) to evaluate wAMD disease activity impacted by the recurrence of disease instability and for decision making in the treatment decision algorithm.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 505
- Infomed consent,
- Male and Female, 50 years of age or older
- Diagnosis of treatment-naive CNV secondary to age-related macular degeneration(AMD) in the study eye,
- BCVA score between 78 and 19 letters inclusive,
- Patients with structural foveal damage in the study eye,
- Patients with confounding severe oculare diseases,
- Patients with suspicion of ( Polypoidal Choroidal Vasculapathy PCV) in the study eye,
- Patients with active or suspected or periocular infections in either eye or active intraocular inflammation in either eye,
- Patients who had previous subfoveal laser photocoagulation in the study eye or history of vitrectomy surgery in the study eye,
- Patients who had any prior treatment in the study eye, e.g., with Visudyne*, Avastin*, prior Ranibizumab treatment, Ozurdex*, external radiation therapy, transpupillary thermotherapy (TTT), or any intravitreal injection,
- Patients with a known sensitivity to Ranibizumab or any component of its formulation,
- Patients who have used any investigational agent in the last 30 days,
- Concurrent participation in a clinical trial or within 30 days prior to enrollment,
- Patients having received systemic treatment with any other anti-vascular endothelial growth factor (VEGF) therapy ≤ 60 days prior to enrollment
- Patients with physical or mental disabilities that prevent accurate vision testing,
- Patients physically unable to tolerate intravenous fluorescein angiography,
- Pregnant or breastfeeding female patients,
- Any patient with recent history of new onset cardiac disease or thromboembolic central nervous system (CNS) event (within 12 months of Baseline Visit),
- Patients with any other condition which, in the opinion of the Investigator, would require treatment that would significantly impact the treatment assessments during this study.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Arm 1 (Monthly) 0.5 mg Ranibizumab intravitreal injections 0.5 mg intravitreal injections of Ranibizumab monthly for the duration of the study. Arm 2 (Treat and Extend) 0.5 mg Ranibizumab intravitreal injections Three consecutive months of 0.5 mg Ranibizumab intravitreal injections (Day 1, Month 1, and Month 2). Monthly injections will continue until evidence of disease stability is observed. Specifically, monthly treatment will continue until visual acuity is deemed stable as indicated by a gain in visual acuity of ≤ 3 ETDRS letters from the prior month, no clinical evidence of lesion growth, fluid or blood, and no intraretinal or subretinal fluid on OCT. When this is achieved, the intervals between each subsequent injection will be extended by 2 weeks (intervals of 6 weeks, 8 weeks, 10 weeks, to a maximum of 12 weeks) until clinical or diagnostic evidence of disease instability is observed based on OCT findings and/or BCVA ETDRS.
- Primary Outcome Measures
Name Time Method Mean Change in Visual Acuity Baseline to Month 12 Visual Acuity (VA) will be assessed using best correction determined from protocol refraction during screening and every 3 months throughout the study; in the monthly regimen and during screening and at every visit thereafter throughout the study in the treat and extend regimen. VA measurements (number of letters correctly identified) will be performed with the patient in a sitting position using Early Treatment Diabetic Retinopathy Study (ETDRS)-like VA testing charts at an initial testing distance of 4 meters. This outcome measure will describe the difference in the VA mean changes between the two regimens from Baseline to Month 12.
- Secondary Outcome Measures
Name Time Method Proportion of patients with a loss of less than 5, 10, and 15 letters between the 2 treatment arms. baseline to Month 24 Mean change in BCVA ETDRS between the 2 treatment arms at Month 12 compared to Month 3. Month 12 and Month 3 Mean change in BCVA ETDRS between the 2 treatment arms. Baseline to Month 24 Proportion of patients with a gain of equal or more than 5, 10, and 15 letters between the 2 treatment arms. Baseline to Month 24 Proportion of patients with a loss of less than 5, 10, and 15 letters between the 2 treatment arms from baseline to Month 12 and from baseline to Month 24. baseline to Month 12 Number of injections performed in each treatment arms. Month 12 to Month 24
Trial Locations
- Locations (1)
Novartis Investigative Site
🇨🇦Thetford Mines, Quebec, Canada