Post Marketing Study to Evaluate the Safety and Effectiveness of Brolucizumab in Patients With Diabetic Macular Edema.
Study Details
Study Description
Brief Summary
The purpose of this study is to generate additional safety and effectiveness data in Indian Diabetic macular edema (DME) patients that more closely resemble the real-world population intended to be treated with Brolucizumab. This study is being conducted as part of the post-marketing regulatory commitment to the Indian Health authority.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
This study is a prospective, non-interventional, open-label, single-arm, multi-center phase IV study to evaluate safety and effectiveness of intravitreal injections (IVI) of brolucizumab in patients with diabetic macular edema (DME) for whom a decision has already been made to be treated with brolucizumab, irrespective of the trial participation. The study period for each patient will be 40 weeks from the informed consent and enrolment in the study.
Assessments/investigations shall be performed in accordance to the local clinical practice and the Investigator's assessed response will be collected in the database. Any patient who suffers from intraocular inflammation (IOI) during the study, treatment with brolucizumab will be discontinued.
Data originating from assessments and evaluations performed at routine patient visits will be collected from the patient's medical records at Baseline, i.e., the start of brolucizumab treatment, and approximately at Week 6, Week 12, Week 18, Week 24, Week 32, Week 36, and at Week 40. Safety data (AEs and SAEs) from any time point during the duration of the study.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| brolucizumab 6 mg brolucizumab 6 mg intravitreal injection |
Other: brolucizumab
There is no treatment allocation. Treatment with brolucizumab 6 mg intravitreal injection will be based on the local label/clinical practice.
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Outcome Measures
Primary Outcome Measures
- Incidence and characteristics of treatment-emergent adverse events during the 40 weeks of treatment with Brolucizumab. [40 weeks]
To evaluate ocular & non-ocular safety of intravitreal brolucizumab in real-world patients with Diabetic Macular Edema (DME).
Secondary Outcome Measures
- Mean change in BCVA from Baseline to Week 40 as measured by ETDRS letters. [Baseline, week 40]
To evaluate the effectiveness of brolucizumab in the management of DME in terms of change in best-corrected visual acuity (BCVA) from Baseline to Week 40 as measured by Early Treatment Diabetic Retinopathy Study (ETDRS) letters. Min and max possible scores are 0-100 letters read respectively. A higher score represents better visual functioning.
- Percentage of patients with presence/absence of IRF and SRF at Week 40 compared to Baseline. [Baseline, week 40]
To evaluate the effectiveness of brolucizumab on fluid [intraretinal fluid (IRF) and subretinal fluid (SRF)] from Baseline to Week 40.
- Mean change in CRT as assessed by Optical Coherence Tomography (OCT) from Baseline to Week 40. [Baseline, week 40]
To evaluate the effectiveness of brolucizumab on central retinal thickness (CRT) from Baseline to Week 40.
- Number of brolucizumab injections administered to the patients during 40 weeks of treatment with brolucizumab. [40 weeks]
To characterize the number of anti-VEGF injections during the 40 weeks of treatment with brolucizumab in the study.
- Number of non-injection visits during 40 weeks of treatment with brolucizumab. [40 weeks]
To characterize the number of non-injection visits during the 40 weeks of treatment with brolucizumab in the study.
- Total number of visits during 40 weeks of treatment with brolucizumab. [40 weeks]
To characterize the total number of visits during the 40 weeks of treatment with brolucizumab in the study.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male and female patients ≥ 18 years old with visual impairment due to DME involving the center of the macula.
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Patients with type 1 or type 2 diabetes mellitus.
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Patient or legally acceptable representative (LAR) must provide signed informed consent for participation in the study.
Exclusion Criteria:
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Concomitant conditions or ocular disorders in the study eye at screening or Baseline which could, in the opinion of the Investigator, prevent response to study treatment or may confound interpretation of study results, compromise visual acuity or require medical or surgical intervention during the study period (e.g., cataract, vitreous hemorrhage, retinal vascular occlusion, retinal detachment, macular hole, or choroidal neovascularization of any cause).
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Patient with existing or suspected ocular or periocular infection in the study eye.
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Patient with an existing intraocular inflammation (IOI) in the study eye.
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Patient who has undergone intraocular surgery including laser photocoagulation in the study eye within 3 months prior to enrollment in this study.
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Patient with uncontrolled glaucoma defined as intraocular pressure > 25 mmHg despite treatment with anti-glaucoma medication, or according to Investigator's judgment.
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Patient having scar, fibrosis, and atrophy involving the center of the fovea in the study eye.
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Active proliferative diabetic retinopathy in the study eye as per Investigator.
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Patient having history of cardiac or cerebral ischemia in last 6 months prior to enrollment in this study.
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Previous treatment with any anti-VEGF drugs, steroids (dexamethasone intravitreal implant or triamcinolone acetonide) or other investigational drugs in the study eye.
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Pregnant or nursing (lactating) women at screening, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG pregnancy test.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Novartis Pharmaceuticals
Investigators
- Study Director: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CRTH258BIN01