A phase IV study of Faricimab to explore associations of visual acuity benefits and changes in vascular integrity using adaptive optics in patients with diabetic macular edema
Trial Snapshot
- Phase
- Phase 4
- Status
- Recruiting
- Sponsor
- Enrollment
- 170
- Locations
- 1
- Primary Endpoint
- Improvement of visual acuity, measured by change in BCVA (metric variable). BCVA (as measured as letters on the ETDRS chart at a starting distance of 4 m) will be collected from each individual patients of group 1a and group 1b at baseline and at 12 months
Study Overview
Brief Summary
To prove efficacy of Faricimab treatment in BCVA improvement in two different patient populations with diabetic macular edema (in group 1a from baseline to at 12 months and group 1b from baseline to at 12 months).
Eligibility Criteria
- Ages
- 18 years to 65+ years (18-64 Years, 65+ Years)
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •signed informed consent
- •age ≥18 years, both sexes
- •HbA1c of ≤16%
- •best-corrected visual acuity (BCVA) in the study eye above >25 letters of Early Treatment Diabetic Retinopathy Study (ETDRS) nomenclature (corresponding to 1.2 VAlogMAR)
Exclusion Criteria
- •Pregnancy or breastfeeding
- •participation in any non-interventional or interventional study
- •previously treated with Faricimab, photodynamic therapy and/or macular laser therapy (photocoagulation)
- •visual acuity below 0.2 Snellen
- •glaucoma, intermediate and late age-related macular degeneration, uveitis
- •hypertensive retinopathy stage 3 and 4
Outcomes
Primary Outcomes
Improvement of visual acuity, measured by change in BCVA (metric variable). BCVA (as measured as letters on the ETDRS chart at a starting distance of 4 m) will be collected from each individual patients of group 1a and group 1b at baseline and at 12 months
Improvement of visual acuity, measured by change in BCVA (metric variable). BCVA (as measured as letters on the ETDRS chart at a starting distance of 4 m) will be collected from each individual patients of group 1a and group 1b at baseline and at 12 months
Secondary Outcomes
- Number of injections during the 12 months therapy on a Q4W, Q8W, Q12W, or Q16W treatment interval at 12 months
- To evaluate the efficacy of Faricimab on anatomical outcomes using SD-OCT as a clinically relevant parameter for the decision of the treat and extend scheme (T&E). Corresponding secondary endpoints: ● Change from baseline to at 12 months ● absence of DME (CST <325 μm) to at 12 months ● absence of IRF (intra-retinal fluid) to at 12 months ● absence of SRF (sub-retinal fluid) to at 12 months ● absence of IRF and SRF to at 12 months
- ● Change from baseline in BCVA over time ● gaining ≥10, ≥5, or ≥0 ETDRS letters in BCVA from at baseline to at 12 month ● avoiding a loss of ≥15, ≥10, or ≥5 ETDRS letters in BCVA from at baseline to at 12 month ● gaining ≥15 ETDRS letters from at baseline or achieving BCVA of ≥84 ETDRS letters to at 12 month
- ● BCVA Snellen equivalent of 20/40 (BCVA ≥69 ETDRS letters) or better to at 12 months ● BCVA Snellen equivalent of 20/200 (BCVA ≤38 ETDRS letters) or worse to at 12 months ● Improved vision measured by Adaptive Sensory Technology (AST) for contrast sensitivity and visual acuity
- ● longitudinal WLR measurements from at baseline (first visit) to at 12 months) ● gaining WLR >0.1 or >0.5 or <0.1 from at baseline to at 12 month ● Mean WLR at baseline in group 1a significant different from mean WLR at 12 months ● Mean WLR at baseline in group 1b significant different from mean WLR at 12 months
- ● Change from baseline in FAZ (in µm2) to at 12 months ● >10% reduction of the FAZ to at 12 month
- Quantification of countable area size in mm2 and photoreceptor density (cones per mm2) by AO at an edema border. ● Change of area size mm2 (focused countable cones per mm2 in a defined retinal area) from baseline to at 12 month ● Change from baseline of photoreceptor density (cones per mm2) to at 12 month
Investigators
Prof. Arne Viestenz
Scientific
Martin-Luther-Universitaet Halle-Wittenberg
