Dorzolamide-timolol in Combination With Anti-vascular Endothelial Growth Factor Injections for Wet Age-related Macular Degeneration

Neovascular Age-related Macular Degeneration Clinical Trial

— DAWN  

Official title:

A Randomized Controlled Trial Comparing the Effect of Topical Dorzolamide-Timolol Versus Placebo Combined With Intravitreal Anti-Vascular Endothelial Growth Factor (VEGF) Injections in Patients With Neovascular Age-Related Macular Degeneration Who Are Incomplete Anti-VEGF Responders

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03034772
• Other study ID #: 16-596
• Status: Completed
• Phase: Phase 2/Phase 3
• Start date: February 8, 2017
• Est. completion date: July 5, 2019

Study information

• Verified date: June 2020
• Source: Wills Eye
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A previous pilot study demonstrated that commonly available glaucoma drops (dorzolamide-timolol) might decrease the amount of chronic swelling in patient with wet age-related macular degeneration who have been receiving anti-vascular endothelial growth factor (VEGF) injections. This will be a larger study where subjects are randomly assigned to receive the glaucoma drops or a placebo (artificial tears) in order to confirm whether this previous finding is valid. Subjects will continue to receive the normally scheduled anti-VEGF injections at regular intervals as done prior to enrollment. The only addition to the regimen will be the daily use of eye drops (dorzolamide-timolol or artificial tears) twice daily for the duration of the study. At the end of the study, the swelling in the retina will be compared to the amount before starting the drops to see if there is any difference between the group using dorzolamide-timolol versus artificial tears.

Description:

Intravitreal anti-vascular endothelial growth factor (VEGF) agents, including ranibizumab and aflibercept, remain the standard of care treatment for neovascular age-related macular degeneration (AMD). Various treatment modalities using these agents have been proposed, including monthly, pro re nata, and treat-and-extend regimens. Despite frequent and consistent treatment with anti-VEGF therapy, there is a subset of patients who are incomplete responders and have persistent exudation, including intraretinal edema, subretinal fluid (SRF), and/or retinal pigment epithelial detachment (PED) on spectral-domain optical coherence tomography (SD-OCT). While clearance of intravitreal anti-VEGF drugs is not completely understood, some studies have suggested that outflow through the anterior chamber may play a role. We hypothesized that by decreasing aqueous production, outflow may also be reduced which could subsequently slow the clearance of intravitreal drugs. In a prior pilot study with 10 eyes of 10 patients who were incomplete responders with neovascular AMD, the effect of topical dorzolamide-timolol in combination with continued intravitreal anti-VEGF injections was explored. Patients were kept on the same anti-VEGF drug as well as the same interval between injections for the 2 visits before enrollment and through the course of the pilot study in order to minimize the chances that any changes noted might be the result of altering one of these variables. The mean central subfield thickness (CST) decreased from 419.7 μm at enrollment to 334.1 μm at the final visit (p=0.012). Mean maximum subretinal fluid (SRF) height decreased from 126.6 μm at enrollment to 56.5 μm at the final visit (p=0.020). This decrease in mean CST and SRF was significant beginning at the first visit after initiation of the drops. Based on this initial pilot data, dorzolamide-timolol appears to be a promising adjuvant treatment in combination with anti-VEGF injections for incomplete anti-VEGF responders with neovascular AMD. However, since there was no control group in the pilot study, it is possible that the decreased exudation seen was a result of the continued anti-VEGF therapy alone rather than an effect of the topical therapy. As a result, a randomized, placebo-controlled clinical trial will be better able to assess the efficacy of dorzolamide-timolol in this setting.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: July 5, 2019
• Est. primary completion date: February 8, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years and older

Eligibility

Inclusion Criteria:

1. Active choroidal neovascularization (CNV) due to AMD.

2. Prior treatment with at least 4 injections of anti-VEGF agents in the past 6 months and persistent intraretinal and/or subretinal fluid on SD-OCT at each visit during this period.

3. Baseline CST = 270 µm on SD-OCT automated retinal thickness map.

4. Injection of the same anti-VEGF agent at each of the two visits immediately preceding study enrollment.

5. Time interval of 5 weeks (± 1 week) between visits for at least two visits immediately preceding study enrollment.

6. Subjects of either gender aged = 45 years.

7. Provide written informed consent

8. Ability to comply with study and follow-up procedures and return for study visits.

Exclusion Criteria:

1. History of uveitis.

2. Presence of intraocular inflammation, significant epiretinal membrane (causing distortion of macular anatomy per investigator discretion), significant vitreomacular traction (per investigator discretion), macular hole, or vitreous hemorrhage.

3. Any ophthalmic surgery within previous 6 months, including cataract extraction.

4. Any history of vitrectomy or glaucoma surgery (e.g., trabeculectomy, tube shunt).

5. Current prescription eye drop usage (e.g., glaucoma drops, corticosteroid drops, etc.).

6. Any contraindication for topical use of a beta-blocker (e.g., bradycardia, decompensated heart failure, chronic obstructive pulmonary disease, reactive airway disease, asthma, etc.).

7. Any history of sulfonamide allergy.

Related Conditions & MeSH terms

• Macular Degeneration
• Neovascular Age-related Macular Degeneration
• Wet Macular Degeneration

Intervention

Drug:
• Dorzolamide-timolol
Topical eye drop (active comparator) used twice daily for study duration

Other:
• Artificial tears
Topical eye drop (placebo comparator) used twice daily for study duration

Locations

Country	Name	City	State
United States	Ophthalmic Consultants of Boston	Boston	Massachusetts
United States	Retina Consultants of Houston	Houston	Texas
United States	Palo Alto Medical Foundation	Palo Alto	California
United States	Mid Atlantic Retina- Wills Eye Institute	Philadelphia	Pennsylvania
United States	Associated Retinal Consultants	Royal Oak	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
Wills Eye	Mid Atlantic Retina

Country where clinical trial is conducted

United States, 

References & Publications (1)

Sridhar J, Hsu J, Shahlaee A, Garg SJ, Spirn MJ, Fineman MS, Vander J. Topical Dorzolamide-Timolol With Intravitreous Anti-Vascular Endothelial Growth Factor for Neovascular Age-Related Macular Degeneration. JAMA Ophthalmol. 2016 Apr;134(4):437-43. doi: 10.1001/jamaophthalmol.2016.0045. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Mean Central Subfield Thickness (CST)	Change in mean CST on spectral domain optical coherence tomography from baseline to the final visit	Baseline and 18 weeks
Secondary	Change in Mean Maximum Subretinal Fluid (SRF) Height	Change in mean maximum SRF height on spectral domain optical coherence tomography from baseline to final visit.	Baseline and 18 weeks
Secondary	Change in Mean Maximum Pigment Epithelial Detachment (PED) Height	Change in mean maximum PED height on spectral domain optical coherence tomography from baseline to final visit.	Baseline and 18 weeks
Secondary	Change in Visual Acuity	Change in mean best available visual acuity from baseline to final visit.	Baseline and 18 weeks
Secondary	Change in Mean Intraocular Pressure (IOP)	Change in mean IOP from baseline to final visit.	Baseline and 18 weeks