@article{b50d60de575145c28178642110dd9718,
title = "Suprachoroidal CLS-TA for non-infectious uveitis: An open-label, safety trial (AZALEA)",
abstract = "PURPOSE: To evaluate local and systemic safety of suprachoroidal (SC) triamcinolone acetonide injectable suspension (CLS-TA) injections in subjects with non-infectious uveitis (NIU).DESIGN: Open-label, prospective multicentre safety study.PARTICIPANTS: Thirty-eight subjects with NIU, with and without macular oedema (MO).METHODS: Treatment consisted of two suprachoroidal injections of CLS-TA 4 mg, 12 weeks apart. Best-corrected visual acuity (BCVA), adverse event (AE) assessment, ophthalmic examinations and optical coherence tomography (OCT) were conducted every 4 weeks for 24 weeks. Blood samples were analysed for plasma triamcinolone acetonide (TA) concentrations.MAIN OUTCOME MEASURES: The main outcome measure was frequency of AEs. Other endpoints included plasma TA concentrations, change in signs of inflammation, BCVA and retinal central subfield thickness (CST).RESULTS: Based on a CST of >300 µm, 20 out of 38 subjects had MO at baseline. Mean intraocular pressure (IOP) was 13.3 mm Hg at baseline and 15.2 mm Hg at week 24 in the study eye. A total of six (15.8%) subjects had an IOP rise >10 mm Hg compared with baseline, in the study eye, and two (5.3%) subjects had IOP >30 mm Hg (maximum 34 mm Hg at week 8 and 38 mm Hg at week 20). Cataract formation AEs were reported in four study eyes; one of which was deemed treatment-related. No serious ocular AEs in the study eye occurred in the study. Quantifiable post-injection TA plasma concentration was <1 ng/mL. Efficacy parameters showed improvement over the 24-week study period.CONCLUSIONS: Suprachoroidally administered CLS-TA was safe and well tolerated over the 24-week, open-label study in NIU subjects with and without MO.",
keywords = "drugs, inflammation, intraocular pressure, retina, Prospective Studies, Uveitis/diagnosis, Glucocorticoids, Humans, Retina, Treatment Outcome, Eye Infections, Bacterial/drug therapy, Visual Acuity, Triamcinolone Acetonide, Macular Edema/drug therapy, Tomography, Optical Coherence/methods",
author = "Henry, {Christopher Ryan} and Milan Shah and Barakat, {Mark R.} and Pouya Dayani and Wang, {Robert C.} and Khurana, {Rahul N.} and Lana Rifkin and Steven Yeh and Colette Hall and Thomas Ciulla",
note = "Funding Information: 1Retina Consultants of Texas, Houston, Texas, USA 2Ophthalmology, Houston Methodist Hospital, Houston, Texas, USA 3Midwest Eye Institute, Indianapolis, Indiana, USA 4Retinal Consultants of Arizona, Phoenix, Arizona, USA 5Retina Vitreous Associates, Los Angeles, California, USA 6Texas Retina Associates, Dallas, Texas, USA 7Northern California Retina Vitreous Associates, Mountain View, California, USA 8Ophthalmology, University of California, San Francisco, California, USA 9Ophthalmic Consultants of Boston, Boston, Massachusetts, USA 10Ophthalmology, Emory Eye Center, Atlanta, Georgia, USA 11Clearside Biomedical Inc, Alpharetta, Georgia, USA 12Retina Service, Midwest Eye Institute, Indianapolis, Indiana, USA Correction notice This article has been corrected since it was published online. An error was introduced during the production process in the results section of the abstract. In the Abstract results, first sentence: {\textquoteright}Based on a CST of ≥300 µm, 20 out of 38 subjects had MO at baseline.{\textquoteright} has been changed to: {\textquoteright}Based on a CST of >300 µm, 20 out of 38 subjects had MO at baseline.{\textquoteright} Further, in the Abstract results, fourth sentence: {\textquoteright}Cataract formation AEs were reported in four study eyes; two of which were deemed treatment-related.{\textquoteright} should be: {\textquoteright}Cataract formation AEs were reported in four study eyes; one of which was deemed treatment-related.{\textquoteright} Twitter Thomas Ciulla @ThomasCiullaMD Contributors All coauthors contributed to the data acquisition and/or research execution, data analysis and/or interpretation, and manuscript preparation. Funding This study was funded by Clearside Biomedical (Alpharetta, Georgia, USA). The sponsor participated in the design of the study, conducting the study, data collection, data management, data analysis, interpretation of the data, preparation and review of the manuscript. Competing interests CRH reports receiving consulting fees from Clearside Biomedical and Bausch & Lomb. MS reports receiving grant support from Clearside Biomedical. MRB reports receiving consulting fees from Allegro, Allergan, Alimera, Bausch & Lomb, Genentech, Novartis and Regenxbio. RNK reports receiving consulting fees from Allergan, Clearside Biomedical, Genentech and Regeneron. He also reports receiving grant support from Allergan, Chengdu Kanghong, Clearside Biomedical, Roche and Santen. LR reports receiving consulting fees from Bausch & Lomb. SY reports receiving consulting fees from Clearside Biomedical and Santen. He also reports receiving grant funding from Clearside Biomedical. CH and TC are employees of Clearside Biomedical. Funding Information: CRH reports receiving consulting fees from Clearside Biomedical and Bausch & Lomb. MS reports receiving grant support from Clearside Biomedical. MRB reports receiving consulting fees from Allegro, Allergan, Alimera, Bausch & Lomb, Genentech, Novartis and Regenxbio. RNK reports receiving consulting fees from Allergan, Clearside Biomedical, Genentech and Regeneron. He also reports receiving grant support from Allergan, Chengdu Kanghong, Clearside Biomedical, Roche and Santen. LR reports receiving consulting fees from Bausch & Lomb. SY reports receiving consulting fees from Clearside Biomedical and Santen. He also reports receiving grant funding from Clearside Biomedical. CH and TC are employees of Clearside Biomedical. Publisher Copyright: {\textcopyright} 2022 BMJ Publishing Group. All rights reserved. {\textcopyright} Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.",
year = "2022",
month = jun,
day = "1",
doi = "10.1136/bjophthalmol-2020-318019",
language = "English (US)",
volume = "106",
pages = "802--806",
journal = "British Journal of Ophthalmology",
issn = "0007-1161",
publisher = "BMJ Publishing Group",
number = "6",
}