The suprachoroidal space (SCS) is a potential space located between the choroid and sclera. Medications can be injected into this space, using a microneedle, to allow for targeted and sustained delivery to the posterior segment with compartmentalization from unintended tissues such as the anterior segment.[1,2,3] Because the suprachoroidal space is adjacent to target structures within the eye, namely the retina and choroid, it provides a way to optimize the therapeutic effects while minimizing secondary complications.
Hancock SE, Wan CR, Fisher NE, Andino RV, Ciulla TA. Biomechanics of suprachoroidal drug delivery: from benchtop to clinical investigation in ocular therapies. Expert Opin Drug Deliv. 2021;18(6):777-788. doi:10.1080/17425247.2021.1867532
Patel SR, Lin AS, Edelhauser HF, Prausnitz MR. Suprachoroidal drug delivery to the back of the eye using hollow microneedles. Pharm Res. 2011;28:166-176.
Patel SR, Berezovsky DE, McCarey BE, Zarnitsyn V, Edelhauser HF, Prausnitz MR. Targeted administration into the suprachoroidal space using a microneedle for drug delivery to the posterior segment of the eye. Invest Ophthalmol Vis Sci. 2012;53(8):4433-4441. Published 2012 Jul 1.
The advent of CLS-TA (Xipere; Bausch + Lomb and Clearside Biomedical) demonstrated the safe delivery of triamcinolone acetonide to the suprachoroidal space. In October 2021, it was FDA-approved for the treatment of uveitic macular edema. The PEACHTREE trial, comprising 160 patients randomized to either CLS-TA or sham, was the pivotal phase 3 trial demonstrating that 47% of subjects in the CLS-TA arm gained 15 or more letters compared to 16% in the control group with a favorable mean reduction in central subfield thickness compared to the sham group (153 vs 18 microns) (P<0.0001). Elevated intraocular pressure was seen in 11.5% of the CLS-TA group compared to 15.6% in the control group.[4] The MAGNOLIA study evaluated the time to rescue over the 48-week period and revealed the median time to rescue was 257 days compared to 55.5 days in the CLS-TA compared to the control group, respectively.[5]
There are several drugs in development aimed at targeting the suprachoroidal space. Clinical trials involving the use of tyrosine kinase inhibitors (TKIs) in the treatment of AMD are ongoing.[6]
Gene therapy and treatments for choroidal melanoma are also being investigated.[7,8]
Yeh S, Khurana RN, Shah M, et al. Efficacy and Safety of Suprachoroidal CLS-TA for Macular Edema Secondary to Noninfectious Uveitis: Phase 3 Randomized Trial. Ophthalmology. 2020;127(7):948-955.
Khurana RN, Merrill P, Yeh S, et al. Extension study of the safety and efficacy of CLS-TA for treatment of macular oedema associated with non-infectious uveitis (MAGNOLIA) [published online ahead of print, 2021 Mar 12]. Br J Ophthalmol. 2021;bjophthalmol-2020-317560.
Avery R. Two Year Results from the Subretinal RGX-314 Gene Therapy Phase 1/2a Study for the Treatment of Neovascular AMD, and an Update on Suprachoroidal Trials. American Academy of Ophthalmology Subspecialty Day; 2021, 2021; New Orleans.
Klufas M. Suprachoroidal Delivery of RGX-314 for Diabetic Retinopathy Without CI-DME: Results from the Phase II ALTITUDE™ Study. Angiogenesis, Exudation and Degeneration; 2022, 2022; Virtual.
The administration of a drug into the suprachoroidal space varies from that of an intravitreal injection. To perform the injection:
Please see Video 34.2.1 for demonstration by Dr. James C. Major.
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Westmead Eye Manual
This invaluable open-source textbook for eye care professionals summarises the steps ophthalmologists need to perform when examining a patient.