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Uveitis News

3/21/2025
BreakingDealsRegulationRetinaUveitis
US FDA Expands Label for Iluvien to Include Chronic Non-infectious Posterior Uveitis
US FDA Expands Label for Iluvien to Include Chronic Non-infectious Posterior Uveitis

ANI Pharmaceuticals, of Baudette, Minnesota, announced March 14 that the US FDA had approved an expanded label for Iluvien (fluocinolone acetonide intravitreal implant 0.19 mg) to include treatment...

3/20/2025
BiosimilarsChinaDry EyeGene TherapyIndustryNewsletterRefractiveRegulationRetinaUveitis
March 2025 Ophthalmic News Briefs
March 2025 Ophthalmic News Briefs

Alcon announced the US launch Feb. 24 of its Systane Pro Preservative-Free (PF) over-the-counter eye drops for dry eye. The company said Systane Pro PF is the longest lasting eye drop in the Systan...

2/28/2025
BreakingChinaRegulationRetinaUveitis
Chinese Regulators Accept NDA for Arcatus (Xipere) in Uveitic Macular Edema
Chinese Regulators Accept NDA for Arcatus (Xipere) in Uveitic Macular Edema

Clearside Biomedical announced Feb. 20 that Chinese regulators had accepted for review the new drug application (NDA) filed by Clearside’s Asia-Pacific partner, Arctic Vision, for Arcatus, known as...

2/20/2025
ChinaClinical TrialCornealDealsDry EyeGlaucomaIOLIndustryMyopiaNewsletterRegulationRetinaSurgicalUveitis
February 2025 Ophthalmic News Briefs
February 2025 Ophthalmic News Briefs

Outlook Therapeutics reported Jan. 16 the final results of the NORSE EIGHT trial of ONS-5010 (Lytenava), an ophthalmic formulation of bevacizumab for wet AMD. ONS-5010 demonstrated non-inferiority ...

1/24/2025
BreakingPharmaRegulationUveitis
Arctic Vision Gains Approval of Arcatus (Xipere) for Uveitic Macular Edema in Australia, Singapore
Arctic Vision Gains Approval of Arcatus (Xipere) for Uveitic Macular Edema in Australia, Singapore

Clearside Biomedical announced Jan. 22 that its Asia-Pacific partner, Arctic Vision, had gained approval in Australia and Singapore for Arcatus, known as Xipere in the US, for uveitic macular edema...

1/21/2025
AIBiosimilarsChinaClinical TrialCornealDiagnosticDry EyeEuropeIndustryNewsletterRefractiveRegulationRetinaStudyUveitis
January 2025 Ophthalmic News Briefs
January 2025 Ophthalmic News Briefs

China’s Eyebright Medical announced Jan. 7 that its phakic intraocular lens, the Loong Crystal PR, had received certification as a Class III medical device from the country’s National Medical Produ...

12/20/2024
BreakingClinical TrialRetinaUveitis
Acelyrin’s Izokibep Misses Endpoints in Phase IIb/III Uveitis Trial
Acelyrin’s Izokibep Misses Endpoints in Phase IIb/III Uveitis Trial

Acelyrin reported Dec. 10 that izokibep, an inhibitor of interleukin-17A, missed its endpoints in a Phase IIb/III trial in non-infectious, non-anterior uveitis. The company said it would drop izoki...

10/4/2024
BreakingRegulationRetinaUveitis
US FDA Grants Fast Track Designation to Priovant’s Uveitis Candidate
US FDA Grants Fast Track Designation to Priovant’s Uveitis Candidate

Priovant Therapeutics, of Durham, North Carolina, reported Sept. 23 that the US FDA had granted fast track designation for brepocitinib in non-infectious intermediate or posterior uveitis or panuve...

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