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Latest Market Reports

Market Scope's industry reports are meticulously prepared by a dedicated team of in-house consultants/analysts with over 100 years of collective experience.

Latest Industry News & Trends

5/9/2025
AIBreakingDealsDiagnosticOculomicsRetina
Topcon Healthcare Acquires RetInSight to Advance AI-Powered Imaging in Eye Care
Topcon Healthcare Acquires RetInSight to Advance AI-Powered Imaging in Eye Care

Topcon Healthcare announced May 2 that it had acquired privately held retinal AI analysis company RetInSight, of Austria. No financial details were disclosed. The companies forged a partnership in ...

5/9/2025
BiosimilarsBreakingCataractDry EyeIOLRefractiveRetinaRevenueSurgicalThyroid Eye Disease
Q1-2025 Ophthalmic Revenue Roundup for Amgen, Hoya, Apellis, Tarsus, STAAR, RxSight, and Ocular Therapeutix
Q1-2025 Ophthalmic Revenue Roundup for Amgen, Hoya, Apellis, Tarsus, STAAR, RxSight, and Ocular Therapeutix

​ Amgen, of Thousand Oaks, California, reported May 1 that its Q1-2025 revenue from Tepezza was $381 million, a 10 percent decrease from $424 million in Q1-2024. The total consisted of $365 million...

5/9/2025
BreakingDealsDry Eye
Elanco Sells US Royalty and Milestone Rights for Xdemvy to Blackstone for $295 Million
Elanco Sells US Royalty and Milestone Rights for Xdemvy to Blackstone for $295 Million

Elanco, of Greenfield, Indiana, announced May 5 that it had sold certain future US tiered royalties and commercial milestone payments associated with Tarsus’ Xdemvy (lotilaner ophthalmic solution 0...

5/9/2025
BreakingClinical TrialCorneal
Okyo Pharma Accelerates Development of Urcosimod in Neuropathic Corneal Pain
Okyo Pharma Accelerates Development of Urcosimod in Neuropathic Corneal Pain

London’s Okyo Pharma announced April 30 that it would accelerate development of urcosimod, formerly OK-101, in neuropathic corneal pain, following early closure of its Phase II trial. The trial was...

5/9/2025
BreakingDiagnosticFundusRegulationRetina
US FDA Grants Marketing Clearance for OcuSciences’ OcuMet Beacon Retinal Imager
US FDA Grants Marketing Clearance for OcuSciences’ OcuMet Beacon Retinal Imager

OcuSciences, of Ann Arbor, Michigan, announced May 1 that the US FDA had granted marketing clearance for its flagship device, the OcuMet Beacon retinal imager. The 510(k) clearance describes the Oc...

5/9/2025
AIBreakingDiagnosticEuropeFundusRegulationRetina
RetinAI and FVS Gain CE Marking for LuxIA DR Screening Algorithm
RetinAI and FVS Gain CE Marking for LuxIA DR Screening Algorithm

Switzerland’s RetinAI and Spain’s Fundación Ver Salud (FVS) announced April 30 that LuxIA, their co-developed artificial intelligence algorithm for diabetic retinopathy screening, had received CE m...

5/9/2025
BreakingClinical TrialDry EyeRegulation
Aldeyra Achieves Primary Endpoint in Phase III Dry Eye Chamber Trial of Reproxalap, Plans NDA Resubmission
Aldeyra Achieves Primary Endpoint in Phase III Dry Eye Chamber Trial of Reproxalap, Plans NDA Resubmission

Aldeyra Therapeutics reported May 5 that topical reproxalap achieved the primary endpoint of statistically significant improvement in ocular discomfort vs. vehicle in a Phase III dry eye chamber tr...

5/9/2025
BreakingGene TherapyRegulationRetina
US FDA Grants RMAT Status to Opus’ LCA5 Gene Therapy Candidate
US FDA Grants RMAT Status to Opus’ LCA5 Gene Therapy Candidate

Opus Genetics announced May 6 that the US FDA had granted regenerative medicine advanced therapy (RMAT) designation to OPGx-LCA5, its investigational gene therapy for the treatment of Leber congeni...

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