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      Ophthalmologists estimate 10% of Geographic Atrophy patients are now treated with Syfovre since its February 2023 approval (MARKETVUE® REPORT)

      (PRNewsfoto/REACH Market Research)

      News provided by

      REACH Market Research

      Aug 17, 2023, 10:37 ET

      Share this article

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      Apellis's anti-C3 Syfovre (pegcetacoplan intravitreal injection) and Astellas' anti-C5 Izervay (avacincaptad pegol intravitreal injection) were both recently FDA-approved to treat Geographic Atrophy (GA), but physicians are eager for more treatment options, according to findings from REACH Market Research.

      NEWTON, Mass., Aug. 17, 2023 /PRNewswire/ -- Prior to the approvals of Syfovre and Izervay, the treatment for GA consisted of nonspecific therapies that do not target GA pathophysiology directly (e.g., dietary supplements and surgeries).

      Despite the availability of Syfovre for GA and significant number of patients receiving the drug already, interviewed ophthalmologists feel the functional benefit and safety profile of the drug could be improved.

      Ophthalmologist, U.S.: "With Syfovre, the vision's not getting better. In fact, the trials show it gets worse, not because of the drug but because of the natural history of the disease. Unfortunately, you can't measure improvement on visual acuity but if you did microperimetry you would see that you're maintaining these patients' vision, but not improving." 

      To access REACH's MarketVue® Report on Geographic Atrophy, visit https://reachmr.com or contact us at [email protected].  

      When asked about what improvements they'd like to see over Syfovre and Izervay, ophthalmologists report they would like to see less frequently administered products with fewer adverse events and treatments able to demonstrate improved functional benefit.

      Fortunately for GA patients, the pipeline is full of novel incoming treatment options in development. Ongoing phase 3 trials include:

      • Alkeus' oral chemically modified Vitamin A – ALK-001
      • Belite's oralanti-RBP4– LBS-008

      Bayley Koopman, Research Associate at REACH: "While approximately once monthly intravitreal injections represent the current standard of care, orally administered or 'one-and-done' treatments such as cell and gene therapies are in development for GA and could potentially reduce the burden of treatment if these therapies are able to demonstrate efficacy."

      About MarketVue®  

      MarketVue® reports are a rare disease focused, fresh alternative to traditionally long and outdated market research reports. MarketVue® reports cover rare disease epidemiology and key market dynamics based on research from key opinion leader interviews, physician surveys, and secondary data.  

      About REACH Market Research 

      REACH is an independent pharmaceutical market research company focused on rare and niche diseases. With decades of experience in pharmaceutical market research and life sciences consulting, REACH fills an important gap in the market – accessible market research solutions for rare and niche diseases.  

      SOURCE REACH Market Research

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