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Neurotech’s ENCELTO has marked a historic milestone by becoming the first and only FDA-approved treatment for Macular Telangiectasia type 2 (MacTel), a rare and progressive retinal disease. This achievement brings new hope to individuals suffering from MacTel, offering them a chance to preserve their vision and improve quality of life.
MacTel is a degenerative condition affecting the central part of the retina, which leads to severe vision impairment. Until recently, there were no FDA-approved treatments available for this disease. Now, with the approval of Neurotech’s ENCELTO, patients have access to the first ever effective therapy.
Neurotech’s ENCELTO employs a novel approach called encapsulated cell technology, which delivers continuous, localized doses of ciliary neurotrophic factor (CNTF) to the retina. This approach helps slow the progression of retinal degeneration and preserves vision in patients with MacTel.
The implant is a one-time surgical procedure that releases CNTF steadily over several years, providing sustained therapeutic benefits without the need for frequent injections. Clinical trials have shown that this therapy significantly preserves retinal structure and visual function, offering patients improved sight and a better quality of life.
The ENCELTO FDA approval by the U.S. Food and Drug Administration marks a major breakthrough in the treatment of MacTel. The therapy has been proven to slow the progression of the disease and preserve central vision for patients, providing them with a rare opportunity to manage the disease effectively.
This approval is not just a triumph for patients, but also a testament to Neurotech’s commitment to advancing innovative treatments for retinal diseases. The success of ENCELTO has also opened the door for further research into other diseases of the retina, such as age-related macular degeneration and diabetic retinopathy.
For patients diagnosed with MacTel, the approval of Neurotech MacTel therapy is life-changing. Clinical trials demonstrated that ENCELTO can effectively slow down disease progression, maintaining central vision and offering hope for a longer period of preserved vision. The therapy allows patients to maintain greater independence and continue with everyday activities.
The success of Neurotech’s ENCELTO offers new optimism for individuals with MacTel and sets a new standard in retinal disease treatment. The approval of this innovative therapy is just the beginning, with potential applications in other retinal diseases. With continued research and development, ENCELTO may pave the way for future breakthroughs in the treatment of degenerative eye conditions.
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Neurotech’s ENCELTO has marked a historic milestone by becoming the first and only FDA-approved treatment for Macular Telangiectasia type 2 (MacTel), a rare and progressive retinal disease. This achievement brings new hope to individuals suffering from MacTel, offering them a chance to preserve their vision and improve quality of life.
MacTel is a degenerative condition affecting the central part of the retina, which leads to severe vision impairment. Until recently, there were no FDA-approved treatments available for this disease. Now, with the approval of Neurotech’s ENCELTO, patients have access to the first ever effective therapy.
Neurotech’s ENCELTO employs a novel approach called encapsulated cell technology, which delivers continuous, localized doses of ciliary neurotrophic factor (CNTF) to the retina. This approach helps slow the progression of retinal degeneration and preserves vision in patients with MacTel.
The implant is a one-time surgical procedure that releases CNTF steadily over several years, providing sustained therapeutic benefits without the need for frequent injections. Clinical trials have shown that this therapy significantly preserves retinal structure and visual function, offering patients improved sight and a better quality of life.
The ENCELTO FDA approval by the U.S. Food and Drug Administration marks a major breakthrough in the treatment of MacTel. The therapy has been proven to slow the progression of the disease and preserve central vision for patients, providing them with a rare opportunity to manage the disease effectively.
This approval is not just a triumph for patients, but also a testament to Neurotech’s commitment to advancing innovative treatments for retinal diseases. The success of ENCELTO has also opened the door for further research into other diseases of the retina, such as age-related macular degeneration and diabetic retinopathy.
For patients diagnosed with MacTel, the approval of Neurotech MacTel therapy is life-changing. Clinical trials demonstrated that ENCELTO can effectively slow down disease progression, maintaining central vision and offering hope for a longer period of preserved vision. The therapy allows patients to maintain greater independence and continue with everyday activities.
The success of Neurotech’s ENCELTO offers new optimism for individuals with MacTel and sets a new standard in retinal disease treatment. The approval of this innovative therapy is just the beginning, with potential applications in other retinal diseases. With continued research and development, ENCELTO may pave the way for future breakthroughs in the treatment of degenerative eye conditions.
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