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European Regulators May Decline Approval for Apellis Pharmaceuticals’ Eye Disease Drug\n\nApellis Pharmaceuticals, a leading biopharmaceutical company, has received disappointing news from European regulators regarding its eye disease drug, Syfovre. The company has been informed that the European drug regulators advisory panel may decline to back an authorization for its drug to treat a chronic eye disease. This news has caused a significant drop in the company’s stock, with APLS tumbling below its 200-day line.\n\nThe drug in question, a form of pegcetacoplan directly injected in the back of the eye, was expected to receive approval for use in patients with geographic atrophy, an advanced form of a disease that leads to degeneration of a part of the eye called macula. The company has been informed that the panel may vote against the drug at the next meeting on January 22-25.\n\nThis news comes as a disappointment for Apellis Pharmaceuticals, as the company has been working towards providing a treatment option for the more than 2.5 million people in Europe affected by this disease. The rejection from the European regulators may have a significant impact on the company’s future plans and developments.\n\nIn a statement, Apellis Pharmaceuticals expressed its disappointment and stated that it will continue to work closely with the European regulators to address any concerns and provide additional data to support the approval of Syfovre. The company remains committed to finding a treatment option for the millions of people affected by this disease.\n\n Apellis Pharmaceuticals has received news that the European drug regulators advisory panel may decline to back an authorization for its eye disease drug, Syfovre. This has caused a significant drop in the company’s stock and may have a significant impact on its future plans.

” European Regulators May Decline Approval for Apellis Pharmaceuticals’ Eye Disease Drug\n\nApellis Pharmaceuticals, a leading biopharmaceutical company, has received disappointing news from European regulators regarding its eye disease drug, Syfovre. The company has been informed that the European drug regulators advisory panel may decline to back an authorization for its drug to treat a chronic eye disease. This news has caused a significant drop in the company’s stock, with APLS tumbling below its 200-day line.\n\nThe drug in question, a form of pegcetacoplan directly injected in the back of the eye, was expected to receive approval for use in patients with geographic atrophy, an advanced form of a disease that leads to degeneration of a part of the eye called macula. The company has been informed that the panel may vote against the drug at the next meeting on January 22-25.\n\nThis news comes as a disappointment for Apellis Pharmaceuticals, as the company has been working towards providing a treatment option for the more than 2.5 million people in Europe affected by this disease. The rejection from the European regulators may have a significant impact on the company’s future plans and developments.\n\nIn a statement, Apellis Pharmaceuticals expressed its disappointment and stated that it will continue to work closely with the European regulators to address any concerns and provide additional data to support the approval of Syfovre. The company remains committed to finding a treatment option for the millions of people affected by this disease.\n\n Apellis Pharmaceuticals has received news that the European drug regulators advisory panel may decline to back an authorization for its eye disease drug, Syfovre. This has caused a significant drop in the company’s stock and may have a significant impact on its future plans.”$APLS2023-12-18T17:40:37.899Z

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