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Follow on Google News | Mobius Therapeutics™ Receives Final FDA Approval for New Glaucoma DrugFDA Approves Mitosol® for Immediate Production and Use in Glaucoma Surgery
“The approval of Mitosol® for use in glaucoma surgery represents the culmination of more than five years of work on the part of Mobius Therapeutics™ Glaucoma is the second-leading cause of blindness in the United States. It is treated progressively, beginning with pharmaceuticals, then office intervention and finally surgery. Mitosol® "The approval of Mitosol® is an important event on multiple levels", stated Dr. Henry D. Jampel, Odd Fellows and Rebekahs Professor of Ophthalmology at the Wilmer Eye Institute of Johns Hopkins University. "Surgeons, patients and operating room staff will benefit from improved precision, convenience, quality assurance, and safety." Mobius™ manufactures Mitosol® locally, using St. Louis-based sterile packaging, precision medical molding, commercial sterilization and pharmaceutical logistic firms. “We believe that Mobius represents a new and efficient model for merging a company’s strengths with the locally available resources,” said St. Louis Mayor Francis Slay. ”As part of the local life science community, Mobius’ approval represents a win not only for the company, but for the St. Louis economy as a whole.” About Mobius Therapeutics, LLC: Mobius Therapeutics is an early stage venture focused on ophthalmic surgery solutions. Its first product, Mitosol®, is a system for delivering antifibrotic agents in glaucoma, refractive, and corneal surgery. The glaucoma indication is in active commercialization; End
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