Polyneuron is proud to announce that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation to PN‑1007 (PPSGG) in the treatment of anti-MAG neuropathy, a disabling, chronic disorder of the peripheral nervous system. Orphan designation is granted to advance the development of safe and effective therapies for the treatment of rare diseases. The FDA may provide grant funding toward clinical trial costs, tax credits, FDA user-fee benefits, and seven years of market exclusivity following marketing approval.
In other news
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General
Polyneuron and University of Basel awarded grant of CHF 1.2 M to advance novel treatments to support ABO-Incompatible transplantsPolyneuron is proud to announce that – together with the… [read on]
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Uncategorized
Polyneuron appoints Aled Williams as chief business officerWe are extremely pleased to welcome Aled Williams to Polyneuron… [read on]
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General
Polyneuron extends Series A to CHF 36.5 millionPolyneuron announces a CHF 14 million extension of the Series… [read on]
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General
Polyneuron receives approval to begin clinical study with PN-1007 in anti-MAG neuropathyWe are very proud to have received our… [read on]
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General
Polyneuron announces appointment of chief medical officerWe are extremely pleased to welcome Dr Debra Barker to… [read on]
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General
Polyneuron annouces appointment of new ChairmanPolyneuron announces the appointment of Ben Machielse as Chairman of… [read on]
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Financing
Polyneuron raises CHF 22.5 million in a major Series A financingPolyneuron raises CHF 22.5 million in an oversubscribed… [read on]
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Financing
Completion of financing and team strengtheningPolyneuron announces the completion of a… [read on]