ProQR’s QRX-421 for Usher Syndrome receives ODD from FDA and EMA [Seeking Alpha]
ProQR Therapeutics N.V. - Ordinary Shares (PRQR)
Last proqr therapeutics n.v. - ordinary shares earnings: 2/26 07:00 am
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Source: Seeking Alpha
ProQR Therapeutics N.V. (NASDAQ: PRQR ) announces that investigational drug QRX-421 for Usher syndrome has received orphan drug designation (ODD) from the FDA and European Medicines Agency (EMA), representing the third drug candidate in the company’s ophthalmology pipeline and the fourth in the broader pipeline to receive ODD from the FDA and EMA. QR-421 is an investigational RNA-based oligonucleotide designed to address the underlying cause of Usher syndrome due to mutations in exon 13 of the USH2A gene. Usher syndrome is the leading cause of combined deafness and blindness. ODD in the U.S. and European Union provides a special status for investigational drugs being developed for rare diseases. The ODD programs offer development program tax benefits and a waiver of the NDA application user fee, as well as market exclusivity for up to seven years in the U.S. and ten years in the European Union following market approval. Now read: Progenics's Azedra: What's Wr
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News
- ProQR Nominates Martin Maier, PhD to Board and Announces Annual Meeting of Shareholders to be Held May 22, 2024GlobeNewswire
- ProQR Highlights Upcoming Presentations on Axiomer™ RNA Editing at ASGCT 27th Annual MeetingGlobeNewswire
- ProQR Achieves Successful Defense of New Challenge to its Axiomer™ IP Portfolio [Yahoo! Finance]Yahoo! Finance
- ProQR Achieves Successful Defense of New Challenge to its Axiomer™ IP PortfolioGlobeNewswire
- ProQR Therapeutics (NASDAQ: PRQR) had its price target raised by analysts at Citigroup Inc. from $1.80 to $2.00. They now have a "buy" rating on the stock.MarketBeat
PRQR
Earnings
- 11/7/23 - Miss
PRQR
Sec Filings
- 4/23/24 - Form 6-K
- 4/19/24 - Form 6-K
- 3/13/24 - Form 20-F
- PRQR's page on the SEC website