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“Since last year we have made good progress on executing on our strategy to develop life-changing therapies for patients in need, through a diversified pipeline with a balanced risk profile,” said Daniel A. de Boer, CEO of ProQR. 2021-03-25 ProQR has programs in multiple therapeutic areas, such as cystic fibrosis and the rare skin condition Dystrophic epidermolysis bullosa, but ophthalmology assets make up the bulk of its pipeline. Pipeline Prospector delivers free access to a database of drugs under clinical trials which made headlines done by ProQR Therapeutics ProQR Therapeutics N.V is primarely in the business of pharmaceutical preparations. For financial reporting, their fiscal year ends on December 31st.

Proqr pipeline

About us; Vision 2023; Leadership; Careers; Contact; Science & Pipeline. Research and development pipeline; Clinical Trials. QR-1123 Aurora phase 1/2 study for adRP; Sepofarsen ILLUMINATE phase 2/3 study for LCA10; QR-421a STELLAR phase 1/2 study for Usher syndrome; Sepofarsen INSIGHT – phase 1b/2 study for LCA10; Sepofarsen ProQR Therapeutics N.V.Investor Contact: Sarah Kiely ProQR Therapeutics N.V. T: +1 617 599 6228 skiely@proqr.com or Hans Vitzthum LifeSci Advisors T: +1 617 535 7743 hans@lifesciadvisors.comMedia ProQR’s pipeline now includes two clinical programs, one preclinical program and two programs ready to enter development. “Since last year we have made good progress on executing on our strategy to develop life-changing therapies for patients in need, through a diversified pipeline with a balanced risk profile,” said Daniel A. de Boer, CEO of ProQR. LEIDEN, Netherlands, Nov. 30, 2015 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing lives through the creation of transformative RNA medicines for the treatment of severe orphan diseases such as cystic fibrosis (CF) and Leber's congenital amaurosis (LCA), today presents an update on the innovation pipeline and announces an R&D day for investors.

“We are pleased to see QR-421a advancing to pivotal testing and proud to support the work of ProQR as they advance their pipeline of RNA therapies to potentially help children, adults, and families who are affected by blindness caused by USH2A mutations and other rare inherited retinal diseases.” Phase 1/2 Stellar trial of QR-421a The Dutch biotech has firmed up its finances as its promising pipeline of RNA therapies for rare genetic eye disease starts to move through the clinic.

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ProQR Therapeutics NV is a biopharmaceutical company, which engages in the discovery and development of RNA therapies for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis pigmentosa. Its product pipeline include Sepofarsen, QR-421a, QR-1123, and QR-504a. The therapies in the ProQR pipeline utilize an RNA oligonucleotide technology platform to repair genetic defects, targeting significant parts of the mutations that are known causes of inherited ProQR Therapeutics is dedicated to changing lives through the creation of transformative RNA therapies for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10 LEIDEN, the Netherlands & CAMBRIDGE, Mass., Jan. 29, 2019 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (PRQR), a company dedicated to changing lives through the creation of transformative RNA About ProQR ProQR Therapeutics is dedicated to changing lives through the creation of transformative RNA therapies for the treatment of severe genetic rare diseases such as Leber congenital ProQR’s pipeline now includes two clinical programs, one preclinical program and two programs ready to enter development. “Since last year we have made good progress on executing on our strategy to develop life-changing therapies for patients in need, through a diversified pipeline with a balanced risk profile,” said Daniel A. de Boer, CEO of ProQR.

ProQR's Drug Candidate QRX-411 for Usher Syndrome

ProQR Therapeutics N.V. Investor Contact:Sarah KielyProQR Therapeutics N.V.T: +1 617 599 6228skiely@proqr.comorHans VitzthumLifeSci AdvisorsT: +1 617 430 2021-03-11 2020-09-14 2021-03-25 2021-04-20 2020-09-01 2019-05-17 2020-07-14 2017-06-15 2021-04-03 ProQR’s pipeline now includes two clinical programs, one preclinical program and two programs ready to enter development. “Since last year we have made good progress on executing on our strategy to develop life-changing therapies for patients in need, through a diversified pipeline with a balanced risk profile,” said Daniel A. de Boer, CEO of ProQR.

“We are pleased to see QR-421a advancing to pivotal testing and proud to support the work of ProQR as they advance their pipeline of RNA therapies to potentially help children, adults, and families who are affected by blindness caused by USH2A mutations and other rare inherited retinal diseases.” Phase 1/2 Stellar trial of QR-421a Upcoming Data and Focus. QR-313 is the short term catalyst amongst many that ProQR has in their pipeline. The company is expected to present Phase I/II interim data in the first quarter of 2019. With March newly here, the company is approaching the timeline that they set out. 2021-03-31 ProQR R&D day Highlights Progress on Pipeline and Introduces Axiomer®, a novel proprietary RNA Technology ProQR to host an R&D day in New York today, June … Learn more about ProQR at www.proqr.com.
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QRX-411 and QRX-421 are candidate molecules that will be presented in two 2019-05-17 · Wings Therapeutics has assumed control of ProQR’s pipeline dedicated to DEB and will take over the ongoing Phase 1/2 WINGS trial (NCT03605069) testing QR-313 for patients with recessive DEB due to mutations in exon 73 of the COL7A1 gene. Key program features and updates: ProQR to host an R&D day in New York today, June 15, from 8:00am to 1:00pm Eastern Standard Time. The live webcast can be accessed at | April 23, 2021 2021-04-20 · LEIDEN, Netherlands & CAMBRIDGE, Mass., April 20, 2021 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq: PRQR) (the “Company”), a company dedicated to changing lives through the creation of transformative RNA therapies for inherited retinal diseases (IRDs), today announced the Annual General Meeting of Shareholders will take place on Wednesday, May 19, 2021 at 16:00 CET (10:00am EDT Despite this, ProQR can still be a very interesting candidate to add to your watchlist. Hence, it is necessary to have a closer look at the company’s current situation, including its pipeline Company Overview. ProQR has a U.S. campus in Cambridge, Mass., but is headquartered out of The Netherlands.

At ProQR science is literally at the heart of what we do. The offices at our headquarters in Leiden are centered around the laboratories where our scientists discover and test our novel RNA therapies. ProQR’s pipeline now includes two clinical programs, one preclinical program and two programs ready to enter development. “Since last year we have made good progress on executing on our strategy to develop life-changing therapies for patients in need, through a diversified pipeline with a balanced risk profile,” said Daniel A. de Boer, CEO of ProQR. Learn more about our Pipeline of RNA therapies. Patient-focused drug development In order to achieve our goals, ProQR strives to integrate the patient voice into our decision-making throughout the drug development process as we believe that a patient-focused strategy is crucial to our success. PRQR boasts a pipeline of 18 drug candidates, nearly all in early-stage development.
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ProQR offers upbeat interim analysis in Phase 1/2 trial of QR-421a for Usher these data represent the second program from our ophthalmology pipeline that is Köp aktien ProQR Therapeutics N.V. - Ordinary Shares (PRQR). Hos Nordnet kan du handla från 0 kr i courtage. Klicka här för att följa aktiekursen i realtid. The STELLAR trial will explore whether QR-421a (ProQR's RNA therapy) we are growing our pipeline with patients and loved ones in mind. ProQR and the Cystic Fibrosis Foundation Therapeutics intend to expand we are growing our pipeline with patients and loved ones in mind.

ProQR Therapeutics - Striving to reverse blindness ProQR’s pipeline now includes two clinical programs, one preclinical program and two programs ready to enter development. We are ProQR, a biotechnology company dedicated to changing lives by developing RNA therapies for rare genetic diseases. We focus our drug development mainly on a group of blinding disorders affecting the retina, called inherited retinal diseases. We are on a mission “We are pleased to see QR-421a advancing to pivotal testing and proud to support the work of ProQR as they advance their pipeline of RNA therapies to potentially help children, adults, and families who are affected by blindness caused by USH2A mutations and other rare inherited retinal diseases.” Phase 1/2 Stellar trial of QR-421a Shares of ProQR Therapeutics (NASDAQ:PRQR) were trading higher on Wednesday after the company released positive results from a clinical trial for one of its leading pipeline candidates, QR-421a.
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ProQR Announces Positive Top-Line Results from a Phase 1b

The live webcast can be accessed at | February 28, 2021 2020-07-14 2017-06-15 2016-03-01 Summary. Ophthalmic RNA therapy concern ProQR Therapeutics N.V. (PRQR) has seen its share price more than half since its 2014 IPO. Promising Phase 1/2 data from its lead candidate (sepofarsen) has 2021-03-11 At ProQR we know first-hand what impact rare disease make to patients and their loved ones, and therefore we always put patients first. Our current pipeline includes treatments for Leber congenital amaurosis, Usher syndrome and retinitis pigmentosa. ProQR Therapeutics’s tracks 2020-09-01 2017-05-01 ProQR expanded its platform and pipeline with QR-110 for the treatment of Leber's Congenital Amaurosis (LCA), the leading genetic cause of blindness in childhood.

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About the Foundation Fighting Blindness Established in 1971, the Foundation Fighting Blindness is the world’s leading private funding source for retinal degenerative disease research. R&D pipeline RNA therapies for rare genetic diseases At ProQR we develop antisense oligonucleotides, or RNA therapies, to treat genetic diseases that are rare. We have made significant progress in advancing our broad pipeline of investigational medicines through the various stages of drug development, from early discovery to late stage clinical trials. Science & Pipeline RNA technology to benefit patients. RNA technology to benefit patients.