OClawVPS.com
ProQR Therapeutics
Edit

ProQR Therapeutics

http://www.proqr.com/
Last activity: 26.05.2025
Active
Categories: ActiveBioTechDeliveryDevelopmentDrugIndustryLEDLivingPlatformTechnology
Dedicated to changing lives by developing novel RNA therapies for people living with severe genetic rare diseases that currently have no treatment options.
Likes
105
Followers
1.61K
Followers
6.05K
Mentions
13
Location: Netherlands, South Holland, Leiden
Employees: 51-200
Phone: +31 88 166 7000
Founded date: 2012

Investors 5

Mentions in press and media 13

DateTitleDescription
11.12.2024ProQR Therapeutics Announces $8.1 Million in New Funding from Rett Syndrome Research Trust to Expand RNA Editing CollaborationLEIDEN, Netherlands & CAMBRIDGE, Mass., Dec. 11, 2024 (GLOBE NEWSWIRE) -- ProQR Therapeutics NV. (Nasdaq: PRQR) (ProQR), a company dedicated to changing lives through transformative RNA therapies based on its proprietary Axiomer™ RNA ed...
13.03.2024ProQR Announces Year End 2023 Operating and Financial Results-
04.10.2022A top Wall Street analyst names 3 tiny biotechs that look like takeout targets — including one that could jump more than 1,000%The British pharma giant AstraZeneca has quietly been working on gene-editing research over the past few years. AstraZeneca This story is available exclusively to Insider subscribers. Become an Insider and start reading now. Redeem now Seve...
04.11.2021ProQR Announces Third Quarter 2021 Operating and Financial ResultsTop-line data from pivotal Phase 2/3 Illuminate trial of sepofarsen for CEP290-mediated LCA10 anticipated late Q1/early Q2 2022Five-target collaboration with Lilly highlights significant potential of ProQR’s Axiomer® RNA base-editing platfo...
17.06.2021PROQR THERAPEUTICS N.V. ProQR Therapeutics N : Plain-language summary of Retina Leroy BP, et al. paperThis plain-language summary (or PLS) describes a paper on Leber congenital amaurosis 10 that was published in a medical journal called "Retina". Title of the paper: Leber congenital amaurosis due to CEP290 mutations - severe visio...
06.05.2021PROQR THERAPEUTICS N.V. ProQR Announces First Quarter 2021 Operating and Financial ResultsPhase 2/3 pivotal Illuminate trial of sepofarsen for LCA10 enrollment complete with top-line data anticipated in H1 2022Positive data reported from the Phase 1/2 clinical trial of QR-421a for the treatment of Usher syndrome and non-syndromi...
24.03.2021ProQR’s RNA therapy on track to pivotal tests in rare, inherited form of vision lossNetherlands-based ProQR is developing its experimental therapy, QR-421a, as a treatment for Usher syndrome. The rare disorder is caused by mutations to genes that provide the instructions for proteins key to hearing, vision, and balance. Th...
31.03.2020My­ovant grabs $40M up­front in re­gion­al deal for re­l­u­golix; Akero an­nounces NASH suc­cess but Covid-19 de­lays→ Hav­ing just filed for the Eu­ro­pean ap­proval of its uter­ine fi­broids drug re­l­u­golix, My­ovant has sold the re­gion­al rights off to Hun­gar­i­an biotech Gedeon Richter. Com­pris­ing $40 mil­lion in up­front, $40 mil­lion in reg­u­...
14.12.2018Shinichi Tamu­ra re­claims the throne at So­sei; Jeff Abbey ex­its Ar­gos for No­vadip; Frank Cz­er­wiec is the new CMO at Goldfinch→ Jeff Abbey is jump­ing to the helm of Bel­gium’s No­vadip Bio­sciences af­ter lead­ing Ar­gos Ther­a­peu­tics as pres­i­dent and CEO for the past eight years. Hav­ing led No­vadip’s au­tol­o­gous cell ther­a­py through a Phase I/IIa tri­a...
13.09.2017ProQR spins out CNS assets to form RNA rare disease biotechProQR has spun out its CNS assets to form Amylon Therapeutics. The offshoot starts life with seed funding and an RNA-based program targeting a rare genetic disease that causes strokes. Amylon will further develop ProQR’s research into beta ...
Show more

Reviews 0

Sign up to leave a review

Sign up Log In