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Ledenoverzicht

PlayBall10

  • Lid sinds 22 okt 2004

    Laatste bezoek 15 jul 2024

Forumberichten

Frm. Topic / Post Postinfo
PRO

ProQR Announces Fourth Quarter and Full Year 2021 Operating and Financial ResultsAdditional analyses ongoing from Phase 2/3 Illuminate trial of sepofarsen in LCA10 with updates on any potential ne...

PRO

www.proqr.com/press-releases/proqr-an...ProQR Announces First Quarter 2021 Operating and Financial Results- Phase 2/3 pivotal Illum...

PRO

Nog een podcast, nu met de CEO: globalgenes.org/rare-cast/episode-309/ ...

PRO

ProQR Announces Virtual Presentation of Phase 1/2 Sepofarsen Data Through the Association for Research in Vision and Ophthalmology (ARVO)ir.proqr.com/news-releases/news-relea...

GAL

[quote alias=Mj25 id=12198526 date=202003101905]Mensen even een vraag, waar kan ik de openingskoersen van de aandelen n de indexen vinden? Ik heb me al suf gegoogeled en bij binck gekeken maar...

PRO

ProQR (PRQR) Receives a Buy from H.C. Wainwrightwww.smarteranalyst.com/brief/proqr-pr...

PRO

ProQR In-licenses Worldwide Rights to Ophthalmology Drug Candidate from Ionis Pharmaceuticalsir.proqr.com/news-releases/news-relea...

PRO

ProQr boekt vooruitgang met medicijn tegen zeldzame blindheidHet Nederlandse biotechbedrijf ProQr PRQR$12,55+57,86% heeft mogelijk een medicijn ontwikkeld tegen LCA10, een zeldzame ziekte die blindh...

PRO

First Human Trial to Evaluate QR-313 for Dystrophic Epidermolysis Bullosa Initiatedwww.raredr.com/news/first-human-trial...

PRO

ProQR Announces Presentations at ECFS on Eluforsen for F508del Cystic Fibrosis and at CFF Research Conference4 June 2018 at 7:00 AM EDTLEIDEN, The Netherlands, June 04, 2018 (GLOBE...

PRO

Daniel de Boer, Founder and CEO of ProQR, discusses Leber’s congenital amaurosis (LCA), the most common genetic cause of childhood blindness that affects about 15,000 patients in the Western world. ...

PRO

Aescap 2.0 passed 5% threshold in biotech ProQRYesterday evening Aescap 2.0 filed with the SEC that it has crossed the 5% shareholding threshold and currently owns 5.6% of the Nasdaq listed Dutch ...

PRO

Helaas. Het laatste wat ik van Leerink heb is van 14 februari....

PRO

ir.proqr.com/static-files/6a5fbdf0-1f...ProQRs Annual Magazine 2017We started ProQR Therapeutics five years ago to find a treatment for cystic fibrosis. Since...

PRO

Galapagos, Editas, Ionis und ProQR jagen Vertex im Kampf um den Milliardenmarkt Mukoviszidosewww.fool.de/2018/03/14/galapagos-edit...

PRO

labiotech.eu/proqr-cystic-fibrosis-da...

PRO

Mooie wetenschappelijke publicatie over Fuchs, een van de oog indicaties van ProQr ...

PRO

Nieuwe analist: Opus National Capital Markets.ProQR Therapeutics N.V. (PRQR): Leveraging its Expertise in mRNA Correction – Many Shots on Goal Given the Numerous Treatable Diseases: Initiating BUY/$...

PRO

30th Annual ROTH ConferenceOn Monday, March 12, 2018 at 12:00 pm PT, Smital Shah, Chief Financial Officer of ProQR, will present at the 30th Annual Roth Conference. The conference is being held at ...

PRO

Wainwright: ProQR Pivots in 2018 to Focus on Ophthalmology Opportunities. Rating: Buy; Price Target: $40.00...

PRO

JMP: In-Line Financials as PRQR Pushes Rare Disease Pipeline into the Clinic...

PRO

Leerink: 4Q Recap: All Eyes Set on Pompe/Fabry Updates in 2Q/3Q; PT to $22 / Outperform...

GAL

twitter.com/MorphoSys www.aad.org/scientificsessions/am2018...

PRO

Nogmaals Leerink...

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Nu in pdf (gisteren meerdere keren geprobeerd)...

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JMP...

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Leerink...

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labiotech.eu/galapagos-proqr-fibrosis...

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Leerink 8 januari 2018...

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www.biocentury.com/bc-extra/company-n...

PRO

ProQR and Galapagos Announce Research Collaboration on Fibrosis Targets Using ProQR’s Axiomer technology8 January 2018 at 7:00 AM ESTLEIDEN, the Netherlands, Jan. 08, 2018 (G...

PRO

ProQR Receives Orphan Drug Designation from EMA for Drug Candidate QR-313 for Dystrophic Epidermolysis Bullosa Key Updates•ProQR’s drug candidate, QR-313 for dystrophic epidermolysis bullo...

PRO

Leerink:• Bottom Line: Today PRQR announced dosing of the first patientin its ph.1/2 program for QR-110 in Leber’s congenital amaurosis10 (LCA 10), a rare genetic disorder resulting in blindness...

PRO

ProQR Doses First LCA 10 Patient in Clinical Trial of QR-110, ProQR’s Lead Program for Genetic Blindness Key Updates•The first patient has received the first dose of QR-110 in the Phase 1/...

PRO

ProQR Appoints Thaddeus Dryja, M.D. to Scientific Advisory Board Dr. Thaddeus (Ted) Dryja, a pioneer in the field of retinal genetic diseases, joins the Company’s Scientific Advisory Board.Dr. ...

PRO

cysticfibrosisnewstoday.com/2017/11/0...

PRO

JPG...

PRO

De analisten blijven positief. Wainwright....

GAL

Deel 4 en slot...

GAL

Onno van de Stolpe in Effect (VEB): Ik denk overigens dat we de komende jaren wat betreft organisatie en resultaat en dus beurswaarde zo snel kunnen groeien dat het lastiger wordt voor Gilead om te ov...

GAL

Deel 2...

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Deel 3...

PRO

ProQR to Present at the Chardan Inaugural Gene Therapy ConferenceLEIDEN, the Netherlands, Oct. 06, 2017 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing liv...

PRO

ProQR’s Inhaled RNA Therapy Improves CF Symptoms in Phase 1 Clinical Trialcysticfibrosisnewstoday.com/2017/09/2...

PRO

En tot slot Wainwright...

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Dank ivet voor het plaatsen van de rapporten. Hierbij de volledige versie van Leerink...

PRO

JMP...

PRO

JMP - koersdoel $14...

PRO

ProQR to Present at Two Investor Conferences in SeptemberLEIDEN, the Netherlands, Sept. 21, 2017 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR) today announced that the Company will prese...

PRO

ProQR Presents in vivo Proof of Concept Data for the Axiomer RNA Editing Platform TechnologyKey updatesProQR presents in vivo data in a relevant disease model, establishing proof of concep...