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ProQR to Participate in the Cantor Virtual Rare Orphan Disease Summit

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ProQR Therapeutics N.V. (Nasdaq: PRQR) announced participation in the Cantor Virtual Rare Orphan Disease Summit on March 29, 2022, from 2:45-3:45 PM EDT. The Company focuses on developing transformative RNA therapies for genetic eye diseases, including Leber congenital amaurosis 10 and Usher syndrome. ProQR uses proprietary RNA repair technologies to grow its pipeline, prioritizing patients' needs. For more information, visit www.proqr.com.

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LEIDEN, Netherlands & CAMBRIDGE, Mass., March 23, 2022 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq: PRQR) (the “Company”), a company dedicated to changing lives through the creation of transformative RNA therapies for genetic eye diseases, today announced that Company management will participate in the Cantor Virtual Rare Orphan Disease Summit on March 29 as part of the RNA Therapeutics in Rare Diseases panel from 2:45-3:45pm EDT.

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 amaurosis 10, Usher syndrome and retinitis pigmentosa. Based on our unique proprietary RNA repair platform technologies we are growing our pipeline with patients and loved ones in mind.

Learn more about ProQR at www.proqr.com.

FORWARD-LOOKING STATEMENTS

This press release contains forward-looking statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as "anticipate," "believe," "could," "estimate," "expect," "goal," "intend," "look forward to", "may," "plan," "potential," "predict," "project," "should," "will," "would" and similar expressions. Such forward-looking statements include, but are not limited to, statements regarding our participation in this conference. Forward-looking statements are based on management's beliefs and assumptions and on information available to management only as of the date of this press release. Our actual results could differ materially from those anticipated in these forward-looking statements for many reasons, including, without limitation, the risks, uncertainties and other factors in our filings made with the Securities and Exchange Commission, including certain sections of our annual report filed on Form 20-F. Given these risks, uncertainties and other factors, you should not place undue reliance on these forward-looking statements, and we assume no obligation to update these forward-looking statements, even if new information becomes available in the future, except as required by law.

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: +1 617 430 7578
hans@lifesciadvisors.com

Media Contact:
Robert Stanislaro
FTI Consulting
T: +1 212 850 5657
robert.stanislaro@fticonsulting.com


FAQ

When is ProQR Therapeutics participating in the Cantor Virtual Rare Orphan Disease Summit?

ProQR Therapeutics will participate on March 29, 2022, from 2:45-3:45 PM EDT.

What is the focus of ProQR Therapeutics at the summit?

ProQR Therapeutics will be part of the 'RNA Therapeutics in Rare Diseases' panel.

What genetic conditions does ProQR Therapeutics address?

ProQR Therapeutics focuses on severe genetic eye diseases such as Leber congenital amaurosis 10 and Usher syndrome.

What is the stock symbol for ProQR Therapeutics?

The stock symbol for ProQR Therapeutics is PRQR.

Where can I find more information about ProQR Therapeutics?

More information can be found at www.proqr.com.

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