- Company announces departure of
Noreen R. Henig, Chief Medical Officer, promotion of Peter Adamsonto Senior Vice President Ophthalmology Franchise and Robert Friesento Senior Vice President Science and Early Development. David M. Rodman, M.D., Chief Development Strategy Officer will assume leadership of clinical development at the Company.
“In four years, ProQR has grown from a small company with big ideas to a RNA therapeutics company with two completed and positive clinical trials, a robust pipeline, and an incredibly talented team. I am truly proud of our achievements to date and believe the Company is positioned for continued growth,” said
“During her four-year tenure, Noreen was instrumental in the successful completion of two global clinical trials for QR-010 for CF patients, bringing QR-110 for LCA10 patients into the clinic and advancing QR-313 towards clinical development. On behalf of all ProQRians, I thank Noreen for her dedication and leadership and wish her the very best in her future endeavors,” said
In his promotion to SVP Ophthalmology Franchise,
“As we continue to build our pipeline, the promotion of Pete and Robert further enforce our senior leadership team,” said
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. 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. These forward-looking statements include, but are not limited to, statements regarding QR-010, QR-110 and QR-313, including the clinical development and therapeutic potential of each, future development plans and future performance of our executive team. Our actual results could differ materially from those anticipated in these forward-looking statements for many reasons, including, without limitation, risks associated with our clinical development activities, including that positive results observed in our prior and ongoing studies may not be replicated in later trials or guarantee approval of any product candidate by regulatory authorities, that a Fast Track designation by the
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Source: ProQR Therapeutics N.V.