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ThromboGenics Business Update

Commercializing JETREA ® (ocriplasmin)   in the US

  • JETREA ® launched in the US on 14 January as the first pharmacological treatment for symptomatic vitreomacular adhesion (VMA)
  • Highly focused commercial team, including specialty sales force, now working to drive the US sales of JETREA ®
  • In absence of J-code, reimbursement specialists educate physicians on ThromboGenics' comprehensive reimbursement support program to assist US physicians in gaining reimbursement for JETREA ® and explaining relevant patient assistance programs
  • Code (reimbursement code) should be in place from 1 January 2014  - J-code will automate 'bill and payment' process for practices

Positive reaction to JETREA ® from US retina community:

  • Sales of $10.2 million since the product's US launch through the end of April
  • 40% of total targeted retina practices have ordered JETREA ®
  • 50% of these practices have reordered the product

Commercializing JETREA ® in Europe and ROW

  • In March 2013, the European Medicines Agency (EMA) approved JETREA ® for the treatment of vitreomacular traction (VMT), including when associated with macular hole of diameter less than or equal to 400 microns
  • The EU approval led to ThromboGenics receiving a €45 million milestone payment from Alcon
  • Thrombogenics received a further €45 million payment from Alcon in April 2013 for the first order of JETREA ® in Europe

JETREA ® Phase IIa wet AMD trial reporting:

  • ThromboGenics today reports positive data from a Phase IIa study showing that JETREA ® has potential to resolve VMA in patients with wet age-related macular degeneration (wAMD)
  • In the study, at Day 28 (primary endpoint, p=0.26), 24% of the treated patients achieved resolution compared to 12% in the sham injection arm
  • No unexpected safety issues were identified, and the safety profile is in keeping with the previous pivotal trial data
  • To confirm these clinical results, further larger studies to confirm clinical benefits are warranted

Financial Update

  • At the end of April 2013, the Company had a cash balance exceeding €200 million
  • In March, the Company's shares started trading as part of the BEL20 index on the Euronext stock exchange.

Dr  Patrik De Haes, CEO of ThromboGenics, said: " The start of 2013 has been a very positive period for ThromboGenics with our lead product JETREA ®   being launched in the  US  and  Europe . As a result, patients and physicians on both sides of the  Atlantic  now have access to the first pharmacological treatment for symptomatic VMA/VMT, an important sight-threatening condition. We are pleased with the positive reaction to JETREA ®   from the US retina community, and are confident that this momentum will continue.

"The EU approval of JETREA ®   and its recent launch in the UK and Germany triggered a total of €90 million in milestone payments from Alcon. These funds strengthen our financial position, and will allow us to invest further in the US commercialization of JETREA ® , develop new indications for this novel medicine and expand our R&D pipeline. Over the next 12 months we expect to generate further shareholder value as the US sales of JETREA ®   continue to build and we receive royalties from Alcon as JETREA ®   continues to be rolled out across Europe."  

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