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Friday, March 19, 2010

Galapagos to build cystic fibrosis drug pipeline

Galapagos to build cystic fibrosis drug pipeline

Click here to access the live audio webcast R&D Update presentation today at 13.00 CET/8 AM EST, call number +32 2290 1791

Mechelen, Belgium; 19 March 2010 – Galapagos NV (Euronext: GLPG) announced the decision to pursue cystic fibrosis (CF) in its strategy to deliver breakthrough medicines to patients with orphan diseases. Details of Galapagos’ CF program and its pipeline of 4 clinical and over 50 pre-clinical and discovery programs will be discussed during the R&D Update presentation webcast later today.

Over the past years, Galapagos has established a strong franchise in orphan diseases. Galapagos has applied its proprietary target discovery platform in collaborations with the CHDI (for Huntington’s disease), the Cystic Fibrosis Foundation and the ALS Foundation. In addition, Galapagos is evaluating its SARM candidate drug, GLPG0492, for the treatment of Duchenne muscular dystrophy.

“Orphan diseases represent significant unmet clinical needs. The lack of novel disease-modifying therapies for these diseases presents significant opportunities for a company capable of delivering new mode-of-action therapies. Galapagos has made a strategic decision to pursue cystic fibrosis as the first orphan disease in which we will discover, develop and launch our own medicines. This decision is based on our successful collaboration with the CF Foundation, through which we have identified the first ever disease-modifying targets for CF,” said Onno van de Stolpe, CEO of Galapagos. “With this strategy, Galapagos expects to benefit from the accelerated approval procedures and exclusive commercial rights granted to developers of orphan drugs through US and European regulatory agencies, to ultimately provide real medical benefit to this sizeable population of patients.”

The CF Foundation and Galapagos entered a target discovery collaboration in 2005, which resulted in 19 novel disease-modifying targets that have been validated in the standard pre-clinical model for this disease. Galapagos has secured all rights to these targets and has started to develop small molecule therapies against a select group of these targets. Galapagos will retain intellectual property and commercial rights on any compounds reaching the market. Galapagos medicines in CF will be disease-modifying agents with clear efficacy benefits relative to existing therapies, which only treat the symptoms of the disease. A first pre-clinical candidate is scheduled to be nominated by 2013.

“We are confident that the strategic decision to enter CF drug discovery will provide new treatment options for CF patients and thus create long term value for our shareholders. In the first years, research expenses for this new strategy will be limited and we anticipate that the clinical trials to support approval can be financed by our strengthening cashflow,” said Van de Stolpe.

Conference call and webcast presentationGalapagos will conduct a conference call open to the public today at 13.00 Central European Time (CET), which will also be webcast. To participate in the conference call, please call +32 2290 1791 ten minutes prior to commencement. A question and answer session will follow the presentation of the results. Click here to access the live audio webcast. The archived webcast also will be available for replay shortly after the close of the call.About cystic fibrosisCystic fibrosis (CF) is a hereditary disease of the entire body which leads to severe disability and early death in many cases. Symptoms include frequent lung infections, sinus infections, poor growth, and diarrhea. The cause is a defect in gene which encodes for cystic fibrosis transmembrane conductance regulator (CFTR), a protein which regulates components of sweat, mucus, and digestive juices. CF affects approximately 70,000 people worldwide. Patient symptoms are treated with antibiotics and other medicines, with the global market expected to double from just over $1 billion in 2010 to $2 billion by 2015. There currently is no cure for the disease, and most patients die in their 30s due to lung failure. More info at: www.cff.org/AboutCF

About Galapagos Galapagos (Euronext: GLPG; OTC: GLPYY) is a mid-size biotechnology company specialized in the discovery and development of small molecule and antibody therapies with novel modes-of-action. The Company is progressing one of the largest pipelines in biotech, with four clinical and over 50 small molecule discovery/pre-clinical programs. Through risk/reward-sharing alliances with GlaxoSmithKline, Lilly, Janssen Pharmaceutica, Merck & Co. and Roche, Galapagos is eligible to receive up to €3 billion in downstream milestones, plus royalties. With the acquisition of Argenta, Galapagos now has more than 670 employees and operates facilities in six countries, with global headquarters in Mechelen, Belgium. More info at: www.glpg.com


Galapagos NVOnno van de Stolpe, CEOTel: +31 6 2909 8028
Elizabeth Goodwin, Director Investor RelationsTel: +31 6 2291 6240ir@glpg.com

1 comment:

  1. Hi! I found your blog through the CF Forum, and I'm particularly interested in your travel tips.

    We'll be going to Europe for three months this summer, and we need a compressor that will work over there for my one-year-old daughter with CF. We're planning to get a Pari Trek as a temporary fix, but I've heard that it's slower than the Pari ProNeb Ultra II and that it runs out of steam after a while. I've also heard that it isn't approved for use with Pulmozyme.

    Anyway, I'm wondering where you managed to buy a ProNeb Ultra II that works in Europe. If you would be willing to let me know and give me some tips for doing the same, that would be awesome! My e-mail is sarah.peris@yahoo.com.

    Thanks so much!