Onno van de Stolpe

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Onno van de Stolpegrocery gateway promo code july 2020

And really want to start with thanking my organization for adapting very, very well to this exceptional situation. Thank you for the question. From 1998 to 1999, he was the Managing Director of Genomics at IntroGene B.V. (later Crucell N.V., which was acquired by Johnson & Johnson Services, Inc. in 2011). These forward-looking statements include remarks concerning future developments of the pipeline and our company, possible changes in the industry and the competitive environment. So those will add the power. If they have been dedicated or at least have major COVID-19 activities then clearly, they cannot recruit IPF patients for a trial. I think that will be an inspiration for others to come.”I definitely think that, with Galapagos, argenx and Genmab, we finally have three major biotech companies in Europe. Thanks, Walid. Thanks, Emily. And although at a slower pace, we are happy that we are -- we actually have now 1,000 -- over 1,000 patients recruited in that trial. That is Yes, and I’m a strong believer in harboring that innovation in biotech. Please reach out to the IR team, Sofie Van Gijsel or myself, if you have any questions. We have invested massively in research over the past couple of years and the project is now ready to move into the clinic (we’ll start our first Phase II studies this year).If Toledo is successful (and we’re all convinced that it will be), it will work even better than current drugs like the JAK inhibitors or the TNFs. Van de Stolpe Onno. And if so, sort of what some of the provisions would be in the case of sort of any missing data that could happen as a result of COVID in that trial?Yes. The pressure is on for the management teams to generate revenues, and not necessarily to embark on a 15-year path of development.As a CEO, you should have a dream. Yes. Or alternatively, are you just needing to upsize the trial, maybe a larger sample for the futility? That, of course, will be delayed also with regard to COVID-19.

Yes. And that 70% information is "derived" from those 33% of the patients who have been enrolled and have gone all the way through 52 weeks plus all of those behind them that are contributing to the various earlier endpoints, 9 months, 6 months and 3 months, to collectively help us estimate what the 1-year rate of decline in FVC would look like. And of course, now we're living in unusual circumstances, so I think we need to keep an eye out for this. And 1690 is now called ziritaxestat, which is the generic name of this drug that has been approved. So where we have plans that when we're in the clinic, we will brief the whole field broadly on the discovery, the identity and the promise we see in this program. Onno van de Stolpe founded Galapagos in 1999 and has served as Chief Executive Officer and a member of the board of directors from 1999 to the present.

That would be for all the MANTA program, both MANTA in the UC population as well as the MANTA in the rheumatology MANTA-RAy.

It's actually the number one cause for death in autoimmune diseases actually. I can’t think of a single good example where a biotech was bought by a pharma company and continued innovating as it did before. We'll come back to his question when we get Walid reconnected.You can't do 2 things at once. He received an MSc degree from Wageningen University. But the other centers can continue to recruit. Will it get worse? So just to get your thoughts on your expectations heading into the data would be great.Yes. And that's why we anticipate there's going to be a bit of a delay. And we thank everybody for the participation today. So this is -- we took -- essentially, this is a trial looking at scleroderma as a disease itself, not scleroderma with interstitial lung disease. And his take on this, and here I'm quoting, is to say, so far, in a large global database of IPF patients from the ISABELA program, we have seen a low event rate of possible COVID cases and no fatalities related to this at this point. So 1205, the PINTA study is a proof-of-concept in about 60 patients and what is new compared to FLORA is that here, patients are on what you call standard of care, which is then 1/3 of the patient is on nintedanib, 1/3 is on pirfenidone and 1/3 is on a local standard of care where none of these drugs is approved.

People start to invest more in local companies and Belgian students choose to study life sciences; it’s all part of the ecosystem. We always exclude some nonoperating items such as cash proceeds from warrant exercises or -- and translation effects on currency, as you see here on the slide. We'll take our first question from Christopher Marai with Nomura.First one is really on Toledo. They continue to come into the office and into the labs.

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