Galapagos NV
Industriepark Mechelen Noord I, Zone L
Generaal De Wittelaan 11 A
Mechelen
B-2800
Tel: 32-15-34-29-00
Fax: 32-15-34-29-01
Website: http://www.galapagosgenomics.com/
562 articles with Galapagos NV
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Galapagos announces completion of patient enrollment for DIVERSITY Phase 3 study with filgotinib in Crohn’s Disease
10/4/2021
Galapagos NV announced randomization of the last patient into the multi-center, globalDIVERSITY Phase 3 study.
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Galapagos increases share capital through subscription right exercises - Sep 20, 2021
9/20/2021
Galapagos issued 7,600 new ordinary shares on 20 September 2021, for a total capital increase of €151,787.50.
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GALAPAGOS ANNOUNCES POSITIVE CHMP OPINION FOR JYSELECA® (FILGOTINIB) FOR THE TREATMENT OF ADULTS WITH MODERATELY TO SEVERELY ACTIVE ULCERATIVE COLITIS
9/17/2021
Galapagos NV today that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion for Jyseleca
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As CEO, Stolpe has presided over some highs with the launch of JAK1 inhibitor Jyseleca (filgotinib) in Europe, as well as the devaluation of the company's share price by 70%.
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Galapagos reports positive topline results with selective TYK2 inhibitor GLPG3667 in Phase 1b psoriasis study
7/14/2021
Galapagos NV (Euronext & Nasdaq: GLPG)reports positive topline resultswith tyrosine kinase 2 (TYK2) inhibitor GLPG3667 in a Phase 1b studyin psoriasis patients.GLPG3667 was discovered by Galapagos.
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Galapagos demonstrates early clinical activity with SIK2/3 inhibition in inflammation
7/14/2021
Galapagos NV(Euronext & Nasdaq: GLPG)reports topline results with GLPG3970 in three patientstudies.GLPG3970, the first product candidatefrom a broad portfolio of SIK inhibitor compounds, provides clinicaldatasupporting the role of SIK inhibition in inflammation.
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In its 2Q2021 Clinical Report, BioSpace highlights drugs that were greenlit for clinical studies, faced clinical and regulatory hurdles and some who saw regulatory wins.
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While the drug showed significant improvement in patients on a 200mg daily dose of filgotinib, it may not be promoted in the states any time soon.
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Galapagos announces new data supporting rapid symptom improvement and sustained steroid-free remission with filgotinib in patients with Ulcerative Colitis
7/10/2021
Mechelen, Belgium; 10 July 2021, 11.10 CET; Galapagos NV announced new post-hoc analyses from the Phase 3 SELECTION program, supporting the activity and tolerability of filgotinib, a once-daily, oral JAK1 preferential inhibitor, under investigation for the treatment of patients with moderately to severely active ulcerative colitis.
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Galapagos increases share capital through subscription right exercises
6/7/2021
Pursuant to the subscription right exercise program of Galapagos’ management board, members of the management board automatically are committed to exercise a minimum number of subscription rights, subject to certain conditions.
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SELECTION study on filgotinib in ulcerative colitis published in The Lancet
6/4/2021
Galapagos NV announced that primary and secondary endpoint results from the phase 3 SELECTIONinduction and maintenance study were published in The Lancet00666-8).The study, sponsored by Gilead Sciences, Inc., was designed to assess the efficacy and safety of the once-daily, oral preferential JAK1 inhibitor, filgotinib, under investigation in patients with moderately to severely active ulcerative colitis.
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Galapagos to present data on rheumatoid arthritis at the upcoming European League Against Rheumatism (EULAR) congress
5/27/2021
Galapagos NV (Euronext & Nasdaq: GLPG) today announced that 15 abstracts,including scientific updates, and data providing further understanding on the profile of filgotinib as a treatment for people with Rheumatoid Arthritis (RA), will be presented at the European League Against Rheumatism (EULAR) virtual congress 2021, 2-5 June.
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Biopharma and life sciences companies from across the globe provide updates on their businesses and pipelines.
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Galapagos announces first patient enrolled in FILOSOPHY study to advance understanding of Jyseleca (filgotinib) effectiveness and safety in a real-world setting
5/18/2021
Study uses mobile device technology to support capture of patient-reported outcomes during early and ongoing use of study treatment amongst patients with rheumatoid arthritis
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Galapagos NV will refocus its clinical pipeline and make some cost adjustments to save the company €150 million after disappointing studies assessing therapies for rheumatoid arthritis and idiopathic pulmonary fibrosis.
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Galapagos refocuses pipeline and rightsizes operations
5/6/2021
Mechelen, Belgium; 06May 2021, 22.01 CET; regulated information – Galapagos NV announces its unaudited Q1results and operational highlights, which are further detailed in theQ12021report available on the Galapagos website, www.glpg.com.
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Galapagos creates new subscription right plans
4/30/2021
Mechelen, Belgium;30 April 2021, 22.01 CET; regulated information –– Galapagos NV announced that its supervisory board created 2,736,250subscription rights under new subscription rightplans for the benefit of the personnelof the company and its subsidiaries.
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Belgium-based Galapagos NV and Foster City, California-based Gilead Sciences halted the ISABELA Phase III clinical trial of ziritaxestat in idiopathic pulmonary fibrosis.
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Selvita completes acquisition of Fidelta from Galapagos
1/4/2021
Galapagos NV and Selvita S.A. announced that the strategic transaction in which Selvita has acquired Fidelta from Galapagos has been completed.
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A little more than one year after Gilead Sciences and Galapagos NV announced intentions to seek regulatory approval for Jyseleca (filgotinib) as a treatment for rheumatoid arthritis, the companies have pulled the plug on that goal.