Zobrazeno 1 - 10
of 2 437
pro vyhledávání: '"L. Peyrin‐Biroulet"'
Autor:
S Vieujean, J O Lindsay, D Rubin, F D’Amico, V Ahuja, M S Silverberg, A Sood, J K Yamamoto-Furusho, M Nagahori, M Watanabe, I E Koutroubakis, K Foteinogiannopoulou, A Walsh, A Outtier, M T Abreu, M Dubinsky, C Siegel, E Louis, I Dotan, W Reinisch, S Danese, L Peyrin-Biroulet
Publikováno v:
Journal of Crohn's and Colitis. 17:i794-i797
Background Recruitment rates for phase 2b/3 randomized controlled trials (RCTs) in IBD have substantially dropped over time. Several steps are required prior to successful patient randomization. Initially the physician must propose a trial to a poten
Autor:
B G Feagan, K Matsuoka, G Rogler, M Faes, A Oortwijn, A de Haas, C Rudolph, L Peyrin-Biroulet
Publikováno v:
Journal of Crohn's and Colitis. 17:i47-i50
Background Filgotinib (FIL) is a once-daily, oral, Janus kinase 1 preferential inhibitor approved for the treatment of ulcerative colitis (UC). FIL 200 mg (FIL200) was effective in inducing and maintaining clinical remission vs placebo (PBO) and well
Autor:
J van der Woude, S Schreiber, L Peyrin-Biroulet, Z Szekanecz, E H Choy, P J Stiers, P Van Hoek, K Van Beneden, A de Haas, C Rudolph, H ten Cate
Publikováno v:
Journal of Crohn's and Colitis. 17:i646-i649
Background The once-daily, oral, Janus kinase 1 preferential inhibitor filgotinib (FIL) is approved for the treatment of moderately to severely active rheumatoid arthritis (RA) and ulcerative colitis (UC) in the UK, the EU and Japan.1 To further unde
Autor:
B Sands, L Peyrin-Biroulet, S Danese, D T Rubin, S Vermeire, O Laurent, A Luo, D Nguyen, J D Lu, A Wiechowska-Kozlowska, J Leszczyszyn, R Kempinski, J Kierkus, C Ma, T Ritter, B G Feagan, S Targan
Publikováno v:
Journal of Crohn's and Colitis. 17:i56-i59
Background Tumor necrosis factor-like cytokine 1A (TL1A) is an upstream regulator of pro-inflammatory cytokines and fibrosis signals. PRA023 is an anti-TL1A monoclonal antibody in development for multiple inflammatory/fibrotic diseases using a precis
Autor:
V Jairath, G Zou, G Radulescu, J Sigler, S C Mcfarlane, S Adsul, M Freire, L Peyrin-Biroulet, J F Colombel, G W Moran, S Sebastian, S Travis, S Vermeire, W J Sandborn, G R D’Haens, B G Feagan
Publikováno v:
Journal of Crohn's and Colitis. 17:i826-i829
Background Symptoms, endoscopy, histology, and biomarkers are used to evaluate disease activity and response to therapy in ulcerative colitis (UC). Histologic disease activity may persist in ~25% of patients with normal-appearing endoscopic mucosa, a
Autor:
S Vermeire, S Danese, B L Cohen, F Magro, Y Chen, C Ha, E Dubcenco, A P Lacerda, E Marced, J Oomen, A Garrison, L Peyrin-Biroulet
Publikováno v:
Journal of Crohn's and Colitis. 17:i510-i513
Background Improvement in clinical outcomes and normalisation of objective markers of inflammation, high-sensitivity C-reactive protein (hs-CRP) and faecal calprotectin (FCP), are considered treatment targets per STRIDE-II guidelines.1 We evaluated t
Autor:
J Van Oostrom, S Anjie, M Braad, J Horrigan, N Karimi, B Adi, G Ganesh, S K Yang, J Lasa, C Broër, A de Kruif, P Olivera Sendra, B D Ye, R Banerjee, S Connor, C Siegel, L Peyrin-Biroulet, K Gecse, G D'Haens
Publikováno v:
Journal of Crohn's and Colitis. 17:i337-i339
Background For patients living with inflammatory bowel diseases (IBD), the ultimate treatment goal is “normal life”. However, no patient-reported outcome measurement (PROM) exists to measure the level of life normality in IBD. We previously asked
Autor:
L Peyrin-Biroulet, G Parkes, C Rodríguez, J Siffledeen, J Wright, E Broide, S Ford, A P Lacerda, J Oomen, A Garrison, S Berg, D T Rubin
Publikováno v:
Journal of Crohn's and Colitis. 17:i20-i22
Background Biologic therapies are used to treat moderate-to-severe Crohn’s Disease (CD), but many patients eventually lose response to them. With new potential therapies for CD, understanding their efficacy after patients undergo biologic treatment
Autor:
S Schreiber, W Reinisch, D Nguyen, T Guerin, J Kierkus, P Rozpondek, D Bourdet, B Abhyankar, L Peyrin-Biroulet
Publikováno v:
Journal of Crohn's and Colitis. 17:i505-i507
Background The unmet need in Crohn’s disease (CD) exists for new medications with an optimized risk-benefit ratio with avoidance of systemic side effects. This Phase 2 study evaluated the efficacy and safety of the oral, once-daily, gut-selective p
Autor:
R Atreya, P Irving, M Fujiya, J F Colombel, S Danese, L Peyrin-Biroulet, T Bessissow, R Panaccione, G D’Haens, S van Haaren, E Neimark, J Zambrano, Y Zhang, K Kligys, M Ferrante
Publikováno v:
Journal of Crohn's and Colitis. 17:i675-i677
Background In the risankizumab (RZB) phase 3 clinical programme, Crohn’s disease (CD) patients who responded to RZB intravenous (IV) induction were re-randomised to RZB or placebo (PBO) (withdrawal PBO subcutaneous [SC] in maintenance (FORTIFY), wh