TNF inhib 
Welcome,         Profile    Billing    Logout  
 10 Companies  10 Products   10 Products   667 Diseases   132 Trials   5551 News 


12345678910111213...224225»
  • ||||||||||  Remicade (infliximab) / J&J
    Review, Journal:  Management of anal fistulas in Crohn (Pubmed Central) -  May 15, 2024   
    Anal fistulas in Crohn's disease are a real therapeutic challenge. New medical and surgical therapies are currently being evaluated, with promising results.
  • ||||||||||  Skyrizi (risankizumab-rzaa) / AbbVie, Boehringer Ingelheim
    Journal, Real-world evidence, Real-world:  Long-term outcome of risankizumab in Crohn's disease: a real-world GETAID study. (Pubmed Central) -  May 11, 2024   
    This is the first real-life study to report long-term outcomes in patients with refractory CD treated with risankizumab. Half of the patients achieved steroid-free clinical remission after one year, and the safety profile was consistent with the literature.
  • ||||||||||  Remicade (infliximab) / J&J
    Perception of Pediatric Gastrointestinal Specialists on Anti -tumor Necrosis Factor Therapy in Patients with Pediatric Crohn's Disease (Studio 8-9 (6F)) -  May 10, 2024 - Abstract #IMKASID2024IMKASID_344;    
    Regarding the selection between infliximab and adalimumab, the main factors affecting decisions were disease severity of the patient (40.5%), preference of the patient (23.8%), quick resolution of clinical symptoms and laboratory results (21.4%), and injection route and intervals of the drugs (14.3%)...Conclusion : The majority of pediatric GI specialists considered an upfront or accelerated step-up approach as the appropriate treatment strategy for pediatric CD. The Korean national insurance policy should be able to support the perception of Korean pediatric GI specialists
  • ||||||||||  Skyrizi (risankizumab-rzaa) / AbbVie, Boehringer Ingelheim, Stelara (ustekinumab) / J&J
    Risankizumab versus Ustekinumab for Patients with Moderate to Severe Crohn's Disease: Results from the Phase 3b SEQUENCE Study (Studio 8-9 (6F)) -  May 10, 2024 - Abstract #IMKASID2024IMKASID_262;    
    Conclusion : In pts with moderate to severe CD who failed anti-TNF therapy, RZB demonstrated non-inferiority to UST in achieving wk24 clinical remission, superiority in achieving wk48 endoscopic remission, and superiority for achieving all secondary endpoints. The safety profiles of RZB and UST were consistent with previously published results.
  • ||||||||||  Retrospective data, Review, Journal, Metastases:  Meta-analysis: Persistence of advanced therapies in the treatment of inflammatory bowel disease. (Pubmed Central) -  May 7, 2024   
    Chronic continuous type and previous anti-TNF and VDZ exposure negatively contributed to short-term effectiveness, whereas short-term effectiveness provided good persistency. This meta-analysis highlights the superior persistence of ustekinumab and vedolizumab over TNFi, and offers valuable insights for clinicians navigating the challenging landscape of UC and CD therapeutic choices.
  • ||||||||||  Journal:  Gut microbiome and metabolome to discover pathogenic bacteria and probiotics in ankylosing spondylitis. (Pubmed Central) -  May 7, 2024   
    Through experimental studies, the relationship between microbes and metabolites was further confirmed, and the impact of these two types of microbes on the enterocytes and the inflammatory cytokine interleukin-18 (IL-18) was explored. In summary, multi-omics exploration elucidated the impact of TNFi on the gut microbiota and metabolites and proposed a novel therapeutic perspective: supplementation of compounds to inhibit potential pathogenic bacteria and to promote potential probiotics, therefore controlling inflammation in AS.
  • ||||||||||  Journal:  Transcriptomic network analysis reveals key drivers of response to anti-TNF biologics in patients with rheumatoid arthritis. (Pubmed Central) -  May 2, 2024   
    Across ASAS outcomes, bimekizumab was comparable with most b/tsDMARDs, including ixekizumab, TNF inhibitors and upadacitinib, and achieved higher response rates vs secukinumab for some ASAS outcomes in predominantly b/tsDMARD-na This study provides response-specific treatment-induced transcriptomic signatures by comparing the transcriptomic landscape between patients with excellent and null responses to anti-TNF drugs at both gene and network levels.
  • ||||||||||  Humira (adalimumab) / AbbVie
    Journal:  Risk factors for development of anti-adalimumab antibodies in non-infectious uveitis. (Pubmed Central) -  May 2, 2024   
    History of interruption in anti-TNF therapy and flare during adalimumab were associated with development of AAA, while weekly dosing of adalimumab was protective against AAA. Identification of those with higher risk of developing AAA may guide in clinical decision making to optimize management for these patients.
  • ||||||||||  Journal:  Weight loss affects disease activity and treatment response in inflammatory rheumatic diseases. (Pubmed Central) -  May 1, 2024   
    Screening and management of obesity are part of the dietary recommendations of the French Society for Rheumatology in patients with chronic inflammatory rheumatic diseases. Of course, this should be combined with others lifestyle modifications such as smoking cessation, higher food quality, increased physical activity and reduced sedentary behavior.
  • ||||||||||  Remicade (infliximab) / J&J, Actemra IV (tocilizumab) / Roche, JW Pharma, Humira (adalimumab) / AbbVie
    EFFICACY AND DRUG SURVIVAL OF BIOLOGIC AGENTS IN BEHCET'S DISEASE: A REAL-LIFE OBSERVATIONAL MONOCENTRIC STUDY (Station 08) -  May 1, 2024 - Abstract #AUTO2024AUTO_266;    
    The aim is to assess their effectiveness and 10-year retention rate.Methods We included patients treated with Infliximab (IFX), Adalimumab (ADA), Apremilast (APR), and Tocilizumab (TCZ) between 2009-2023...Previous administration of colchicine was more frequent in patients treated with APR (p=0.035)...Daily prednisone dose was significantly reduced with IFX (10[5-21.25]vs5[0-10],p=0.015), while no differences were noted in acute phase reactants...Discontinuation of bDMARDs was due to intolerance (3.7%), remission (3.7%) and adverse events (15.1%). conclusions :bDMARDs treatment is effective and its retention rate is affected by female sex, but not by concomitant cDMARDs.