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  • ||||||||||  namodenoson (CF102) - Can / Fite, piclidenoson (CF101) - Can / Fite
    Review, Journal:  Adenosine A3 Receptor: From Molecular Signaling to Therapeutic Strategies for Heart Diseases. (Pubmed Central) -  Jun 19, 2024   
    Several A3AR-specific agonists, such as piclidenoson and namodenoson, exert cardioprotective impacts during ischemia in the diverse animal models of heart disease. Thus, modulating A3ARs serves as a potential therapeutic approach, fueling considerable interest in developing compounds that target A3ARs as potential treatments for heart diseases.
  • ||||||||||  namodenoson (CF102) - Can / Fite
    Journal:  Gene regulation in activated microglia by adenosine A receptor agonists: a transcriptomics study. (Pubmed Central) -  Jun 18, 2024   
    Analysis of known and predicted protein-protein interactions showed that Smad3 and Sp1 are transcription factors whose genes are regulated by AR activation. Under the conditions of cell activation and agonist treatment regimen, 2-Cl-IB-MECA did not lead to any tendency to favor the expression of genes related to neuroprotective microglia (M2).
  • ||||||||||  Cejemly (sugemalimab) / CStone Pharma
    Sugemalimab in locally advanced and advanced Chinese NSCLC: A real-world retrospective study. () -  Apr 24, 2024 - Abstract #ASCO2024ASCO_5889;    
    Our study demonstrated Sugemalimab-based therapy provide clinical benefits to LA-NSCLC and mNSCLC with good safety in real-world setting. The combination treatment of Sugemalimab with radiotherapy illustrates low pulmonary toxicity and superior tolerability.
  • ||||||||||  Remicade (infliximab) / J&J, Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    Trial completion date, Trial primary completion date, Adverse events, Combination therapy, Metastases:  PD-1 Antibody Therapy + Infliximab for Metastatic Melanoma (clinicaltrials.gov) -  Mar 21, 2024   
    P2,  N=36, Recruiting, 
    The combination treatment of Sugemalimab with radiotherapy illustrates low pulmonary toxicity and superior tolerability. Trial completion date: Jun 2025 --> Jun 2026 | Trial primary completion date: Jun 2023 --> Jun 2025
  • ||||||||||  Remicade (infliximab) / J&J, Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    Trial completion date, Trial primary completion date, Checkpoint inhibition:  Infliximab for Treatment of Immune Checkpoint Inhibitor Colitis (clinicaltrials.gov) -  Mar 15, 2024   
    P2,  N=42, Recruiting, 
    Trial completion date: Jun 2025 --> Jun 2026 | Trial primary completion date: Jun 2023 --> Jun 2025 Trial completion date: Jun 2023 --> Jun 2030 | Trial primary completion date: Jun 2023 --> Jun 2030
  • ||||||||||  hyoscine butylbromide oral / Generic mfg.
    Preclinical, Journal:  Vanillin derivatives as antiamnesic agents in scopolamine-induced memory impairment in mice. (Pubmed Central) -  Feb 29, 2024   
    inhibitors (originator drugs and biosimilars) might predict the response to therapy at 4 years in patients with long-standing rheumatoid arthritis. The compounds; SB-1, SB-3, SB-4 and SB-6 more potently inhibited AChE with IC50 values of 0.078, 0.157, 0.108, and 0.014
  • ||||||||||  Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    The Biosimilar Switch: IBD nurse's experience in Our Lady of Lourdes Hospital (Poster exhibition) -  Jan 25, 2024 - Abstract #ECCOIBD2024ECCO_IBD_1375;    
    Results 86 patients were switched from the originator to the biosimilar Flixabi...Conclusion Of the 86 patients who were switched 22 responded to the questionnaire. 21 patients were happy with their overall experience with how the switch was conducted.
  • ||||||||||  Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    Reimbursement, US reimbursement, Journal, Medicare:  Filgrastim and infliximab biosimilar uptake in Medicare Advantage compared with Traditional Medicare, 2016-2019. (Pubmed Central) -  Jan 2, 2024   
    Our findings suggest that filgrastim and infliximab biosimilar uptake is greater in MA compared with Traditional Medicare, which is driven in part by particularly high uptake of biosimilars in MA Kaiser HMO plans. This highlights the need for future work to examine specific strategies and levers employed by MA Kaiser HMO plans and other insurers to increase biosimilar uptake, which can lead to cost savings for physician-administered drugs.
  • ||||||||||  Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    Journal:  Outcomes of the use of infliximab biosimilars in rheumatology and gastroenterology clinics. (Pubmed Central) -  Jan 2, 2024   
    We conclude that the effort to convert clinically stable patients to a biosimilar product resulted in a significant increase in biosimilar use within the health system. This is thought to have resulted in significant financial advantages both to our institution as well as patients, without sacrificing overall clinical control.
  • ||||||||||  Enrollment status, Trial completion date, Trial primary completion date:  FREE: De-escalation of Anti-TNF Therapy in Inflammatory Bowel Disease (clinicaltrials.gov) -  Nov 30, 2023   
    P4,  N=148, Enrolling by invitation, 
    Seven scanbodies (SB1, SB2, SB3, SB4, SB5, SB6, and SB7) and four intraoral scanners (Primescan Recruiting --> Enrolling by invitation | Trial completion date: Jun 2023 --> Mar 2025 | Trial primary completion date: Jun 2023 --> Mar 2025
  • ||||||||||  Eticovo (etanercept-ykro) / Biogen, Organon, Samsung, Ewopharma, Yuhan Corp, Mundipharma
    Journal:  Comparative Analysis of Anticonvulsant Activity of Trans and Cis 5,5'-Diphenylhydantoin Schiff Bases. (Pubmed Central) -  Nov 29, 2023   
    Our results suggest that trans-cis conversion of 5,5'-diphenylhydantoin Schiff bases has potential against seizure spread in the MES test and mitigated the KA-induced SE. The antioxidant potency of cisSB4-Ph might be associated with its efficacy in mitigating the SE.
  • ||||||||||  phenytoin / Generic mfg.
    Journal:  Additive Anticonvulsant Profile and Molecular Docking Analysis of 5,5'-Diphenylhydantoin Schiff Bases and Phenytoin. (Pubmed Central) -  Nov 25, 2023   
    These data, combined with the worst interaction energies of our ligands with the mu receptor, suggest that the primary mechanism of their action involves the kappa and delta receptors, where the selectivity to the kappa receptor leads to higher biological effects. Our findings suggest that the four Schiff bases might be promising candidates with potential applications as a safe and effective adjuvant in epilepsy.
  • ||||||||||  Remicade (infliximab) / Merck (MSD), Mitsubishi Tanabe, J&J, Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    Enrollment open, Trial initiation date:  REMODEL-CD: Precise Infliximab Exposure and Pharmacodynamic Control (clinicaltrials.gov) -  Jul 20, 2023   
    P2/3,  N=180, Recruiting, 
    Because user-friendly devices can improve treatment adherence, pharmaceutical companies should consider patient convenience when developing medical devices. Not yet recruiting --> Recruiting | Initiation date: Apr 2023 --> Jul 2023
  • ||||||||||  Trial completion date, Trial initiation date, Trial primary completion date:  CAMEO: Clinical, Imaging, and Endoscopic Outcomes of Children Newly Diagnosed With Crohn's Disease (clinicaltrials.gov) -  Apr 24, 2023   
    P=N/A,  N=900, Not yet recruiting, 
    SB2 was safe and effective in IFX-na Trial completion date: Apr 2029 --> Jul 2029 | Initiation date: Apr 2023 --> Jul 2023 | Trial primary completion date: Apr 2028 --> Jul 2028
  • ||||||||||  Eticovo (etanercept-ykro) / Biogen, Organon, Samsung, Ewopharma, Yuhan Corp, Mundipharma
    An Evaluation of Patient Experience of the Belfast Health and Social Care Trust Rheumatology Etanercept Biosimilar Switch Programme. (Poster View) -  Apr 2, 2023 - Abstract #EULAR2023EULAR_2460;    
    Background The Belfast Health and Social Care Trust Rheumatology department commenced a biosimilar switch programme in July 2019, switching patients from Etanercept (Enbrel) to biosimilar (Benepali)...Conclusion The Etanercept biosimilar switch programme was successful with high switch rates, high levels of patient confidence and satisfaction. Recommendations for future include improving the process of shared decision-making during consultation to ensure fully informed patient consent.
  • ||||||||||  Eticovo (etanercept-ykro) / Samsung, Merck (MSD), Ewopharma, Yuhan Corp, Mundipharma, Biogen
    Review, Journal:  Managing spot blotch disease in wheat: Conventional to molecular aspects. (Pubmed Central) -  Mar 10, 2023   
    Despite, marker assisted breeding for SB resistance in wheat is scarce. Better understanding of wheat genome assemblies, functional genomics and cloning of resistance genes will further accelerate breeding for SB resistance in wheat.
  • ||||||||||  Remicade (infliximab) / Merck (MSD), Mitsubishi Tanabe, J&J, Renflexis (infliximab-abda) / Yuhan Corp, Biogen, Ewopharma, Samsung, Organon
    New P2/3 trial:  REMODEL-CD: Precise Infliximab Exposure and Pharmacodynamic Control (clinicaltrials.gov) -  Dec 21, 2022   
    P2/3,  N=180, Not yet recruiting, 
  • ||||||||||  Eticovo (etanercept-ykro) / Samsung, Merck (MSD), Ewopharma, Yuhan Corp, Mundipharma, Biogen
    Observational data, Journal:  Outcome of adult patients with JIA treated with the biosimilar Benepali: results of the biologic register JuMBO. (Pubmed Central) -  Dec 16, 2022   
    Tolerability and effectiveness of the biosimilar Benepali were satisfactory and therapy survival was comparable to the originator. Further data on therapy with biologics and biosimilars such as Benepali must be collected by registries such as BiKeR and JuMBO in order to optimize therapy and patient outcomes and to reduce costs in the health system in the long term.