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Journal Abstract Search
295 related items for PubMed ID: 29285735
21. [Immunogenicity of biosimilars]. van Aerts LA, Franken AA, Leufkens HG. Ned Tijdschr Geneeskd; 2016; 160():D888. PubMed ID: 28000573 [Abstract] [Full Text] [Related]
22. Neutralizing Antibody Assay Development with High Drug and Target Tolerance to Support Clinical Development of an Anti-TFPI Therapeutic Monoclonal Antibody. Xiang Y, Parng C, Olson K, Seletskaia E, Gorovits B, Jani D, Caiazzo T, Joyce A, Donley J. AAPS J; 2019 Mar 29; 21(3):46. PubMed ID: 30927117 [Abstract] [Full Text] [Related]
23. The Language of Biosimilars: Clarification, Definitions, and Regulatory Aspects. Declerck P, Danesi R, Petersel D, Jacobs I. Drugs; 2017 Apr 29; 77(6):671-677. PubMed ID: 28258517 [Abstract] [Full Text] [Related]
24. Comparability of Antibody-Mediated Cell Killing Activity Between a Proposed Biosimilar RTXM83 and the Originator Rituximab. Cuello HA, Segatori VI, Alberto M, Pesce A, Alonso DF, Gabri MR. BioDrugs; 2016 Jun 29; 30(3):225-31. PubMed ID: 27053342 [Abstract] [Full Text] [Related]
25. The use of pharmacometrics to optimize biosimilar development. Dodds M, Chow V, Markus R, Pérez-Ruixo JJ, Shen D, Gibbs M. J Pharm Sci; 2013 Nov 29; 102(11):3908-14. PubMed ID: 24027111 [Abstract] [Full Text] [Related]
26. Biosimilars in ulcerative colitis: When and for who? Ilias A, Gonczi L, Kurti Z, Lakatos PL. Best Pract Res Clin Gastroenterol; 2018 Nov 29; 32-33():35-42. PubMed ID: 30060937 [Abstract] [Full Text] [Related]
27. An update on the animal studies conducted for biosimilar approvals - Regulatory requirement vs actual scenario. Pipalava P, Patel R, Mehta M, Dahiya M, Singh I, Jose V. Regul Toxicol Pharmacol; 2019 Oct 29; 107():104415. PubMed ID: 31254556 [Abstract] [Full Text] [Related]
32. Efficacy and Safety Outcomes for Originator TNF Inhibitors and Biosimilars in Rheumatoid Arthritis and Psoriasis Trials: A Systematic Literature Review. Moots RJ, Curiale C, Petersel D, Rolland C, Jones H, Mysler E. BioDrugs; 2018 Jun 29; 32(3):193-199. PubMed ID: 29790131 [Abstract] [Full Text] [Related]
33. An introduction to biosimilar cancer therapeutics: definitions, rationale for development and regulatory requirements. Buske C, Ogura M, Kwon HC, Yoon SW. Future Oncol; 2017 May 29; 13(15s):5-16. PubMed ID: 28482702 [Abstract] [Full Text] [Related]
36. Key considerations in the preclinical development of biosimilars. Bui LA, Hurst S, Finch GL, Ingram B, Jacobs IA, Kirchhoff CF, Ng CK, Ryan AM. Drug Discov Today; 2015 May 29; 20 Suppl 1():3-15. PubMed ID: 25912284 [Abstract] [Full Text] [Related]
37. Current Perspectives on Ligand-Binding Assay Practices in the Quantification of Circulating Therapeutic Proteins for Biosimilar Biological Product Development. Thway TM, Wang YM, Booth BP, Maxfield K, Huang SM, Zineh I. AAPS J; 2019 Dec 19; 22(1):15. PubMed ID: 31858313 [Abstract] [Full Text] [Related]
40. An Integrated Approach for a Structural and Functional Evaluation of Biosimilars: Implications for Erythropoietin. Gianoncelli A, Bonini SA, Bertuzzi M, Guarienti M, Vezzoli S, Kumar R, Delbarba A, Mastinu A, Sigala S, Spano P, Pani L, Pecorelli S, Memo M. BioDrugs; 2015 Aug 19; 29(4):285-300. PubMed ID: 26334631 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]