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hans c. ebbers
标题
引用次数
引用次数
年份
Interchangeability, immunogenicity and biosimilars
HC Ebbers, SA Crow, AG Vulto, H Schellekens
Nature biotechnology 30 (12), 1186-1190, 2012
1372012
The safety of switching between therapeutic proteins
HC Ebbers, M Muenzberg, H Schellekens
Expert opinion on biological therapy 12 (11), 1473-1485, 2012
1372012
The efficacy, safety, and immunogenicity of switching between reference biopharmaceuticals and biosimilars: a systematic review
L Barbier, HC Ebbers, P Declerck, S Simoens, AG Vulto, I Huys
Clinical Pharmacology & Therapeutics 108 (4), 734-755, 2020
1322020
Antibody-mediated pure red cell aplasia in chronic kidney disease patients receiving erythropoiesis-stimulating agents: new insights
IC Macdougall, SD Roger, A De Francisco, DJA Goldsmith, H Schellekens, ...
Kidney international 81 (8), 727-732, 2012
1322012
Use of the conditional marketing authorization pathway for oncology medicines in Europe
J Hoekman, WPC Boon, JC Bouvy, HC Ebbers, JP de Jong, ML De Bruin
Clinical Pharmacology & Therapeutics 98 (5), 534-541, 2015
702015
Biosimilars: in support of extrapolation of indications
HC Ebbers
Journal of Crohn's and Colitis 8 (5), 431-435, 2014
642014
Are we ready to close the discussion on the interchangeability of biosimilars?
HC Ebbers, H Schellekens
Drug Discovery Today 24 (10), 1963-1967, 2019
512019
Interchangeability. An insurmountable fifth hurdle?
HC Ebbers, P Chamberlain
Generics and Biosimilars Initiative Journal 3 (2), 88-97, 2014
402014
Real-world evidence on etanercept biosimilar SB4 in etanercept-naïve or switching patients: a systematic review
HC Ebbers, B Pieper, A Issa, J Addison, U Freudensprung, MF Rezk
Rheumatology and Therapy 6, 317-338, 2019
392019
Contribution of animal studies to evaluate the similarity of biosimilars to reference products
PJK van Meer, HC Ebbers, M Kooijman, CC Gispen-de Wied, ...
Drug discovery today 20 (4), 483-490, 2015
302015
Measures of biosimilarity in monoclonal antibodies in oncology: the case of bevacizumab
HC Ebbers, PJK van Meer, EHM Moors, AK Mantel-Teeuwisse, ...
Drug Discovery Today 18 (17-18), 872-879, 2013
302013
Today’s challenges in pharmacovigilance: what can we learn from epoetins?
HC Ebbers, AK Mantel-Teeuwisse, EHM Moors, H Schellekens, ...
Drug safety 34, 273-287, 2011
292011
Controversies in establishing biosimilarity: extrapolation of indications and global labeling practices
HC Ebbers, P Chamberlain
BioDrugs 30, 1-8, 2016
282016
Effective pharmaceutical regulation needs alignment with doctors
HC Ebbers, T Pieters, HG Leufkens, H Schellekens
Drug discovery today 17 (3-4), 100-103, 2012
272012
Differences between post-authorization adverse drug reactions of biopharmaceuticals and small molecules
HC Ebbers, E Al-Temimi, EHM Moors, AK Mantel-Teeuwisse, ...
BioDrugs 27, 167-174, 2013
252013
The role of Periodic Safety Update Reports in the safety management of biopharmaceuticals
HC Ebbers, AK Mantel-Teeuwisse, FA Sayed-Tabatabaei, EHM Moors, ...
European journal of clinical pharmacology 69, 217-226, 2013
222013
The Cost‐Effectiveness of Periodic Safety Update Reports for Biologicals in Europe
JC Bouvy, HC Ebbers, H Schellekens, MA Koopmanschap
Clinical Pharmacology & Therapeutics 93 (5), 433-442, 2013
202013
A cohort study exploring determinants of safety-related regulatory actions for biopharmaceuticals
HC Ebbers, AK Mantel-Teeuwisse, EHM Moors, FAS Tabatabaei, ...
Drug safety 35, 417-427, 2012
162012
An introduction to biosimilars for the treatment of retinal diseases: a narrative review
SM Hariprasad, RP Gale, CY Weng, HC Ebbers, MF Rezk, R Tadayoni
Ophthalmology and Therapy 11 (3), 959-982, 2022
152022
The effect of exposure misclassification in spontaneous ADR reports on the time to detection of product‐specific risks for biologicals: a simulation study
NS Vermeer, HC Ebbers, SMJM Straus, HGM Leufkens, TCG Egberts, ...
pharmacoepidemiology and drug safety 25 (3), 297-306, 2016
132016
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