עקוב אחר
hans c. ebbers
hans c. ebbers
כתובת אימייל מאומתת בדומיין uu.nl
כותרת
צוטט על ידי
צוטט על ידי
שנה
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
1362012
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
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
1302020
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
Controversies in establishing biosimilarity: extrapolation of indications and global labeling practices
HC Ebbers, P Chamberlain
BioDrugs 30, 1-8, 2016
282016
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
282011
Effective pharmaceutical regulation needs alignment with doctors
HC Ebbers, T Pieters, HG Leufkens, H Schellekens
Drug discovery today 17 (3-4), 100-103, 2012
262012
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
212013
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
192013
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
152012
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
142022
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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מאמרים 1–20