메뉴 건너뛰기




Volumn 13, Issue 5, 2011, Pages 218-221

Market access of biosimilars: Not only a cost issue

Author keywords

Biopharmaceutical; Biosimilar; Pricing; Registration; Reimbursement

Indexed keywords

ANTINEOPLASTIC AGENT; BIOSIMILAR DRUG; UNCLASSIFIED DRUG;

EID: 79959647129     PISSN: 12923818     EISSN: 17652839     Source Type: Journal    
DOI: 10.1007/s10269-011-2018-8     Document Type: Review
Times cited : (5)

References (19)
  • 2
    • 77951028492 scopus 로고    scopus 로고
    • Biosimilars: Controversies as illustrated by rhGH
    • 20302553 10.1185/03007991003719642 1:CAS:528:DC%2BC3cXkslOisro%3D
    • P.J. Declerck F. Darendeliler M. Goth, et al. 2010 Biosimilars: controversies as illustrated by rhGH Curr Med Res Opin 26 1219 1229 20302553 10.1185/03007991003719642 1:CAS:528:DC%2BC3cXkslOisro%3D
    • (2010) Curr Med Res Opin , vol.26 , pp. 1219-1229
    • Declerck, P.J.1    Darendeliler, F.2    Goth, M.3
  • 3
    • 79952968147 scopus 로고    scopus 로고
    • European Generic Medicines Association. European Generic Medicines Association Brussels
    • European Generic Medicines Association (2010) EGA handbook on biosimilar medicines. European Generic Medicines Association, Brussels
    • (2010) EGA Handbook on Biosimilar Medicines
  • 6
    • 33749345017 scopus 로고    scopus 로고
    • The market for follow-on biologics: How will it evolve?
    • DOI 10.1377/hlthaff.25.5.1291
    • H. Grabowski I. Cockburn G. Long 2006 The market for follow-on biologics: how will it evolve? Health Aff 25 1291 1301 10.1377/hlthaff.25.5.1291 (Pubitemid 44497628)
    • (2006) Health Affairs , vol.25 , Issue.5 , pp. 1291-1301
    • Grabowski, H.1    Cockburn, I.2    Long, G.3
  • 7
    • 77149122380 scopus 로고    scopus 로고
    • Biosimilars: Evidential standards for health technology assessment
    • 20160743 10.1038/clpt.2009.112 1:STN:280:DC%2BC3c7ht1GmsQ%3D%3D
    • D.A. Hughes 2010 Biosimilars: evidential standards for health technology assessment Clin Pharmacol Ther 87 257 261 20160743 10.1038/clpt.2009.112 1:STN:280:DC%2BC3c7ht1GmsQ%3D%3D
    • (2010) Clin Pharmacol Ther , vol.87 , pp. 257-261
    • Hughes, D.A.1
  • 8
    • 0036689918 scopus 로고    scopus 로고
    • Encouraging the use of generic medicines: Implications for transition economies
    • D.R. King P. Kanavos 2002 Encouraging the use of generic medicines: implications for transition economies Croat Med J 43 462 469 12187525 (Pubitemid 34976432)
    • (2002) Croatian Medical Journal , vol.43 , Issue.4 , pp. 462-469
    • King, D.R.1    Kanavos, P.2
  • 10
    • 79952923217 scopus 로고    scopus 로고
    • The future of biosimilars
    • H. Mellstedt 2010 The future of biosimilars Hosp Pharm Eur 49 33 34
    • (2010) Hosp Pharm Eur , vol.49 , pp. 33-34
    • Mellstedt, H.1
  • 11
    • 75149112660 scopus 로고    scopus 로고
    • Strategies for entering the biosimilar market
    • T. Oldham (eds). Biopharm Knowledge Publishing London
    • Oldham T (2006) Strategies for entering the biosimilar market. In: Oldham T (ed) Biosimilars-evolution or revolution? Biopharm Knowledge Publishing, London
    • (2006) Biosimilars-evolution or Revolution?
    • Oldham, T.1
  • 12
    • 77953343625 scopus 로고    scopus 로고
    • Biosimilars: Current status and future directions
    • 20384525 10.1517/14712591003796553 1:CAS:528:DC%2BC3cXnt1ykurs%3D
    • S.D. Roger 2010 Biosimilars: current status and future directions Expert Opin Biol Ther 10 1011 1018 20384525 10.1517/14712591003796553 1:CAS:528:DC%2BC3cXnt1ykurs%3D
    • (2010) Expert Opin Biol Ther , vol.10 , pp. 1011-1018
    • Roger, S.D.1
  • 13
    • 69449095403 scopus 로고    scopus 로고
    • Biosimilar therapeutics-what do we need to consider?
    • 19461855 10.1093/ndtplus/sfn177 1:CAS:528:DC%2BD1MXit1Cht7o%3D
    • H. Schellekens 2009 Biosimilar therapeutics-what do we need to consider? NDT Plus 2 i27 i36 19461855 10.1093/ndtplus/sfn177 1:CAS:528: DC%2BD1MXit1Cht7o%3D
    • (2009) NDT Plus , vol.2
    • Schellekens, H.1
  • 14
    • 79959669045 scopus 로고    scopus 로고
    • Scottish Medicines Consortium. Scottish Medicines Consortium Edinburgh
    • Scottish Medicines Consortium (2010) Epoetin zeta. Scottish Medicines Consortium, Edinburgh
    • (2010) Epoetin Zeta
  • 15
    • 0043248410 scopus 로고    scopus 로고
    • A combined analysis of two pivotal randomized trials of a single dose of pegfilgrastim per chemotherapy cycle and daily Filgrastim in patients with stage II-IV breast cancer
    • 12684649 1:CAS:528:DC%2BD3sXjsVOltLk%3D
    • S. Siena M.J. Piccart F.A. Holmes, et al. 2003 A combined analysis of two pivotal randomized trials of a single dose of pegfilgrastim per chemotherapy cycle and daily Filgrastim in patients with stage II-IV breast cancer Oncol Rep 10 715 724 12684649 1:CAS:528:DC%2BD3sXjsVOltLk%3D
    • (2003) Oncol Rep , vol.10 , pp. 715-724
    • Siena, S.1    Piccart, M.J.2    Holmes, F.A.3
  • 16
    • 77955597659 scopus 로고    scopus 로고
    • Addressing the health technology assessment of biosimilar pharmaceuticals
    • 20649394 10.1185/03007995.2010.505137 1:CAS:528:DC%2BC3cXhtVWqu7fI
    • A. Stewart P. Aubrey J. Belsey 2010 Addressing the health technology assessment of biosimilar pharmaceuticals Curr Med Res Opin 26 2119 2126 20649394 10.1185/03007995.2010.505137 1:CAS:528:DC%2BC3cXhtVWqu7fI
    • (2010) Curr Med Res Opin , vol.26 , pp. 2119-2126
    • Stewart, A.1    Aubrey, P.2    Belsey, J.3
  • 17
    • 79959670245 scopus 로고    scopus 로고
    • The consolidated Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use as amended by Directive 2002/98/EC, Directive 2004/24/EC and Directive 2004/27/EC
    • The consolidated Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use as amended by Directive 2002/98/EC, Directive 2004/24/EC and Directive 2004/27/EC
  • 18
    • 79959661485 scopus 로고    scopus 로고
    • Title VII of the Patient Protection and Affordable Care Act of 2010, Improving Access to Innovative Medical Therapies-Subtitle (Biologics Price Competition and Innovation Act of 2009, section 351(k), 351 (l), 351(m). Pub.L.No.111-48. 2011. 3-2-2011
    • Title VII of the Patient Protection and Affordable Care Act of 2010, Improving Access to Innovative Medical Therapies-Subtitle (Biologics Price Competition and Innovation Act of 2009, section 351(k), 351 (l), 351(m). Pub.L.No.111-48. 2011. 3-2-2011
  • 19
    • 77249086523 scopus 로고    scopus 로고
    • Biosimilars approval process
    • 19925842 10.1016/j.yrtph.2009.11.004
    • L. Zuniga B. Calvo 2010 Biosimilars approval process Regul Toxicol Pharmacol 56 374 377 19925842 10.1016/j.yrtph.2009.11.004
    • (2010) Regul Toxicol Pharmacol , vol.56 , pp. 374-377
    • Zuniga, L.1    Calvo, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.