BioOutsource launches ready-to-use biosimilarity assays

Biosimilars/News | Posted 15/04/2016 post-comment0 Post your comment

Sartorius Stedim BioOutsource (BioOutsource), a subsidiary of Sartorius Stedim Biotech, has launched a range of ready-to-use assays for testing biosimilarity. The assays are available for biosimilars of Hoffmann–La Roche/Chugai’s rheumatoid arthritis treatment Actemra (tocilizumab), Centocor’s psoriasis treatment Stelara (ustekinumab) and Novartis/Genentech’s age-related macular degeneration drug Lucentis (ranibizumab).

picture 147

The assays are designed to ensure accurate, rapid and cost-effective comparability results for these biosmilars, and include tocilizumab IL-6R neutralization bioassays; a tocilizumab IL-6R binding ELISA; ustekinumab IL-12/IL-23 binding assays; a ustekinumab C1Q binding assay; a ustekinumab neutralization bioassay; ranibizumab VEGF binding assays and a ranibizumab VEGF neutralization bioassay.

Dr Daniel Galbraith, Chief Scientific Officer of BioOutsource, commented that biopharamceutical companies will benefit from a comprehensive range of ready-to-use assays that can be trusted to determine precise comparability results and to expedite drug development programmes.

BioOutsource already has an existing portfolio of assays, and the new additions bring the total molecules supported by the company to nine. BioOutsource is a provider of contract testing services and its R & D Department offers customized assay configuration services to meet specific requirements.

Scottish-based BioOutsource, a provider of contract testing services to monitor the safety and quality of biological drugs and vaccines, was acquired by Sartorius Stedim Biotech in 2015 to better support their global biopharmaceutical clients in fast-tracking new drugs.

Related article
Biosimilars on the horizon

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2016 Pro PharmaCommunications International. All Rights Reserved.

Source: Sartorius Stedim Biotech

comment icon Comments (0)
Post your comment
Related content
Canada approves pegfilgrastim biosimilar Armlupeg
Pegfilgrastim DrugBank V18K30
Biosimilars/News Posted 20/11/2024
FDA approves fifth ustekinumab biosimilar Imuldosa
11453696_l
Biosimilars/News Posted 13/11/2024
Most viewed articles
About GaBI
Home/About GaBI Posted 06/08/2009
EU guidelines for biosimilars
EMA logo 1 V13C15
Home/Guidelines Posted 08/10/2010