China-based Bio‑Thera Solutions (Bio‑Thera) has made a licensing agreement for its bevacizumab copy biological and has started a phase III trial for its tocilizumab copy biological.
Bio-Thera advances bevacizumab and tocilizumab copy biologicals
Biosimilars/News | Posted 01/04/2019 0 Post your comment
Bio-Thera announced on 14 January 2019 that it had reached a licensing agreement with India-based Cipla for its bevacizumab copy biological, BAT1706. Under the agreement Cipla will have exclusive rights to distribute and market the drug in select emerging markets.
Bio-Thera’s BAT1706 is currently in a global phase III study (NCT03329911) in patients with previously untreated advanced non-squamous non-small cell lung cancer. The company says that it intends to file for regulatory approval with China’s National Medical Products Administration (NMPA), the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) in 2020.
On 24 January 2019, Bio-Thera announced that it had started dosing rheumatoid arthritis patients in a global phase III trial for its tocilizumab copy biological, BAT1806. The product is one of four Bio-Thera candidates in phase III trials.
The company says that it is developing a portfolio of ‘innovative and biosimilar molecules’ for various cancers, autoimmune and cardiovascular diseases. The Biologics License Application (BLA) for its adalimumab copy biological, BAT1406, was accepted for review by China’s National Medical Products Administration in August 2018 [1]. The company is also pursuing copy biologicals of ustekinumab, secukinumab and golimumab.
Related articles
Biosimilars of tocilizumab
Reference
1. GaBI Online - Generics and Biosimilars Initiative. Adalimumab copy biologicals accepted for review in China [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2019 Apr 1]. Available from: www.gabionline.net/Biosimilars/News/Adalimumab-copy-biologicals-accepted-for-review-in-China
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 © 2019 Pro Pharma Communications International. All Rights Reserved.
Source: Bio-Thera
Research
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
Biosimilars in inflammatory bowel disease: are we ready for multiple switches
General
Humira's resilience in the face of biosimilar competition
Boehringer Ingelheim to expand access to adalimumab biosimilar
Comments (0)
Post your comment