Positive phase III results for etanercept biosimilar

Biosimilares/Investigación | Posted 27/11/2015 post-comment0 Post your comment

On 9 November 2015, biopharmaceutical specialists Coherus and Baxalta (a spin-off company from Baxter International) announced positive results from a phase III study of its etanercept biosimilar (CHS-0214).

Etanercept V14H14

The phase III, randomized, double-blind, parallel group, active-control, multicentre study was designed to compare the efficacy and safety of candidate etanercept biosimilar (CHS-0214) versus Enbrel (etanercept) in subjects with chronic plaque psoriasis. The RHAPSODY trial was planned to be completed in July 2015.

The efficacy endpoints were based on a Week 12 assessment of Psoriasis Area and Severity Index (PASI) scores. At Week 12, the primary endpoints, the mean per cent change in PASI from baseline and the proportion of subjects achieving 75% improvement in PASI from baseline, were within the pre-specified margins, which the companies claim ‘demonstrates equivalence of CHS-0214 compared to Enbrel’. The companies also claim that there were ‘no clinically meaningful differences in the safety profiles of the products’.

The study is still ongoing and will continue as planned until Week 52. According to ClinicalTrials.gov, Coherus is also carrying out a phase III trial of its etanercept biosimilar in patients with rheumatoid arthritis, as well as a long-term extension study. These confirmatory trials are intended for inclusion in global marketing applications for CHS-0214. Results for the phase III study in patients with rheumatoid arthritis are expected in the first quarter of 2016.

Coherus and Baxalta (then part of Baxter) initiated a collaboration to develop and commercialize CHS-0214 back in September 2013 [1].

South Korean electronics giant Samsung and biotechnology company Biogen Idec’s joint venture Samsung Bioepis is the closest to having an etanercept biosimilar approved in the European Union. The company announced in January 2015 that its etanercept biosimilar candidate, SB4, had been accepted for review by the European Medicines Agency (EMA) [2].

Editor’s comment
It should be noted that data of the study presented in this article were published as a press release. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.

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References
1.   GaBI Online - Generics and Biosimilars Initiative. Baxter and Coherus to collaborate on biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2015 Nov 27]. Available from: http://www.gabionline.net/Biosimilars/News/Baxter-and-Coherus-to-collaborate-on-biosimilars
2.   GaBI Online - Generics and Biosimilars Initiative. Biosimilar etanercept submitted for approval in EU [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2015 Nov 27]. Available from: www.gabionline.net/Biosimilars/News/Biosimilar-etanercept-submitted-for-approval-in-EU

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Source: Baxalta,ClinicalTrials.gov, Coherus

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