Xbrane Biopharma has performed a comprehensive in-vitro biosimilarity study with several pilot scale R&D batches of Xlucane versus several batches of the reference product. The study demonstrates no significant difference of Xlucane versus the reference product on the most important parameters. This proves the quality of the product and gives us huge comfort for ongoing scale up of the production to commercial scale and the upcoming clinical trials and it allows us to accelerate the out-licensing process of the product.
In the in-vitro comparability study Xbrane has, in accordance with EMA (European Medicines Agency) and FDA (Food and Drug Administration) biosimilar guidelines, used numerous analytical methods comparing the proteins along 5 key dimensions: primary structure (amino-acid sequence), higher order structure (folding of the protein), binding characteristics (binding with the growth factor VEGFa), biological activity (activity in terms of growth inhibition on living cells) and purity. The study demonstrates no significant difference of Xlucane versus the reference product on the most important dimensions; primary structure, higher order structure, binding characteristics and biological activity. The purity was slightly lower compared to the reference product, which is being addressed through few modifications in the purification process during the scale-up of the production process.
The study will act as a basis for upcoming scientific advice with regulatory authorities to seek guidance on the clinical development strategy for Xlucane and as an important foundation for out-licensing deals with commercialization partners.
"This is a major and significant milestone for us as we now have confirmed that we have a reproducible production process for Xlucane that generates a product proving high biosimilarity in-vitro to the reference product. This gives us full comfort for ongoing scale up of the production to commercial scale and the upcoming clinical trials and it allows us to accelerate the out-licensing process of the product." says Martin Åmark, Xbrane's CEO.
Xlucane is a ranibizumab biosimilar for treatment of Age related Macula Degeneration (AMD), Diabetic Macular Edema (DME) and Retinal Vein Occlusion (RVO). The reference product generates annual sales of 3,6 BUSD and will go off patent 2020 in the US and 2022 in Western Europe.
Xbrane is a commercial phase Swedish biopharmaceutical company specialized in Biosimilars and long acting injectables. Xbrane has world leading expertise in developing generics for long acting injectable drugs and proprietary high-yield protein expression technology for the development of biosimilars. Xbranes's headquarter is located in Stockholm and the company's in-house research and development facilities are in Sweden and Italy. Xbrane is listed at Nasdaq First North since February 3rd, 2016 under the name XBRANE and Avanza Bank AB is Xbrane's certified advisor. For more information seewww.xbrane.com.
For further information, please contact:
Chief Executive Officer
M: +46 (0) 763-093 777
This information is information that Xbrane Biopharma AB (publ) is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact person set out above, at 07:30 February 27 2017.
This announcement is distributed by Nasdaq Corporate Solutions on behalf of Nasdaq Corporate Solutions clients.
The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.
Source: Xbrane Biopharma AB via Globenewswire