11 Jan 2021 Xbrane Biopharma AB (publ) (“Xbrane” or “the company”) Xbrane has additionally four biosimilars in its pipeline targeting €8.7b in originator 

Xbrane have six more products in the pipeline that are in earlier phases of clinical development. As Head of CMC Regulatory Affairs you manage the entire 

Xbrane är noterat på Nasdaq Stockholm under kortnamnet XBRANE. För mer information besök www.xbrane.com. The company’s pipeline consists of a wide range of development candidates originated from Xbrane’s patented high-yield platform technology. This platform positions Xbrane as the most cost-effective biosimilar developer and amongst the top tier global developers. 2021-01-07 Xbrane har ytterligare tre biosimilarer i sin pipeline som adresserar en marknad om 100 miljarder SEK i originalprodukternas försäljning. Xbranes huvudkontor ligger i Solna strax utanför Stockholm.

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As Xbranes leading biosimilar Xlucane (ranibizumab (Lucentis®) biosimilar) moves into the pivotal clinical trial, Xbrane is accelerating development of Xcimzane (certoizumab pegol (Cimzia®) biosimilar) and 2021-03-15 December 19, 2018 I Xbrane Biopharma has submitted its first national Clinical Trial Application (CTA) to the Food and Drug Administration (FDA) in the United States for the start of the Xplore trial for Xlucane, Xbrane Biopharma's lead candidate. This application represents a significant milestone as the product enters the pivotal phase III trial that will support the Marketing Authorization 2020-08-21 Xbrane Biopharma announces that Margareta Hagman will take on the position as interim CFO from September 30, 2020 until a new CFO is in place. Hagman will be part of the management team during the time as interim CFO. She has an extensive experience as CFO from BioGaia AB and holds board positions in two listed companies. Pipeline Prospector delivers free access to a database of drugs under clinical trials which made headlines done by Xbrane Biopharma Xbrane Biopharma, ett bolag som har legat dött och bortglömt i över 1,5 år, men kommit till liv, speciellt efter ett insiderköp på 1,1 miljoner kr av Saeid Esmaeilzadeh, svenska näringslivets Zlatan. Saeid Esmaeilzadeh är styrelseordförande i Xbrane. Xbrane has expanded in recent years and advanced its biosimilar candidate Xlucane (Lucentis biosimilar) into phase III and entered into strategic partnerships with STADA, and Bausch + Lomb. In addition, Xbrane has three additional pre-clinical biosimilar candidates under development that address total originator sales of just under SEK 100 billion.

Xbrane is now in the early process of enrolling patients to the major 580-patient phase The launch of Spherotide in Iran was a milestone for Xbrane, as it proved that the company was able to successfully commercialise a pipeline product. Xbrane generated SEK 21m of sales in 2017, and we estimate 2018 sales of SEK 30m owing to increased market penetration of Spherotide.

Xbrane’s core pipeline, with the lead asset and Lucentis biosimilar Xlucane, is focused on the so called third wave of biosimilars, that is versions of the more complex mAbs or antibody fragment multi-billion blockbuster drugs coming off patent after

Xbrane’s leading product Xlucane, a Lucentis® biosimilar candidate, addresses the SEK 106 billions ophthalmic VEGFa inhibitor market. Xlucane is in phase III and marketing authorization is expected mid-2022. Xbrane has additionally three biosimilars in its pipeline targeting SEK 100 billions in originator sales.

11 Jan 2021 Xbrane has additionally four biosimilars in its pipeline targeting €8.7b in originator sales. Xbrane's head office is in Solna, just outside Stockholm.

Xbrane’s leading product Xlucane, a Lucentis® biosimilar candidate, addresses the €10.4b ophthalmic VEGFa inhibitor market. Xlucane is in phase III and launch is expected mid-2022.

Accessed February 19, 2019. 49. Kashiv Pharma acquires Adello Biologics and becomes Kashiv BioSciences.
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– Martin Åmark, vd Xbrane Biopharm Er pipeline av biosimilarer ( Xlucane, Xcimzane och Xoncane ) baseras på er patenterade teknologiplattform som ni menar är 12 gånger mer effektiv jämfört med standardteknologierna på marknaden. Xbrane Biopharma kliver in på First North Noteringsaktuella Xbrane Biopharma, som tillverkar komplexa kopior, även kallat generika, på befintliga läkemedel vars patent har löpt ut, noteras i dag på Stockholmsbörsens tillväxtlista First North. Xbrane’s leading product Xlucane, a Lucentis® biosimilar candidate, addresses the SEK 106 billions ophthalmic VEGFa inhibitor market.

Xbrane has additionally three biosimilars in its pipeline targeting SEK 100 billions in originator sales. Xbrane’s specific advantage is that its bacterial fermentation system is highly efficient, (up to eightfold higher yields claimed), at producing smaller, biological drugs such as antibody fragments like Xlucane (the lead product) or certolizumab (a pipeline project), or simple enzymes such as pegaspargase (a pipeline project).
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Bad Vilbel, July 12, 2018 – Xbrane Biopharma AB (“Xbrane”) and STADA Arzneimittel AG (“STADA”) have entered into a co-development agreement for Xlucane, a Lucentis ® (ranibizumab) biosimilar. About the agreement The collaboration between Xbrane and STADA is based on a co-development agreement, meaning that the companies will equally contribute to development expenses and share

Xbrane further states that it will initially fund the development of its biosimilar pipeline using resources freed up from Xlucane development, but notes that long-term successful development will require it to raise sufficient capital in the market. Xbrane’s specific advantage is that its bacterial fermentation system is highly efficient, (up to eightfold higher yields claimed), at producing smaller, biological drugs such as antibody fragments like Xlucane (the lead product) or certolizumab (a pipeline project), or simple enzymes such as pegaspargase (a pipeline project). With plans to obtain EU and US marketing authorizations for its Xlucane ranibizumab biosimilar, Xbrane has renegotiated a pre-existing intellectual property licensing agreement with Vaxiion Therapeutics, including the payment of royalties through February 2024.