BioInvent Financial Statement January 1 - December 31, 2018

BioInvent Financial Statement January 1 - December 31, 2018

PR Newswire

LUND, Sweden, Feb. 25, 2019

LUND, Sweden, Feb. 25, 2019 /PRNewswire/ --

Fourth quarter 2018, October – December

Full year report 2018, January - December

Important events in the fourth quarter and after the reporting period

Comments from the CEO

Martin Welschof, CEO of BioInvent, says "We are pleased to have secured the financing announced today since it provides us with the opportunity to accelerate our drug development pipeline. Clinical results will drive the value of our pipeline. The financing consists of a fully underwritten rights issue of SEK 210 million and a directed issue of SEK 30 million at equal terms, and in addition an over-allotment option for up to SEK 70 million, that can be exercised if the rights issue is over-subscribed.

We intend to use the net proceeds to mainly expand the clinical development of BI-1206 for treatment of hematological cancers, which is currently in a Phase l/lla study with topline results expected in H1 2020, as well as advancing three compounds into the clinic in solid cancer indications. These are an anti FcγRllB antibody in combination with an anti-PD1 antibody, BI-1607 in combination with a check point inhibitor, BI-1808 as a single agent and in combination with an anti-PD1 antibody. The funds will also be used to continue development of the Company's prioritized preclinical projects, including the collaboration with Transgene.

If the over-allotment option is utilized in full, the net proceeds hereof is intended to be used towards the activities described above and is estimated to take the anti-FcγRllB antibody in combination with an anti-PD1 antibody to topline results by H2 2020.

The financing followed a few months of strong progress for BioInvent. Last month, we received orphan designation from the FDA for BI-1206 in mantle cell lymphoma, and we are looking forward to generating data from our Phase I/IIa trial to support the use of BI-1206 in combination with rituximab in this indication.

Also, we presented two back-to-back posters at the annual meeting of the Society for Immunotherapy of Cancer (SITC) together with Transgene, featuring positive data supporting our ongoing collaboration to develop a novel oncolytic virus encoding for an anti-CTLA-4 antibody. We published data in the leading cancer journal Immunity on the cellular and molecular mechanism-of-action of antibodies to the co-stimulatory immune checkpoint receptor 4-1BB; and lastly we presented our discovery platform F.I.R.S.T.™ at the Society for Laboratory Automation and Screening (SLAS) 2019 in Washington, D.C..

In addition, we signed a manufacturing agreement with an undisclosed U.S. cell therapy company for the production of cGMP compliant material to support their clinical development programs, which is expected to generate revenue of approximately USD 1.5 million, mainly in 2019.

With financing in place, we will continue to focus on opportunities to partner our product candidates. We look forward to the opportunity to deliver medical solutions to meet patient needs and value to our shareholders."

Contact 

Any questions regarding this report will be answered by Martin Welschof, CEO, +46(0)46-286-85-50, martin.welschof@bioinvent.com. The report is also available at www.bioinvent.com.

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The following files are available for download:

https://mb.cision.com/Main/583/2748563/997027.pdf

BioInvent Financial Statement January 1 â€" December 31, 2018 (PDF)

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