DGAP-News: Biom'up / Key word(s): Financing
Biom'up issues a new tranche of EUR 5 million from the credit line granted by Athyrium
Saint-Priest, France, August 7, 2019, 6:00 PM (CET) - Biom'up (the "Company"), a specialist in surgical hemostasis, today announces the issuance of a third tranche of its bond financing for EUR 5 million.
This issue was carried out as part of the bond financing subscribed by Athyrium Opportunities III Acquisition LP, a fund managed by Athyrium Capital Management, LP ("Athyrium") for an aggregate amount of up to EUR 35 million, with EUR 25 million issued on March 29, 2018 and EUR 3 million issued on December 31, 2018. The Company can call the EUR 2 million still available under the facility until December 31, 2019, subject to Athyrium waiving existing conditions in light of the Company's financial situation.
This new financing provides the Company with additional resources to support the commercialization of HEMOBLASTTM Bellows and general corporate purposes, allowing to postpone the cash shortfall to early November 2019, previously estimated on September 2019. The Company will continue to need significant financial resources to cover its planned operating and investing activities and is actively looking at all available options.
The bond subscription agreement of March 29, 2018 between Biom'up and Athyrium Capital Management, LP, as amended on August 6, 2019, provides as follows:
Following this transaction, Athyrium, which currently holds 8.57% of the Company's share capital and voting rights on a non-diluted basis, holds a total of 1,201,000 warrants giving the right, upon exercise, to as many new shares of the Company, representing a total holding of 14.68% of the Company's capital and voting rights on a diluted basis.
The bond issue is not made in the context of a public offering (offre au public) of financial instruments in France within the meaning of Article L. 411-1 of the French monetary and financial code (code monétaire et financier) and therefore no prospectus has been submitted for approval (visa) to the Autorité des marchés financiers.
Founded in 2005 and based in the Lyon suburb of Saint-Priest (France), Biom'up develops and commercializes hemostatic products based on patented biopolymers designed to simplify the surgeons' practices for open and minimally invasive surgical procedures, including laparoscopic, in multiple specialties such as cardiac, general, and orthopedic surgery. The Company's lead product, HEMOBLASTTM Bellows and its laparoscopic applicator are marketed in Europe and the United States.
Since its creation, Biom'up has benefited from the support of prominent European and U.S. investors. The Company's shareholders include Bpifrance (including its Innobio fund), Gimv, Lundbeckfond, Athyrium Capital, Financière Arbevel and Invesco, as well as all the Company's management team. Biom'up successfully completed its IPO on Euronext Paris, raising EUR 42.5 million in October 2017.
Since then, the Company carried out a EUR 16 million capital increase in February 2018 and a EUR 7.7 million capital increase by means of a private placement in December 2018. It also entered into a EUR 25 million bond financing agreement with Athyrium, a U.S. fund specializing in innovative companies in the healthcare sector, in March 2018, that was brought to EUR 28 million in December 2018.
HEMOBLAST Bellows is a hemostatic product to control bleeding in a broad range of open and minimally invasive surgical procedures including laparoscopy for multiple specialties such as cardiac, general, and orthopedic surgery.
Uncontrolled bleeding is a major surgical complication associated with higher mortality, longer hospitalization and higher rates of transfusions and reoperations. Beyond its impact on patient's health, this major complication causes excess costs in all surgical specialties and is a burden for hospital budgets across the globe. HEMOBLAST Bellows is the only surgical hemostatic agent approved by the FDA based on the validated SPOT GRADE(TM) Surface Bleeding Severity Scale (SBSS), which demonstrates the ability to control a range of bleeding from minimal (oozing), mild (pooling) and moderate (flowing) bleeding. HEMOBLAST Bellows is proven to control bleeding with flow rates up to 117 mL per minute. Due to its efficacy, versatility and ease of use, HEMOBLAST Bellows is quickly becoming a popular choice amongst U.S. surgeons looking for new options to control surgical bleeding challenges.
Biom'up obtained CE Marking for HEMOBLAST Bellows in December 2016. On the basis of compelling preliminary results (93% effectiveness at 6 minutes, compared with 74% for the control arm) in a major clinical trial, FDA approval for HEMOBLAST Bellows was obtained in December 2017, seven months ahead of the original plan. This allowed for the commercial roll-out of its lead product in the U.S. in the summer of 2018.
In July 2018, Biom'up additionally obtained CE Marking for its HEMOBLAST Bellows Laparoscopic Applicator designed to deliver the HEMOBLAST Bellows powder in all minimally-invasive procedures. In January 2019, the Company obtained the respective approval for HEMOBLAST Bellows Laparoscopic Applicator in the U.S. This has opened up new market segments, representing approximately 500,000 and 443,000 surgeries per year in Europe and the US respectively.
Currently the Company is working to expand the range of applications for HEMOBLAST Bellows. In addition, the approval from the Australian health authorities for the Company's lead product is expected during the second half of 2019.
This document and the information contained herein do not constitute an offer to sell or purchase, or the solicitation of an offer to sell or purchase, securities of Company.
No disclosures or other any information relating to the issue of Company's shares may be distributed to the public in any jurisdiction where a registration or approval is required. No formalities have been or will be undertaken in any jurisdiction outside France where such measures would be required. The offering or subscription of the shares may be subject to specific legal or regulatory restrictions in certain jurisdictions. The Company assumes no liability for any infringement of such restrictions by any person.
This document does not constitute and shall not be construed as constituting a public offer or offer to purchase nor a solicitation to the public in connection with a public offering. The distribution of this document may in certain countries be governed by specific regulations. Any persons in possession of this document should seek advice on and comply with any local restrictions.
This announcement is an advertisement and does not constitute a prospectus within the meaning of Prospectus Regulation (as defined below).
No action has been taken or will be taken to make an offer to the public of the securities requiring a publication of a prospectus in one of the Member States of the European Economic Area. As a result, the securities of the Company may not and will not be offered in any Member State other than France, except in accordance with the exemptions set forth in Article 3 of the Prospectus Regulation.
For the purposes of this provision, an "offer to the public" in relation to the new or existing shares of the Company in any Member State means the communication in any form and by any means of sufficient information on the terms of the offer and the securities to be offered so as to enable an investor to decide to purchase or subscribe for the securities. "Prospectus Regulation" herein refers to the Regulation (EU) 2017/1129 (as amended).
This document may not be distributed, directly or indirectly in the United States of America. This document is not an offer of securities for sale nor the solicitation of an offer to purchase securities in the United States of America or any other jurisdiction where such offer may be restricted. The securities of the Company may not be offered or sold in the United States of America absent registration or an exemption from registration under the US Securities Act of 1933, as amended ("US Securities Act"). The securities of the Company have not been and will not be registered under the U.S. Securities Act and the Company does not intend to make a public offer of its securities in the United States of America.
In the United Kingdom, distribution of this document (referring to any form of communications) is subject to restrictions provided for by article 21 (restrictions relating to "financial promotion" of the Financial Services and Markets Act 2000 ("FSMA"). This document is distributed to, and is directed only at persons who are (i) investment professionals under Article 19(5) of the FSMA (Financial Promotion Order) 2005 (the "Order") as amended, (ii) persons falling within Article 49(2)(a) to (d) of the Order and (iii) any person to which this document may be legally transmitted (all persons mentioned in (i), (ii) and (iii) together being referred to as "Relevant Persons". This document must not be acted on or relied on in the United Kingdom by persons who are not Relevant Persons. Any investment to which this document relates may be proposed to or engaged in the United Kingdom only with Relevant Persons. By receiving this document, you must notify the Company that you are among the categories of persons mentioned above. Such conditions are set out in section 184.108.40.206 of the Company's French language « document de référence » for the year 2018 available on the Company's website: www.biomup.com and upon written request from the Company at 8 allée Irène Joliot-Curie, 69800 Saint-Priest.
|8, allée Irène Joliot Curie|
|Phone:||+33 (0)4 86 57 36 10|
|Fax:||+33 (0)4 37 69 00 84|
|Listed:||Regulated Unofficial Market in Berlin; London, Paris|
|EQS News ID:||853527|
|End of News||DGAP News Service|