What's new?
04/04/2018

• Sofinnova Crossover 1 est le plus grand fonds crossover dédié à la santé en Europe.
• Avec ce nouveau fonds, Sofinnova Partners poursuit activement sa stratégie visant à élargir sa plateforme d’investissements en sciences de la vie sur l’ensemble de la chaîne de valeur, de l’amorçage aux sociétés de croissance.
• Bpifrance* et CNP Assurances sont co-sponsors du fonds.

Paris, France – 4 avril 2018 — Sofinnova Partners, un leader du capital-risque en Europe spécialisé dans les sciences de la vie, annonce le lancement de son premier fonds crossover dédié à la santé en Europe, d’un montant de 275 millions d’euros (340 millions de dollars), au-delà de l’objectif du premier closing à 250 millions d’euros. Avec ce nouveau fonds, Sofinnova Partners franchit une étape supplémentaire dans le déploiement de son projet de croissance visant à étendre son champ d’intervention dans les différents segments de l’investissement dans les sciences de la vie, grâce à des équipes dédiées.

Dans la continuité de la stratégie appliquée avec succès depuis plusieurs décennies avec ses fonds Capital intervenant en early-stage, Sofinnova Crossover I investira dans la biopharmacie et l’instrumentation médicale. Il ciblera en priorité des technologies de rupture permettant des innovations thérapeutiques portées par des équipes managériales expérimentées. Sofinnova Partners investira comme chef de fil ou investisseur de référence dans une quinzaine d’entreprises privées ou cotées. Environ 80% du fonds seront investis en Europe, et les 20% restants ailleurs, principalement en Amérique du Nord. Une équipe de quatre associés très expérimentés investira le fonds, en s’appuyant sur l’expérience élargie de Sofinnova Partners, son track record et son organisation. Ce nouveau fonds a su attirer la confiance d’investisseurs internationaux de premier plan, notamment des fonds souverains, compagnies d’assurance, corporate, et family offices. La majorité des fonds levés viennent d’Europe, en particulier de France, d’Italie, du Danemark, d’Irlande et de Suisse, mais aussi d’Asie avec des investisseurs originaires de Chine et de Singapour. En plus de BPIfrance* et de CNP Assurances, une société pharmaceutique chinoise de premier plan, le fonds public d’investissement danois, et des family offices tels que Fidim et KCK représentant de grandes familles industrielles d’Europe et d’Asie figurent parmi les investisseurs du nouveau fonds.

Antoine Papiernik, Président de Sofinnova Partners, déclare : “Avec le lancement de l’activité crossover, Sofinnova Partners construit sur son track record unique en early-stage. Beaucoup des entreprises que nous avons financées dès leur démarrage sont devenues au cours des années de grandes entreprises, certaines valorisées plusieurs milliards d’euros ; nous avons ainsi acquis une expérience unique sur la façon de les accompagner au stade d’après. Ce fonds complète notre plateforme d’investissement dans les sciences de la vie, nous permettant d’être actifs tout au long de la chaîne de valeur depuis l’investissement d’amorçage jusqu’aux phases plus avancées.”

Jacques Theurillat, Partner dans l’équipe crossover de Sofinnova Partners, poursuit : “Le marché européen de la santé est devenu mature avec des centaines d’entreprises privées et cotées à la recherche de fonds pour financer leur croissance, et Sofinnova Partners, avec son image de marque, son track record, et son expérience, est idéalement positionnée pour identifier les meilleures opportunités en Europe et accompagner leur transformation en leaders internationaux.”

Sur ce fonds Sofinnova Crossover I, Triago a agi en tant qu’agent de placement et Clifford Chance Europe LLP en tant que conseil juridique.

*Bpifrance intervient pour son compte propre et pour le compte du SGPI dans le cadre du Programme d’investissements d’Avenir (PIA)

Contact presse pour SOFINNOVA PARTNERS
Anne REIN Tel: +33 (0)6 03 35 92 05 @: anne.rein@strategiesimage.com

A propos de Sofinnova Partners
Sofinnova Partners est un des leaders du capital risque en Europe spécialisé dans les sciences de la vie. Basée à Paris, l’équipe est composée de professionnels issus d’Europe, des Etats Unis et de Chine. La société investit dans les technologies de changement de paradigme aux côtés d’entrepreneurs visionnaires. Sofinnova Partners intervient en priorité dans les start up et spin-off d’entreprises en tant qu’investisseur fondateur et chef de file. Depuis 45 ans, la société a accompagné plus de 500 entreprises à travers le monde devenues des leaders sur leur marché. Sofinnova Partners gère aujourd’hui 1,9 milliard d’euros.

24/09/2013

London, September 24th 2013. Synthace, the applied synthetic biology company developing high value chemical and biological products, announces that it has closed a funding round raising £1.3 Million. Sofinnova Partners’ Green Seed Fund led the financing, joined by a syndicate of angel investors.
Synthace is applying its world leading platform of technologies to rapidly engineer and optimise novel biological systems for the production of specialty chemicals and biological products. Synthace bioengineering is enabled by a tight integration of computational modelling and big data analysis with wet lab experimental design and novel molecular biology tools. The company’s platform is broadly applicable across multiple industry sectors, including chemicals, healthcare, energy and agriculture, and has the potential to create as yet uncharted markets and opportunities.
Tim Fell, CEO of Synthace, commented: « We are delighted to have attracted Sofinnova Partners’ Green Seed Fund and see this funding as a very strong validation of our company, technology and commercial focus. It will allow us to demonstrate production of our first chemical products at scale, prior to forming partnerships within the chemicals industry to take them to market.”
Joško Bobanović, Partner at Sofinnova Partners responsible for the fund, added: « Synthace offers a unique combination of a revolutionary technical platform, entrepreneurial and visionary team, developing advanced products for extremely large markets. Green Seed Fund focuses on European investments in renewable chemistry and has recognised Synthace as one of the leaders in this sector offering, in a way, version 2.0 of synthetic biology application.”

For further details, please contact:
Tim Fell, CEO Synthace Tel: + 44 (0) 20 3642 1350

Notes to Editors:
Synthace is the UK’s first dedicated synthetic biology company with a world leading platform of technologies for the rapid engineering and optimisation of novel biological production systems. A spin out of University College London, Synthace harnesses the ability of micro-organisms to produce complex, high-value chemical and biological products from sustainable and renewable feedstocks. In addition to equity funding, the company has received a £500,000 Technology Strategy Board award entitled ‘Rapid Engineering of Cellular Factories’, in collaboration with University College London and University of Manchester. While Synthace bioengineering is broadly applicable across multiple industry sectors, the company is initially focused towards applications in the production of specialty chemicals.
More information is available at www.www.synthace.com
Sofinnova Partners is an independent venture capital firm based in Paris, France. For more than 40 years, the firm has backed nearly 500 companies at different stages of their development – pure creations, spin-offs, as well as turnaround situations – and worked alongside Europe’s key entrepreneurs in the Life Sciences industry. With €1.3 billion of funds under management, Sofinnova Partners has created market leaders with its experienced team and hands-on approach in building portfolio companies through to exit. sofinnova.social-unit.fr

29/08/2013

Paris, France, 29 août 2013. Sofinnova Partners, société de capital-risque basée à Paris, a mené le financement de Série A qui a permis à ObsEva SA, une société biopharmaceutique basée en Suisse et spécialisée en médecine de la reproduction féminine, de lever 32M CHF (25,6M EUR). Pour ce premier tour de financement, Sofinnova Partners a été rejoint par deux co-investisseurs, Sofinnova Ventures et Novo A/S.

ObsEva est spécialisée dans le traitement de la menace d’accouchement prématuré. La société a été cofondée en novembre 2012 par Ernest Loumaye, MD, PhD, un serial entrepreneur que Sofinnova Partners a déjà accompagné avec succès dans PregLem, une société spécialisée en médecine de la reproductionet plus particulièrement le traitement du fibrome utérin. PregLem a été acquise en 2010 par Gedeon Richter pour 445M CHF (361M EUR). L’équipe dirigeante d’ObsEva est pilotée par ses deux co-fondateurs, Ernest Loumaye, Directeur Général, et André Chollet, PhD, Directeur Scientifique.

Simultanément à l’opération de financement, ObsEva a signé un accord de licence mondial avec Merck Serono pour développer et commercialiser certains de leurs produits dans le domaine de l’obstétrique. Dans le cadre de cet accord, Merck Serono a acquis une participation minoritaire au capitald’ObsEva. Le financement va permettre d’accélérer le développement de ces produits qui ont le potentiel d’être des « best-in-class ». En combinant un rationnel biologique solide à un profil pharmaceutique différenciant, ObsEva est ainsi parfaitement positionné pour développer une nouvelle classe de médicaments capables d’apporter aux patientes des solutions de rupture dans la menace d’accouchement prématuré, un domaine médical où il existe un important besoin clinique à combler.

Rafaèle Tordjman, MD, PhD, Partenaire Associée chez Sofinnova Partners, déclare : « Au fil des ans, nous avons développé des liens solides avec Ernest Loumaye. Dans la continuité du succès de PregLem, Sofinnova Partners a financé l’amorçage d’ObsEva. Nous sommes ravis de continuer à soutenir une équipe d’une telle qualité et favoriser le développement d’une nouvelle génération de thérapies pour traiter la menace d’accouchement prématuré ». Ernest Loumaye, PDG, poursuit : « ObsEva répond à des besoins essentiels aujourd’hui encore insatisfaits car les thérapies existantes pour traiter la menace d’accouchement prématuré demeurent limitées en termes d’efficacité ou de sécurité. Aujourd’hui, nous estimons que le coût lié à la menace d’accouchement prématuré est autour de 27 milliards de dollars par an aux Etats Unis. Les produits que nous développons devraient permettre d’améliorer radicalement les options thérapeutiques proposées à des millions de femmes ».

A propos de Sofinnova Partners
Sofinnova Partners est une société de capital-risque indépendante basée à Paris. Depuis plus de 40 ans, la société a financé près de 500 sociétés – start-up, spin-off et opérations de retournement. Elle a accompagné les plus grands entrepreneurs européens dans le domaine des sciences de la vie. Avec 1,3 milliard d’euros sous gestion, l’équipe de Sofinnova Partners, reconnue pour sa capacité à aider et à soutenir les entreprises de son portefeuille de la création à la sortie, a permis l’émergence de leaders sur leurs marchés. sofinnova.social-unit.fr

A propos d’ObsEva SA
ObsEva est une société biopharmaceutique basée en Suisse spécialisée dans le développement des traitements innovants dans le domaine de la reproduction féminine. ObsEva s’intéresse particulièrement au traitement de la menace d’accouchement prématuré. ObsEva a été créée en 2012 par Ernest Loumaye MD, PhD et André Chollet PhD. Ernest Loumaye est un spécialiste de la médecine reproductrice féminine avec une expérience de plus de 20 ans dans l’industrie biopharmaceutique. Il a précédemment co-fondé et dirigé PregLem. André Chollet est un spécialiste de la chimie médicale et pharmaceutique, fort d’une expérience de plus de 30 ans dans le secteur, notamment chez Biogen, GSK et Merck Serono. www.obseva.com

29/07/2013

Zürich-Schlieren, Switzerland, July 29, 2013 – Following recently signed collaborations with GlaxoSmithKline Biologicals (GSK) and Janssen Pharmaceuticals (JPI), GlycoVaxyn AG, a leader in the development of innovative conjugate vaccines, today announced that it has secured a Strategic Translation Award from the Wellcome Trust to finance its Shigella program.

The award will allow the Company to advance its Shigella bioconjugate vaccine by funding human safety and challenge studies in healthy adults to confirm the efficacy of a monovalent Shigella flexneri 2a vaccine, before testing a multivalent vaccine in field studies in children. Clinical trials are scheduled to start in 2014 in the USA.
Shigella is one of the main causes of a diarrheal disease that causes illness and death among young children in low-income countries. Various serotypes of this Gram-negative bacterium are responsible for the diarrhea and, with regional differences in serotype distribution, up to 6 serotypes need to be included in a vaccine to provide broad protection and prevent Shigellosis worldwide.
GlycoVaxyn’s in vivo glycosylation technology enables the possibility to develop such a complex multivalent Shigella vaccine for the first time. Complexes of the antigenic surface polysaccharides and proteins can now be directly synthesized in genetically engineered bacterial cells. This multivalent Shigella bioconjugate vaccine can be manufactured at low costs, a distinct advantage compared to conjugate vaccines that are chemically produced.
“An estimated 1.1 million people die from Shigella infections each year, mostly children under the age of five living in low income countries,” said Richard Seabrook, Ph.D., head of Business Development at the Wellcome Trust. “With rising antibiotic resistance limiting our treatment options, we urgently need an affordable vaccine that will provide broad protection against the many strains of Shigella bacteria that cause disease.”
Dr Michael Wacker, chief scientific officer of GlycoVaxyn added, “We are very honored to work with this prestigious global charitable foundation and proud to contribute to the development of a vaccine that addresses a critical medical need among millions around the world. GlycoVaxyn has previously conducted a Phase 1 study in healthy volunteers on a single serotype Shigella conjugate vaccine. This collaboration will enable us to investigate a new vaccine against a different single serotype, moving this important program forward towards a broad acting vaccine that protects against multiple serotypes.”
Gordon Dougan, Ph.D., member of GlycoVaxyn’s Scientific Advisory Board and professor at the Wellcome Trust Sanger Institute in Cambridge commented, “GlycoVaxyn is using highly innovative technology to break open new fields in vaccinology. I am delighted to see them work together with the Wellcome Trust to apply this technology to vaccines for children suffering from dysentery”.

About GlycoVaxyn AG
GlycoVaxyn is a privately-funded company developing a portfolio of novel bio-conjugate vaccines against common severe bacterial infections produced with its unique, proprietary in vivo glycosylation platform. With this platform, the company can develop and produce immunogenic glycoprotein conjugates in a biological process that circumvents many of the challenges and uncertainties involved in currently used chemical methods. Besides Shigella, the portfolio includes preclinical programs targeting major infectious diseases such as Staphylococcus aureus and Streptococcus pneumoniae. GlycoVaxyn is funded by a top-tier group of private investors including Sofinnova Partners, Index Ventures and Edmond de Rothschild Investment Partners and recently entered collaborations with GSK and JPI. For further information, visit www.glycovaxyn.com.

About The Wellcome Trust
The Wellcome Trust is a global charitable foundation dedicated to achieving extraordinary improvements in human and animal health. It supports the brightest minds in biomedical research and the medical humanities. The Trust’s breadth of support includes public engagement, education and the application of research to improve health. It is independent of both political and commercial interests. www.wellcome.ac.uk

Contacts:
Robert Flamm
GlycoVaxyn AG Russo Partners, LLC
Tel: +41-44-733-8595 Tel: +1-212-845-4226
media@glycovaxyn.com robert.flamm@russopartnersllc.com

01/06/2013

Including NDA-Ready Novel Dyslipidemia Treatment to Complement Cardiovascular Portfolio

AstraZeneca today announced that it has entered into a definitive agreement to acquire Omthera Pharmaceuticals, a specialty pharmaceutical company based in Princeton, New Jersey, focused on the development and commercialisation of new therapies for abnormal levels of lipids in the blood, referred to as dyslipidemia.

Omthera’s investigational product, EpanovaTM, for the potential treatment of patients with very high triglycerides, is a novel omega-3 free fatty acid composition that has been shown to bolster levels of eicosapentaenoic acid and docosahexaenoic acid significantly in the blood. In studies to date, it has been shown to reduce triglyceride levels and improve other key lipid parameters and is expected to increase convenience for patients by providing both two and four gram once-a-day doses with or without meals.

Under the terms of the agreement, AstraZeneca will acquire Omthera for $12.70 per share, or approximately $323 million, which has an Enterprise Value of approximately $260 million after incorporating Omthera’s cash balances of approximately $63 million. This represents a premium of 88% on Omthera’s closing price on Friday 24 May 2013. In addition to the cash payment, each Omthera shareholder will receive Contingent Value Rights (CVRs) of up to approximately $4.70 per share, equating to approximately $120 million in total, if specified milestones related to Epanova are achieved, or if a milestone related to global net sales is achieved. This will bring the total potential acquisition cost to approximately $443 million.

Omthera has completed pharmacokinetic and Phase III clinical studies to investigate the safety and efficacy profile of Epanova, a coated soft gelatin capsule containing a complex mixture of polyunsaturated free fatty acids derived from fish oils. In 2012, Omthera reported positive results from two Phase III trials (EVOLVE and ESPRIT) examining the effectiveness of Epanova in lowering very high triglycerides, and in reducing non-HDL cholesterol in combination with a statin for patients with high triglycerides. Both trials were conducted under a Special Protocol Assessment with the US Food and Drug Administration.

Omthera is expected to file a new drug application (NDA) in the US for Epanova in mid-2013 for patients with severe hypertriglyceridemia (triglyceride levels greater than or equal to 500mg/dL), with regulatory filings in other markets to follow. AstraZeneca aims to file a supplemental NDA as soon as possible for Epanova as a treatment for patients with mixed dyslipidemia (triglyceride levels of 200-499mg/dl), as well as in a fixed dose combination with CRESTOR (rosuvastatin calcium) for those mixed dyslipidemia patients at high risk of a cardiovascular event. AstraZeneca intends to pursue a large-scale cardiovascular outcomes trial for Epanova in combination with statins.

Pascal Soriot, Chief Executive Officer of AstraZeneca said: “The number of people with elevated triglyceride levels is rising rapidly across the world, due in part to the increasing prevalence of obesity and diabetes. There is a clear need for effective and convenient alternatives to some of the existing treatments. Epanova offers real potential both as a distinctive monotherapy for the treatment of hypertriglyceridemia and in combination with Crestor for patients at high risk of  adverse cardiovascular events. This is an exciting acquisition that clearly complements our existing portfolio in cardiovascular and metabolic disease, one of our core therapy areas.”

Gerald L. Wisler President amp; CEO, Board Member, and Co-Founder of Omthera, commented: “We are delighted to be joining AstraZeneca, a leading pharmaceutical company with a proven track record in the development and commercialisation of global brands in the area of cardiovascular disease. We believe strongly that AstraZeneca can maximise the value of Epanova not only as a monotherapy treatment for dyslipidemia but also as a treatment for cardiovascular disease in combination with Crestor. »

The Board of Directors of Omthera has unanimously approved the terms of the agreement, and has recommended that its shareholders approve the transaction. AstraZeneca’s Board has also approved the terms of the agreement. Subject to the approval of Omthera’s shareholders as well as other conditions including customary regulatory approvals, the transaction is expected to close in the third quarter of 2013. Omthera’s shareholders representing approximately 60% of the current total shares outstanding have entered into a voting agreement with AstraZeneca to vote in favour of the transaction, subject to the conditions set out in the voting agreement.

About Epanova™Epanova is a patent protected, novel, ultra-pure mixture of the free fatty acid forms of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) that meaningfully reduces triglycerides, improves other key lipid parameters and is expected to increase patient convenience with 2-gram once-a-day dosing with or without meals. Epanova is a coated soft gelatin capsule containing a complex mixture of polyunsaturated free fatty acids derived from fish oils, including multiple long-chain omega-3 and omega-6 fatty acids, with EPA, DHA, and docosapentaenoic acid being the most abundant forms of omega-3 fatty acids. Omthera Pharmaceuticals has completed pharmacokinetic and Phase III clinical studies to investigate the safety and efficacy profile of Epanova. In 2012 Omthera reported positive results from its Phase III EVOLVE and ESPRIT trials, both of which were conducted under a Special Protocol Assessment with the U.S. Food and Drug Administration. Omthera is expected to file an NDA for Epanova in mid-2013 for patients with triglyceride levels greater than or equal to 500mg/dL or for severe hypertriglyceridemia. Other planned indications for the monotherapy are as an adjunct to statin therapy and diet in  patients with mixed dyslipidemia and increased triglycerides  (>200 and

About hypertriglyceridemia Hypertriglyceridemia is a serum lipid disorder (dyslipidemia) defined by serum triglyceride levels of ≥150 mg/dL. It is associated with an increased risk of cardiovascular diseases, such as coronary artery disease, or acute risk of pancreatitis if triglyceride levels exceed 500 mg/dL. In 2011, dyslipidemia affected 352 million people aged 20 or older across the major pharmaceutical markets (United States, France, Germany, Italy, Spain, United Kingdom, and Japan), caused by genetic predisposition and various secondary/contributing factors, such as lifestyle and dietetic behaviour (e.g. obesity, malnutrition, metabolic syndrome), as well as by numerous diseases (e.g. diabetes, renal disease, autoimmune diseases). It is estimated that there are 5 million patients in the U.S. with TG levels > 500 mg/dL. A recent NHANES analysis of dyslipidemia in the US indicated that low-density lipoprotein levels have actually declined since the last analysis, but the percentage of patients with severe hypertriglyceridemia has risen sharply along with the dramatic increases in obesity.

About mixed dyslipidemia The second most common form of dyslipidemia is mixed dyslipidemia. Physicians estimate that between 22% and 37% of patients have this form of dyslipidemia. The term mixed dyslipidemia refers to a condition in which the patient suffers from hypercholesterolemia, low high-density lipoprotein levels and hypertriglyceridemia. Due to the nature of the condition and the fact that different classes of antidyslipidemics offer different benefits in controlling lipid abnormalities, a combination therapy is often considered the most beneficial in patients with mixed dyslipidemia. Options are a combination of a statin with either fibrate or nicotinic acid or Omega-3 fatty acids.

About Omthera Pharmaceuticals, Inc. Founded in 2008, Omthera Pharmaceuticals, Inc. is an emerging specialty pharmaceutical company that listed on NASDAQ in April 2013 (NASDAQ: OMTH). Led by a team of experts with exceptional experience in developing new therapies for lipid disorders, Omthera is dedicated to developing innovative therapies for the millions of patients who have elevated triglyceride levels and increased risk of cardiovascular disease. Omthera currently has 14 employees based in Princeton, New Jersey. For more information please visit: www.omthera.com 

About AstraZeneca AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit: www.astrazeneca.com

 

CONTACTS

Omthera Pharmaceuticals contacts

Chris Schade, Executive Vice President and Chief Financial Officer +1 908 741 6402 (US)

AstraZeneca contacts

Media Enquiries Ayesha Bharmal +44 20 7604 8034 (UK/Global) Vanessa Rhodes +44 20 7604 8037 (UK/Global) Tony Jewell +1 (302) 885 4594 (US) Jacob Lund +46 8 553 260 20 (Sweden)

Investor Enquiries James Ward-Lilley                      +44 20 7604 8122    mob: +44 7785 432613 Karl Hård                                    +44 20 7604 8123  mob: +44 7789 654364 Colleen Proctor                           + 1 302 886 1842     mob: +1 302 357 4882 Ed Seage                                    + 1 302 886 4065     mob: +1 302 373 1361

20/05/2013

Princeton, N.J. and PARIS – May 20, 2013 – STENTYS (FR0010949404 – STNT), a medical technology company commercializing in Europe the world’s first and only Self-Apposing® Stent to treat acute myocardial infarction (AMI), announced today that the first patient was enrolled in APPOSITION V, the pivotal FDA-approved IDE trial which will enable the Company to apply for marketing approval of the Self-Apposing Stent in the United States.
APPOSITION V is a multi-center, randomized, two-arm clinical trial that will enroll up to 880 heart attack (ST-elevation myocardial infarction or STEMI) patients at 50 sites in the U.S. and worldwide. The trial is designed to compare the clinical outcome of patients treated with the STENTYS Self-Apposing Stent with a balloon-expandable stent already approved for this indication, the Abbott Multi-Link stent, at 12 months after the procedure. Principal investigators of the study are Roxana Mehran, M.D., Professor of Medicine and Director of Interventional Cardiovascular Research and Clinical Trials at Mount Sinai School of Medicine (New York), and Maurice Buchbinder, M.D., Professor of Clinical Medicine at Stanford University (Stanford, Calif.).
“The APPOSITION V trial will be a landmark study as it is the first time a novel device, that has already shown impressive clinical results in Europe, will benefit our STEMI patients here in the U.S.” said Dr. Mehran. “We would like to congratulate Dr. Karel Koch from Amsterdam Medical Center for enrolling the first patient in this study.”
“This is a historic milestone for STENTYS, as we begin the U.S. trial that will allow us to file our marketing application with the FDA,” said Gonzague Issenmann, CEO and co-founder of STENTYS. “The STENTYS Self-Apposing Stent has the potential to replace the current gold standard of conventional balloon-expandable stents in the AMI setting.”

About the STENTYS Self-Apposing® Stent
The STENTYS Self-Apposing® Stent addresses the stent-sizing dilemma that cardiologists are confronted with when treating heart attack patients. It fits into the contour of a blood vessel, and its shape and diameter adapt as the vessel dilates and the initial clot dissolves during the post-AMI phase, thus reducing the risk of malapposition and complications associated with conventional stents in this setting. The STENTYS Self-Apposing Stent has been marketed in Europe since receiving CE Mark in 2010.

About the APPOSITION V Study
APPOSITION V is an interventional, multi-center, randomized, two-arm clinical trial to evaluate the safety and effectiveness of the STENTYS Self-Apposing® Stent in the treatment of de novo stenotic lesions in coronary arteries in 880 patients undergoing primary revascularization due to ST-elevation myocardial infarction (STEMI) as compared to the Multi-Link coronary system (Abbott Vascular, Inc.). The trial’s primary endpoint is target vessel failure (TVF), which is defined as a composite of cardiac death, target vessel recurrent myocardial infarction or clinically driven target vessel revascularization (TVR), at 12 months post-procedure. The powered secondary endpoint is acute stent malapposition and will be assessed by intravascular ultrasound (IVUS) on the first 225 patients. All patients will undergo clinical follow up at 30 days, six months, nine months and 12 months, with an annual checkup through three years. Fifty sites are expected to participate in the U.S. and worldwide. More information can be found at www.clinicaltrials.gov.

About STENTYS
STENTYS is developing and commercializing innovative solutions for the treatment of patients with acute myocardial infarction (AMI, or heart attack) and complex coronary artery disease. STENTYS’ Self-Apposing® Stents are designed to adapt to vessels with ambiguous or fluctuating diameters, particularly in the post-infarction phase, in order to prevent the malapposition problems associated with conventional stents. In the APPOSITION III clinical trial, STENTYS stents demonstrated a very low one-year mortality rate among 1,000 high-risk AMI patients when compared to recent studies with conventional stents. More information is available at www.stentys.com.

This press release contains forward looking statements about the Company’s business. Such forward looking statements are based on numerous assumptions regarding the Company’s present and future business strategies and the environment in which it will operate in the future which may not be accurate. Such forward-looking statements involve known and unknown risks which may cause the Company’s actual results, performance or achievements to differ materially from any future results, performance or achievements expressed or implied by such forward-looking statements. Such factors include, among others, risks associated with the development and commercialization of the Company’s products, market acceptance of the Company’s products, its ability to manage growth, the competitive environment in relation to its business area and markets, its ability to enforce and protect its patents and proprietary rights, uncertainties related to the U.S. FDA approval process, including with respect to a pre-market approval for the Company’s BMS, slower than expected rates of patient recruitment for clinical trials, the outcome of clinical trials, and other factors, including those described in the Section 4 “Risk Factors” of the Company’s 2011 Registration Document (document de référence) filed with the Autorité des marchés financiers in France on June 25, 2012 under number R.12-033 as such section may be updated from time to time.

STENTYS
Stanislas Piot, CFO
Tel.: +33 (0)1 44 53 99 42
stan.p@stentys.com
STENTYS is listed on Comp. C of the NYSE Euronext Paris
ISIN: FR0010949404 – Ticker: STNT
Europe: NewCap.
Dusan Oresansky / Pierre Laurent
Tel.: +33 (0)1 44 71 94 93
stentys@newcap.fr
US: MacDougall Biomedical Communications
Charles Liles, Tel.: 781 235 3060
Christine Labaree, Tel.: 650 339 7533
stentys@macbiocom.com

14/05/2013

Minneapolis, MN, May 14, 2013 – BioAmber Inc. (“BioAmber”) (NYSE: BIOA.U), announced today the closing of its initial public offering of 8,000,000 units consisting of one share of common stock and one warrant to purchase half of one share of common stock at $10.00 per unit, before underwriting discounts and commissions. Each warrant will be exercisable at an exercise price of $11.00 per whole share of common stock. All units are being sold by BioAmber. The units are listed on the New York Stock Exchange (“NYSE”) under the symbol “BIOA.U”. The common stock and warrants comprising the units will begin trading separately on NYSE under the symbols “BIOA” and “BIOA.WS”, respectively, on Monday, June 10, 2013 at which time trading of the units will be suspended and the units will be delisted. BioAmber also intends to list its common stock on the Professional Segment of the regulated market of NYSE Euronext in Paris under the symbol “BIOA.”

Credit Suisse, Barclays and Société Générale are acting as joint book-running managers for the offering. Pacific Crest Securities is acting as co-manager for the offering.

A registration statement relating to these securities has been filed with, and declared effective by, the U.S. Securities and Exchange Commission on May 9, 2013. This press release shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

The offering of these securities was made only by means of a prospectus, copies of which may be obtained from Credit Suisse Securities (USA) LLC by mail at One Madison Avenue, New York, New York 10010, Attention: Prospectus Department, or by calling toll free (800) 221-1037, or by emailing newyork.prospectus@credit-suisse.com.

About BioAmber Inc.
BioAmber is a next generation chemicals company. Its proprietary technology platform combines industrial biotechnology and chemical catalysis to convert renewable feedstocks into chemicals including succinic acid and 1,4-butanediol, which are used in a wide variety of everyday products such as plastics, food additives and personal care products. For more information visit the company’s web site at: www.bio-amber.com.

Forward-Looking Statements
This press release contains forward-looking statements, which are subject to substantial risks, uncertainties and assumptions. These statements often include words such as “believe,” “expect,” “anticipate,” “intend,” “plan,” “estimate,” “seek,” “will,” “may” or similar expressions. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee that the events and circumstances reflected in the forward-looking statements will be achieved or occur and the timing of events and circumstances and actual results could differ materially from those projected in the forward- looking statements. Accordingly, you should not place undue reliance on these forward-looking statements. All such statements speak only as of the date made, and we undertake no obligation to update or revise publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

Investor Contact
Chad Rubin
The Trout Group, LLC
New York
740 Broadway
9th Floor
New York, NY 10003
Tel: + 1 (646) 378-2947
Fax: +1 (646) 378-2901
crubin@troutgroup.com

Media Contact
Kathryn Sheridan
Sustainability Consult
ks@sustainabilityconsult.com
Mobile: +32 496 116198

26/04/2013

PRINCETON, N.J. and PARIS – 25 April 2013 – STENTYS (FR0010949404 – STNT), a medical technology company commercializing in Europe the world’s first and only Self-Apposing® stent to treat acute myocardial infarction (AMI), today reports its first quarter revenues to 31 March 2013 and announces the first distributor contracts signed outside of Europe.

  • Change in quarterly revenues

STENTYS recorded a solid first quarter of 2013 with revenues totaling €725.0 thousand, an increase of 47% compared with the same quarter last year. Revenues during the quarter were driven largely by sales of Self-Apposing stents using the new-generation catheter introduced in the third quarter of 2012.

  • Geographic expansion beyond Europe

Backed by experience acquired during the pre-marketing phase of the Self-Apposing stent, STENTYS is pursuing commercial expansion beyond Europe by forming partnerships with local distributors in new high-potential countries where the European CE mark is recognized. STENTYS recently signed agreements with leading regional distributors of cardiovascular products in Saudi Arabia, Jordan, Lebanon and Egypt. The Company estimates that the Middle East market for coronary stenting is about €160 million.

  • Clinical update on recent and ongoing trials

– APPOSITION III clinical trial
Definitive 12-month data from the APPOSITION III clinical trial on 1,000 heart attack patients were presented in early March at the prestigious annual American College of Cardiology conference. The impressive results were covered in the US press and were well received by cardiologists, notably in the United States, the world’s largest stent market. In the study, STENTYS’ stent showed the lowest mortality rate (2.0%) of any major heart attack trial with conventional stents, and the rate of re-infarction was also particularly low (1.3%).
– APPOSITION IV clinical trial
This randomized trial enrolled 150 heart-attack patients treated with either the STENTYS Sirolimus-eluting stent or the Medtronic Resolute® stent, with the objective of comparing long-term stent apposition. The 4-month results should be announced during the second half of 2013.
– APPOSITION V clinical trial
The IDE for the APPOSITION V pivotal study, the last trial in the APPOSITION program, has been approved by the US Food and Drug Administration (FDA). The trial aims to compare the clinical efficacy of the Self-Apposing stent with that of the stent already approved for the AMI indication in the US, the Abbott MultiLink stent. The trial is expected to be launched during the second quarter of 2013 and will enroll approximately 880 patients who will be evaluated 12 months after treatment.
Gonzague Issenmann, Chief Executive Officer and co-founder of STENTYS, concludes: “The solid growth recorded this quarter confirms STENTYS’ steady expansion, in line with the Company’s plan. Growth in the new countries outside Europe is expected to be fueled by the excellent results from the APPOSITION III clinical trial: these results represent the most significant developments since the creation of STENTYS and provide further evidence that the Self-Apposing stent is the optimal solution for treating heart attacks.”

  • Upcoming financial results

STENTYS expects to publish its revenues for H1 2013 on 25 July 2013.

About the APPOSITION III Study
APPOSITION III is a prospective, single-arm, multi-center (50 hospitals across Europe) post-market trial to assess the long term performance of the STENTYS Self-Apposing® stent in routine clinical practice in 1,000 patients suffering from ST-Elevation Myocardial infarction (STEMI). The trial’s primary endpoint is Major Adverse Cardiac Events (MACE) at 12 months. MACE is defined as cardiac death, target vessel re-MI, emergent by-pass, or clinically-driven TVR by percutaneous or surgical methods. The MACE rate at one year was 9.3% for the full study population, where conventional stents average 11.1%. Mortality rate at one year was 2.0%, where conventional stents average 3.9% (pooled analysis from ACTION Study Group, Prof. G. Montalescot at Pitié-Salpêtrière Hospital).

About the APPOSITION IV Study
APPOSITION IV is a prospective, randomized, two-arm, multi-center study designed to compare the apposition of the STENTYS Sirolimus-eluting stent with Medtronic Resolute® in 150 patients suffering from ST-elevation Myocardial Infarction. Patients will be followed up at either 4 or 9 months (double randomization). The powered primary endpoint is strut apposition at 9 months under OCT. The secondary endpoints are strut apposition at 4 months under OCT, and strut coverage at 4 and 9 months. The first results are expected to be announced in H2 2013.

About the APPOSITION V
Study APPOSITION V is a prospective, multi-center, randomized, two-arm clinical trial to evaluate the safety and effectiveness of the STENTYS Self-Apposing® stent in the treatment of de novo stenotic lesions in coronary arteries in 880 patients undergoing revascularization due to ST-elevation myocardial infarction (STEMI) as compared to the Multi-Link stent (Abbott Vascular, Inc.). The trial’s primary endpoint is target vessel failure (TVF), which is defined as a composite of cardiac death, target vessel recurrent myocardial infarction or clinically driven target vessel revascularization (TVR) at 12 months post-procedure. The powered secondary endpoint is acute stent malapposition and will be assessed by intravascular ultrasound (IVUS) on the first 225 patients. All patients will undergo clinical follow up at 30 days, six months, nine months and 12 months, with an annual checkup through three years. Fifty sites are expected to participate in the U.S. and worldwide. Enrollment is expected to begin in H1 2013.

About STENTYS
STENTYS is developing and commercializing innovative solutions for the treatment of patients with acute myocardial infarction (AMI, or heart attack) and complex coronary artery disease. STENTYS’ Self-Apposing® stents are designed to adapt to vessels with ambiguous or fluctuating diameters, particularly in the post-infarction phase, in order to prevent the malapposition problems associated with conventional stents. In the APPOSITION III clinical trial, STENTYS stents demonstrated a very low one year mortality rate among 1,000 high-risk AMI patients when compared to recent studies with conventional stents. More information is available at www.stentys.com.
This press release contains forward looking statements about the Company’s business. Such forward looking statements are based on numerous assumptions regarding the Company’s present and future business strategies and the environment in which it will operate in the future which may not be accurate. Such forward-looking statements involve known and unknown risks which may cause the Company’s actual results, performance or achievements to differ materially from any future results, performance or achievements expressed or implied by such forward-looking statements. Such factors include, among others, risks associated with the development and commercialization of the Company’s products, market acceptance of the Company’s products, its ability to manage growth, the competitive environment in relation to its business area and markets, its ability to enforce and protect its patents and proprietary rights, uncertainties related to the U.S. FDA approval process, including with respect to a pre-market approval for the Company’s BMS, slower than expected rates of patient recruitment for clinical trials, the outcome of clinical trials, and other factors, including those described in the Section 4 “Risk Factors” of the Company’s 2011 Registration Document (document de référence) filed with the Autorité des marchés financiers in France on June 25, 2012 under number R.12-033 as such section may be updated from time to time.

STENTYS
Stanislas Piot, CFO
Tel.: +33 (0)1 44 53 99 42
stan.p@stentys.com
STENTYS is listed on Comp. C of the NYSE Euronext Paris
ISIN: FR0010949404 – Ticker: STNT
Europe: NewCap.
Dusan Oresansky / Pierre Laurent
Tel.: +33 (0)1 44 71 94 93
stentys@newcap.fr
US: MacDougall Biomedical Communications
Charles Liles, Tel.: 781 235 3060
Christine Labaree, Tel.: 650 339 7533
stentys@macbiocom.com

16/04/2013

April 16, 2013

Auris Medical, a company dedicated to the development of novel therapeutics for the treatment of inner ear disorders, announced today the completion of a CHF 47.1 million1 Series C financing. Two leading venture capital firms, Sofinnova Ventures (Menlo Park, CA USA) and Sofinnova Partners (Paris, France), participated in the financing. The funding will enable Auris Medical to advance its two clinical projects, AM-101 for the treatment of acute tinnitus and AM-111 for the treatment of acute inner ear hearing loss, through Phase III studies and ultimately to market launch. In connection with the fund raising, Jim Healy, MD, PhD, General Partner at Sofinnova Ventures, and Antoine Papiernik, MBA, Managing Partner at Sofinnova Partners, joined Auris Medical’s Board of Directors.

« The Series C financing represents an important milestone on our way to bring safe and effective therapies to the many patients suffering world-wide from tinnitus or hearing loss for whom today no proven drug-based treatment options exist », said Thomas Meyer, Auris Medical’s founder and Managing Director. « Having established proof of concept in Phase IIb studies, we are now ready to move forward with our clinical devel-opment plans. Thanks to this latest financing round our leadership position in the emerging market for inner ear therapeutics will be further strengthened. »

« We are impressed with the significant clinical progress that Auris Medical has made towards developing first-in-class therapeutics for two inner ear disorders, » commented Jim Healy. « We are pleased to bring our expertise and network to back Auris Medical’s team and help them build a successful and global business. » Antoine Papiernik stated: « We are thrilled to support Auris Medical’s development at this important time in its life. The company has developed a unique set of compounds that could ultimately address an important unmet medical need. »

About Auris Medical
Auris Medical is a Swiss biotechnology company developing specific pharmaceutical compounds for the prevention or treatment of inner ear disorders, an area of great unmet medical need. The Company is cur-rently focusing on the development of treatments for acute inner ear tinnitus (AM-101) and for acute inner ear hearing loss (AM-111) by way of intratympanic injection with biocompatible gel formulations. AM-101 contains a small molecule NMDA receptor antagonist. In a Phase IIb clinical trial the treatment showed a statistically significant reduction in tinnitus loudness and several other outcomes in patients suffering from acute tinnitus with established cochlear origin. AM-111 contains a cell-permeable peptide that selectively blocks JNK signalling involved in apoptosis and inflammation. A recent Phase IIb clinical trial demonstrated a statistically significant improvement in the hearing and speech discrimination of patients with severe to profound hearing loss. In addition, Auris Medical is pursuing some early-stage research and development projects.
1 About USD 50.4 mn / EUR 38.6 mn at current exchange rates

About Sofinnova Ventures
Sofinnova Ventures has over 40 years of experience building healthcare companies into market leaders. With USD 1.4 bn in committed capital, the firm applies capital and expertise to take companies from incep-tion to exit. Sofinnova closed its life science-focused USD 440 mn fund, SVP VIII, in late 2011. The firm’s investment team of MDs and PhDs has significant scientific, operational and strategic experience, and spe-cializes in financing later stage clinical products and growth companies. Our team partners with entrepre-neurs to address patients’ unmet medical needs. Sofinnova Ventures has offices in Menlo Park and La Jolla, California.
For more information, please visit www.sofinnova.com.

About Sofinnova Partners
Sofinnova Partners is an independent venture capital firm based in Paris, France. For 40 years, the firm has backed nearly 500 companies at different stages of their development – pure creations, spin-offs, as well as turnaround situations – and worked alongside Europe’s key entrepreneurs in the Life Sciences industry. With EUR 1.3 bn of funds under management, Sofinnova Partners has created market leaders with its experi-enced team and hands-on approach in building portfolio companies through to exit.
For more information, please visit sofinnova.social-unit.fr.

Contact for Auris Medical
Thomas Meyer, +41 61 201 13 50, tm@aurismedical.com
Contact for Sofinnova Ventures
Jennifer James, +1 650 681 8429, jennifer@sofinnova.com
Contact for Sofinnova Partners
Anne Rein, +33 6 03 35 92 05, anne.rein@strategiesimage.fr

16/04/2013

Basée à Bâle (Suisse), Auris Medical développe des traitements innovants contre les dysfonctionnements de l’oreille interne. L’investissement va permettre de financer le développement clinique de Phase III et la mise sur le marché de ses deux produits phares : AM-101, un traitement contre les acouphènes et AM-111, un traitement contre la perte d’audition de l’oreille interne.
Antoine Papiernik, Partner Associé chez Sofinnova Partners, déclare : “ Nous sommes ravis de soutenir un entrepreneur aussi talentueux que Thomas Meyer. Nous avons suivi Auris Medical depuis ses débuts en 2003, et alors que l’entreprise entame une phase décisive de son développement, Sofinnova Partners est heureux de pouvoir y contribuer en apportant son expertise et son réseau. Les dysfonctionnements de l’oreille interne sont en augmentation constante dans le monde, alors qu’aucun traitement innovant n’aie vu le jour depuis longtemps. Auris Medical est l’un des acteurs les plus avancés au monde dans ce domaine, avec des produits qui pourrait véritablement répondre à ces besoins médicaux importants».

11/04/2013

Paris, le 12 avril 2013. Sofinnova Partners, société de capital-risque basée à Paris, annonce le succès de l’introduction en bourse d’Omthera Pharmaceuticals sur le NASDAQ Global Market de New York. Sofinnova Partners accompagne la société spécialisée dans le traitement des maladies cardiovasculaires depuis sa création en 2008. Seul investisseur du tour A, Sofinnova Partners demeurait le premier actionnaire au moment de l’introduction en bourse qui a permis de lever 64 M$ (48,8 M€).
Basée à Princeton (New Jersey, Etats Unis), Omthera Pharmaceuticals est spécialisée dans le traitement de la dislipidémie, à l’origine de nombreuses maladies cardiovasculaires. Cette levée de fonds va permettre à la société d’accélérer le développement et la commercialisation aux Etats Unis de son produit phare Epanova.
Graziano Seghezzi, Associé chez Sofinnova Partners, et membre du Conseil d’administration d’Omthera Pharmaceuticals, déclare : « Je connais le talent de Jerry Wisler, co-fondateur d’Omthera Pharmaceuticals, pour l’avoir accompagné lors de ses précédentes aventures entrepreneuriales, et suis ravi d’avoir contribué à la création d’Omthera Pharmaceuticals ainsi qu’à cette nouvelle étape du développement de la société. Omthera Pharmaceuticals illustre parfaitement notre stratégie qui consiste à accompagner le plus loin possible les entrepreneurs visionnaires qui développent des technologies de rupture sur des marchés porteurs ».
L’’introduction en bourse a porté sur 8 millions de titres dont le prix a été fixé à 8$. La cotation sur le NASDAQ Global Market a démarrée le 11 avril 2013 sous le symbole « OMTH ». Se référer au communiqué de la société (en PJ) pour de amples informations sur l’opération.
A propos de Sofinnova Partners
Sofinnova Partners est une société de capital-risque indépendante basée à Paris. Depuis 40 ans, la société a financé près de 500 sociétés – start-up, spin-off et opérations de retournement. Elle a accompagné les plus grands entrepreneurs européens dans le domaine des sciences de la vie. Avec 1,3 milliard d’euros sous gestion, l’équipe de Sofinnova Partners, reconnue pour sa capacité à aider et à soutenir les entreprises de son portefeuille de la création à la sortie, a permis l’émergence de leaders sur leurs marchés.

Contact presse pour Sofinnova Partners
Anne Rein
STRATEGIES & IMAGE
Tel: +33 6 03 35 92 05
anne.rein@strategiesimage.com