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Facio raises €8M in equity financing

Facio Therapies announced today that it had successfully completed an equity financing round with proceeds of €8M (approximately A$12.5M; C$12M; US$9M). FSHD Spain and 30 other members of the FSHD community newly invested alongside existing investors, including Facio’s drug discovery partner, Evotec. Facio will use these funds to expand its recently announced in vivoproof of principle and to advance selected lead candidates towards clinical studies.

The key event in FSHD is the undue production of the DUX4 protein in skeletal muscle. DUX4 sets in motion a cascade of biochemical events that eventually result in the devastating effects of FSHD. In people without FSHD, the production of DUX4 in skeletal muscle is repressed by regulatory mechanisms. Facio’s single goal is to develop therapies that restore this repression as much as possible. Facio is the only one in the FSHD field with a fully automated, high-throughput screening platform based on quantifying the DUX4 protein in unadulterated (“primary”) FSHD-affected muscle cells. Recently, Facio delivered the first-ever proof of principle in FSHD using one of its lead candidates in a unique FSHD-relevant animal model (“in vivo”).

Three FSHD-affected families founded Facio in September 2014. Since then, Facio has raised over €16M in equity. About 77% of that amount has been invested by members of the FSHD community. Facio’s investor base now spans 14 countries around the world. FSHD Spain became the fifth FSHD foundation to invest in Facio, joining Amis FSH(France), FSHD Canada, FSHD Global Research (Australia), and the FSHD Stichting (Netherlands).

“The success of this financing round is not only that we reached our goal of raising €8 million,” said Facio’s Chairman, Kees van der Graaf. “The success is just as well that Facio’s message resonates with an ever-growing number of FSHD-affected families across the globe. We, people living with FSHD, don’t have to wait and hope for a breakthrough to happen. We’re breaking through to therapy ourselves. That is Facio’s message.”

Source: Facio

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HollandBIO Kijk- en Leestip: het verhaal van Keytruda

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Voor HollandBIO kan een dag bijna niet beter beginnen: het FD openslaan en lezen ‘hoe een Nederlands middel tegen kanker de wereld verovert’. Een prachtige reconstructie van Thieu Vaessen over de Nederlandse roots van Keytruda, of Pembrolizumab, een innovatief medicijn tegen kanker dat soms spectaculaire resultaten laat zien. En als je dan na een lange werkdag thuiskomt en Aduro Biotech’s Hans van Eenennaam samen met een dankzij ‘Pembro’ weer gezonde patiënt ziet schitteren in De Wereld Draait Door, kan de dag echt niet meer stuk. Koplopers uit de Nederlandse biotech volop in de schijnwerpers, zo zien we het graag! Lees terug, kijk terug, en wees trots op onze prachtige sector.

 

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ttopstart joins PNO Group

ttopstart and PNO will join forces in their ambition to become Europe’s leading consultancy in strategy and funding services in life sciences and health. Together, ttopstart-PNO will now have 50 life sciences professionals located in 6 European countries.

ttopstart was founded in 2009 as a university spin-off from the VU University in Amsterdam. Since then, the company has rapidly grown into one of the leading consultancy companies in the field of life sciences and health. The collaboration with PNO Group is the next step to accelerate further growth of the company.

Read more

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Cargill and Royal DSM to establish joint venture Avansya: to bring zero-calorie, cost-effective sweeteners to market faster

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Avansya venture to help food and beverage producers deliver the products and brands consumers love, with significantly reduced calories

As food and beverage producers look to significantly reduce calories in their offerings to consumers, they are in need of non-artificial, zero-calorie, great-tasting sweetener options. Today,Cargill and Royal DSM, a global science-based company in Nutrition, Health and Sustainable Living, announced a new joint venture, Avansya, to rise to this challenge. Together, the companies will produce highly sought-after, sweet-tasting molecules, such as steviol glycosides Reb M and Reb D through fermentation, giving food and beverage manufacturers an even more scalable, sustainable and low cost-in-use solution than if these same molecules were extracted from the stevia leaf.

The new venture will combine both companies’ technologies for producing steviol glycoside products made through fermentation and will market its products under one brand name, EverSweet™.

The joint venture will be a 50-50 partnership between the two companies. The establishment of the joint venture is subject to regulatory approvals and other customary closing conditions but expected to be finalized in the first calendar quarter of 2019.

The partnership leverages the two companies’ highly complementary strengths for bringing to market fermentation-derived Reb M and Reb D steviol glycosides:

  • DSM brings its leading biotechnology know-how, providing R&D expertise, including strain development and fermentation process development capabilities, as well as customer relationships in specific market segments;
  • Cargill brings its unrivalled application expertise and global commercial footprint in the sweetener market, as well as large-scale fermentation capacity with access to co-located, raw material suppliers at its Blair, Nebraska (USA) site.

The joint venture will make use of a new fermentation facility being built at the site in Blair, which is expected to be completed and operating in summer 2019.

“We are delighted to announce this game-changing joint venture with Cargill,” said DSM Food Specialties President, Patrick Niels. “One of the most significant transformations in global food & beverage markets is the drive to reduce sugar in people’s diets. This partnership will allow us to bring sustainably produced sugar-reduction solutions based on steviol glycosides to market faster and more effectively at a scale to deliver global impact. Both DSM and Cargill are purpose-led companies. We want to positively impact our societies, enable our customers’ brands and businesses to be successful in their markets, and in doing so support our own further growth.”

“The demand for sugar-reduction solutions is urgent, global, and growing fast,” said Cargill Vice President Food Segment North America, Chris Simons. “While consumers are searching out foods and beverages that help meet their dietary needs or goals, whether for a diabetic diet or simply reducing calories and sugar intake, brand-owners know that great taste can’t be compromised. By partnering with DSM, we can further advance a commercialized Reb M & Reb D product line that offers what consumers desire.”

Source: DSM

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LSP raises record €750M in 10 months for life sciences innovations

LSP, the specialist life sciences and health care investment group, has raised more than €750 million for three different funds over the past ten months to invest in innovative drug development and medical technology companies across Europe. This result constitutes a record fundraise in European life sciences, consolidating LSP’s leading position.
2018 has been a landmark year for fundraising in the European life sciences industry. Over €3 billion has been raised to date, with institutions being drawn to the non-cyclical nature of the strategy, recognising the enormous potential of the life sciences industry in Europe and increasingly focusing on the social impact of their investments.
LSP has developed over 120 companies since its inception in 1998, of which many have brought innovative drugs or medical technologies to the patient community. The firm has assets under management of over €2 billion in nine funds and has offices in Amsterdam, Munich and Boston.
“We have been delighted by the support we have received from both new and existing investors,” said Dr René Kuijten, managing partner of LSP. “I believe that our fundraising success is based on a number of factors: the increased efficiency and maturity of the European VC ecosystem; a shift in big pharma and medtech from an internal R&D to an acquisition-based model; and the performance of our funds”.
The European biotech and medical technology market has matured significantly over the last decade, becoming increasingly efficient at commercialising scientific innovation. The number of repeat entrepreneurs is a testament to this, with about one third of LSP’s new investments coming from entrepreneurs with whom the firm has had previous successes.
In its home markets of the Benelux and German speaking regions of Europe, LSP has played a key role in harnessing support for life science ventures. Earlier this year, LSP’s Rudy Dekeyser and René Kuijten catalysed the foundation of the Oncode Institute in the Netherlands, which brings together 600 of the best oncology researchers in one single institute. Supported by the Dutch government, Dutch Cancer Society and nine Dutch research institutes, Oncode helps commercialise breakthrough discoveries and get them to patients faster.
Big pharma companies have shifted their business model, no longer relying solely on internal R&D to develop new products but rather acquiring VC backed start-ups and listed small-cap companies at a later stage. Today, at least two-thirds of new drugs coming on to market originate from universities and life sciences start-ups. LSP portfolio companies currently have over 100 products in patient trials, a pipeline larger than many of the leading pharma groups like Pfizer, Sanofi, GSK and Novartis.
LSP analyses more than 1,000 investment opportunities per year and thus can be very selective.  The firm has built a stable team that has been together for an average of 15 years. LSP’s collegiate approach is designed to allow for growing companies and delivering new drugs and technologies to patients whilst generating superior returns for investors. Recent successes include argenx (auto-immune diseases; current value $3.5 billion); Neuravi (minimal invasive stroke treatment, successfully sold to J&J); and Amarin (cardiovascular disease; current value over $7 billion). In total, over the past five years alone, LSP has sold 23 companies.
Existing and new investors in LSP’s strategies include blue-chip insurance companies, pension funds, government funds, asset managers, family offices and, in particular, big pharma.  For example, LSP 6 has been selected by Bristol-Myers Squibb to be its venture group of choice in Europe, following similar LSP relationships with GSK and Pfizer. Working closely with a pharma company provides LSP with deep insight into pharma’s thinking, enhancing its understanding of which companies are most likely to be attractive M&A targets.
Source: LSPVC
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Catalyze wins FD Gazellen award

Earlier this year Catalyze opened new offices in Denmark and Switzerland, becoming a truly international company with its headquarter in Amsterdam. Now, Catalyze receives a FD Gazellen award, meaning that it is one of the fastest growing companies in the Netherlands.

“We are very proud to receive this award. It is a great acknowledgement for our journey so far and all of our employees working hard every day to realize our dream. At the same time, we have high ambitions for the future and this is still just the beginning.” – Theodoor Rutgers, founder and director.

Catalyze is the market leader in raising non-dilutive funding for companies and researchers active in the Life Sciences sector, having raised more than €500 million since their foundation in 2014. The company grew more than 20% each year for the past 3 years (an impressive feat considering its sector), comprising now 65 employees at 5 locations.

“We are not only specialized in funding, but we also deliver a broader range of strategic consulting services to support our clients. Both our service offering and client portfolio continue to expand. No matter how you identify Catalyze: we are unique and distinctive.” – Commercial Director Quirein te Roller speaking about Catalyze, internationally active in more than 30 countries.

The ambitious and innovative consultancy company is an absolute specialist in obtaining funding and has a broad experience with a variety of subsidies, government guaranteed loans and tax incentive schemes like Eurostars, Horizon2020, ERC and NIH.

Source: Catalyze

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Vlaanderen en Nederland bundelen krachten op het gebied van Personalised Medicine

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Tijdens de Vlaams-Nederlandse politieke topontmoeting op 5 november in Middelburg is een Memorandum of Understanding (MoU) ondertekend door staatssecretaris Mona Keijzer van het ministerie van Economische Zaken en Klimaat (EZK) en Secretaris-generaal Johan Hanssens namens Minister Muyters van het Vlaamse departement van Economie, Wetenschap en Innovatie (EWI) op het gebied van Personalised Medicine. Hiermee wordt samenwerking tussen de Lage Landen op dit thema versterkt voor de komende vijf jaar.

 

Vlaanderen en Nederland werken al twee jaar succesvol samen aan   regeneratieve geneeskunde, middels een publiek-private samenwerking genaamd Regenerative Medicine Crossing Borders (RegMed XB). Een uitbreiding van de samenwerking tussen de Lage Landen op een breed scala van onderwerpen binnen personalised medicine lijkt dan ook een mooie vervolgstap. De ondertekening van het MoU op 5 november heeft als doel om de komende vijf jaar intensief samen te werken aan missiegedreven onderzoek en ontwikkeling, innovatie en ondernemerschap op het gebied van de  personalised medicine. Met de MoU beogen Vlaanderen en Nederland de krachten van zowel private als publieke partijen over de landsgrenzen te bundelen.

 

De ondertekening van het MoU vond plaats in het bijzijn van minister-president Rutte en zijn Vlaamse ambtsgenoot Bourgeois en wordt in het voorjaar van 2019 opgevolgd door een gedetailleerde onderzoeksagenda. Deze agenda betreft in ieder geval  het bestaande subthema regeneratieve geneeskunde, maar ook de additionele subthema’s: cell-based technologies; preventie en leefstijlgeneeskunde; personal data infrastructuur en management. Hiermee vormen Vlaanderen en Nederland een gezamenlijke agenda waarin de ambities staan voor baanbrekende technologieën als Organ-on-a-Chip en data FAIR principes. Door het bundelen van krachten over de grens worden  nieuwe combinaties van expertises en technologieën samengebracht, die vervolg opgeschaald kunnen worden en beschikbaar komen voor grote groepen patiënten.

 

De Topsector Life Sciences & Health (Health~Holland) werkt komende maanden aan het programma en de onderzoeksagenda samen met het ministerie van EZK, het departement EWI en betrokken stakeholders.

 

Bron: Health-Holland

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Website PharmInvestHolland gelanceerd

Hoe verzilveren we de kansen voor de Nederlandse biofarmaceutische sector? De recent gelanceerde website van PharmInvestHolland laat zien hoe de sector werkt aan het verder versterken en voor het voetlicht brengen van het aantrekkelijke R&D-klimaat voor biofarmaceutische bedrijven in Nederland. Dit leidt niet alleen tot meer onderzoek en ontwikkeling, maar draagt ook bij aan meer banen, meer innovatie in de gezondheidszorg en een grotere bijdrage van de sector aan de Nederlandse economie.

PharmInvestHolland is een samenwerkingsverband dat in 2017 is opgericht onder de vlag van de Topsector Life Sciences & Health, Health~Holland. De brede vertegenwoordiging van partners uit de geneesmiddelensector werkt gezamenlijk aan de verwezenlijking van de ambitie dat Nederland de biofarmaceutische hotspot van Europa wordt. Zo is recent een bidbook uitgebracht met daarin de Nederlandse propositie als meest aantrekkelijke vestigingslocatie in Europa voor biofarmaceutische bedrijven.

Partners PharmInvestHolland
De samenwerkende partijen binnen PharmInvestHolland zijn AmCham, Health~Holland, HollandBIO, Lygature, het ministerie van Economische Zaken en Klimaat, de Netherlands Foreign Investment Agency, de Vereniging Innovatieve Geneesmiddelen en VNO-NCW.

Voor de website, klik hier.

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Price Controls Would Harm Drug Discovery and Innovation, New Report Shows

As the Trump administration considers policy price controls on drugs, a new report released today by the Information Technology and Innovation Foundation (ITIF), the world’s top-ranked science and technology policy think tank, highlights how price controls would have a negative effect on drug development by reducing biopharmaceutical industry investment in research, thereby slowing the pace of drug discovery. Further, price controls would damage the overall life-sciences innovation ecosystem by reducing knowledge sharing between firms.

“Biomedical innovation is critical to addressing the country’s health challenges, but developing a new drug costs between $1.5 to $2.6 billion,” said ITIF President Rob Atkinson, author of the report. “Price controls and other steps to limit prices, such as weaker intellectual property protections, would lead to less R&D and would limit overall knowledge generation and sharing critical to new drug discovery.”

The report shows that biopharmaceutical firms contribute to the overall drug innovation ecosystem because the research and development (R&D) they fund spills over both to other firms and to the public domain, helping to spur more life-sciences innovation. The report also highlights how biopharmaceutical firms contribute to knowledge sharing through providing over $2.5 billion annually for university research in all fifty states, contributing to open science through over 12,500 publications in science journals in 2017, and participating in other activities such as open consortia designed to develop and disseminate discoveries.

“Price controls will slow the pace of drug innovation, and future generations will pay the price,” Atkinson said. “Without the knowledge generation that R&D stimulates, the next generation of Americans will be left with drugs that will be less effective than they could have been.”

Read the report here.

Source: ITIF

The Information Technology and Innovation Foundation (ITIF) is an independent, nonpartisan research and educational institute focusing on the intersection of technological innovation and public policy. Recognized as the world’s leading science and technology think tank, ITIF’s mission is to formulate and promote policy solutions that accelerate innovation and boost productivity to spur growth, opportunity, and progress.

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IV-WALK WINT VINTURA IMPACT IN HEALTHCARE AWARD 2018

Tijdens het Impact in Healthcare event streden afgelopen donderdag drie initiatieven om de Vintura Impact in Healthcare award. Het publiek en de vakjury kozen na drie gepassioneerde pitches de IV-Walk als winnaar. De andere twee genomineerden waren eNose en NightWatch.

 

IV-Walk: prijs helpt mij met het zetten van de volgende stap

IV-Walk is een draagbaar infuus waarmee de patiënt zich makkelijk kan bewegen en wat de mobiliteit en het herstel bevordert. Designer Alissa Rees ontwikkelde IV-Walk gebaseerd op haar eigen ervaringen. Ze had zelf ondervonden hoe beperkend een infuuspaal kan zijn als je deze wekenlang 24 uur per dag bij je moet hebben. Alissa Rees: “Met IV-Walk kun je makkelijk even naar buiten of van de afdeling af en blijf je niet snel hangen achter een deurklink”. Rees zou graag een team van specialisten willen betrekken bij de doorontwikkeling van IV-Walk. “Met deze prijs wil ik graag een volgende stap zetten: van goed idee naar de markt. Daarnaast zou ik de prijs graag willen gebruiken voor de ontwikkeling van een kinderversie.”

 

Vakjury over IV-Walk

De vakjury bestond uit Margriet Schneider (UMC Utrecht), Michele Manto (Galapagos), Daan Rooijmans (CZ Zorgverzekeringen), Hans Bart (Nierpatiënten Vereniging Nederland) en Bas Amesz (Vintura). Samen met het publiek kozen ze IV-Walk als winnaar. Bas Amesz, partner Vintura, licht toe: “Juist omdat dit product, een prachtig ontworpen draagbaar infuus, zo vanzelfsprekend is, heeft het een enorme levensvatbaarheid. Je voelt ook aan alles dat Alissa IV-Walk met passie heeft ontwikkeld. Zij staat volledig voor haar eigen idee“. IV-Walk ontvangt met deze award een prijs van €10.000 en 5 Vintura consultancydagen. Bas Amesz: “Juist een start-up als deze kan de prijs goed gebruiken om de volgende stap te nemen. Wij zijn blij dat we haar als Vintura hierbij kunnen helpen.“

 

Waardevolle feedback

Alle drie de genomineerden (naast IV-Walk waren dat eNose en NightWatch) kregen waardevolle feedback tijdens interactieve sessies met de aanwezigen, ca. 80 bestuurders en senior managers van ziekenhuizen en andere zorginstellingen, zorgverzekeraars, life sciences en patiëntorganisaties.

Met het organiseren van dit event wil Vintura de verschillende stakeholders dichter bij elkaar brengen en een boost geven aan jonge, baanbrekende initiatieven die grote impact voor de patiënt (kunnen) hebben. Zo wil Vintura een bijdrage leveren aan het realiseren van betere zorg die beschikbaar én betaalbaar is voor alle patiënten.

 

Bijna 20 inzendingen

In totaal waren er dit jaar bijna 20 inzendingen voor de Impact in Healthcare award. De jury was zeer verheugd over de hoge kwaliteit van de inzendingen en heeft getoetst in hoeverre de initiatieven voldeden aan de opgestelde criteria rondom ‘innovativiteit, ‘impact’, ‘schaalbaarheid’ en ‘samenwerking’.

© 2018 foto: Juliette Moulen Photography