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Drug development booms in Medicon Valley
When it comes to developing new medicines, the Öresund region is one of the top performers in the EU. Companies working on commission for pharmaceutical companies are highlighted as a success factor. “Everyone has heard of Novo Nordisk, but these companies are unknown to people outside the industry despite being the golden vein of the life science sector,” says Anette Steenberg, CEO of the cluster organisation MVA.
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Stark pipeline i Medicon Valley – servicebolagen lyfts fram
Öresundsregionen har en av toppositionerna i EU vad gäller utveckling av nya läkemedel. Företag som arbetar på uppdrag av läkemedelsbolag lyfts fram som en framgångsfaktor. ”Alla känner till Novo Nordisk, men de här företagen har ingen utanför branschen hört talas om trots att de är life science-sektorns gyllene ven”, säger Anette Steenberg, vd för klusterorganisationen MVA.
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Ansökan klar för enklare doseringsform av lecanemab
En ansökan om marknadsgodkännande i USA har nu slutförts för det svenskutvecklade Alzheimerläkemedlet lecanemab som veckovis subkutan underhållsbehandling.
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New large lab building in Lund inaugurated – here are the companies moving in
Medicon Village has received a new laboratory building. On Friday last week the building was inaugurated with a ribbon-cutting ceremony by Minister for Employment and Integration Mats Persson (L) and construction contractor Mats Paulsson.
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An increasing number of people are falling ill with TBE – “Much more research is needed”
Tick-borne meningitis, or TBE, is an increasingly common disease in Sweden. Currently, there is a vaccine against the disease but no drugs. Researcher Anna Överby Wernstedt is studying the processes that occur in the brain during a TBE infection and hopes to contribute to developing a treatment.
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Hon ska leda affärsutvecklingen på Diamyd i Umeå
Diamyd Medical, som utvecklar läkemedel mot typ 1-diabetes, har anställt Sofia Mayans som affärsutvecklingschef vid företagets produktionsanläggning i Umeå.
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Leo Pharmas nyförvärv floppade i studie
Danska Leo Pharmas läkemedelskandidat mot hudsjukdomen kongenial iktyos har misslyckats i en fas III-studie.
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Nytt steg närmare marknaden för Sobis giktläkemedel
Läkemedelsutvecklaren Sobi har inlett en stegvis ansökan om marknadsgodkännande i USA för bolagets nya giktläkemedel Sel-212.
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Sofia Wallström is Lif's new CEO
Sofia Wallström has been appointed as the new CEO of the industry organization Lif, the trade association for the research-based pharmaceutical industry in Sweden.
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Innovative start-up helps doctors, scientists and industry balance coagulation risks
For many doctors caring for seriously ill patients, for example, in stroke units and cancer wards, maintaining the life-saving balance between bleeding and thrombosis is an ongoing challenge. In the late 1980s, scientists at Maastricht University in the Netherlands developed an innovative method, the thrombin generation assay (TGA), which provides a complete overview of a physiological process crucial for maintaining normal haemostasis.
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Ny doseringsform öppnar för enklare behandling med lecanemab
En ansökan om marknadsgodkännande i USA har påbörjats för det svenskutvecklade Alzheimerläkemedlet lecanemab i subkutan form.
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Carl Borrebaeck – professor and serial entrepreneur with a taste for speed
Award-winning cancer researcher, the founder of many listed companies, and constantly in the academic and commercial spotlight for decades. However, Carl Borrebaeck, Professor of Immunotechnology at Lund, is not yet satisfied. “We have a new, potentially super exciting project in the pipeline,” he says.
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Recipharm divests five Swedish plants
Swedish contract manufacturer Recipharm is selling its facilities in Solna, Strängnäs, Höganäs, Karlskoga and Uppsala OTC Development to US private equity company Blue Wolf Capital Partners.
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“Don’t postpone the transition to IVDR”
Operators who have not yet started to adapt to the requirements of the new EU IVDR regulation are running out of excuses. This is the opinion of Helena Dzojic, Head of Unit at the Swedish Medical Products Agency, who continues to persistently spread her message: don’t postpone the transition.
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To build trust, one must be able to say “I don’t know” – whether human or AI
Will AI strengthen or break down trust? It depends on whether we can understand and accept its limitations, and our own, writes Sarah Lidé in a column.
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Minskade dödlighet med 27 procent i studie – cancervaccin godkänns som särläkemedel
Det nya cancervaccinet från Ultimovacs får nu status som särläkemedel i EU. "Ett viktigt steg", enligt vd:n.
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Diamyd får snabbspår i USA – ”Oerhört glada”
Svenska Diamyd Medical har beviljats ”Fast Track Designation” – ett snabbspår – av amerikanska FDA för sin immunoterapi under utveckling för patienter med typ 1-diabetes.
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The Swedish Research Council gets go-ahead for more long-term funding
Following a government decision, the Swedish Research Council will soon be able to approve ten-year grant periods for funding research infrastructure, which may affect the giant Max IV project, among others.
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Rising interest in CRISPR treatments
Treatments using CRISPR technology are emerging as one of the hottest medical trends in the United States – and the FDA is doing its best to promote the development.
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Stark uppgång för Crispr-behandlingar
Behandlingar som använder gensaxen Crispr växer fram som en av de hetaste medicinska trenderna i USA – och läkemedelsmyndigheten FDA gör sitt bästa för att stödja den utvecklingen.
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Anna Törner: “My quantified life”
“The expression ‘you can’t see the forest for the trees’ feels newly relevant in the context of wearables. One can easily get caught up in the idea that the more we measure, the more we know,” Anna Törner writes in a column.
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Cancervaccin får snabbspår i USA
Norska Ultimovacs har beviljats ett så kallat Fast Track Designation från den amerikanska läkemedelsmyndigheten, FDA, för sitt cancervaccin UV1.
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Failed to read the fine print – lost his life’s work
A celebrated CEO and co-founder of a pioneering lab company one moment – the next, fired, kicked out and written out of the company’s history. This is the story of a Swedish entrepreneur who was going to raise US venture capital to strengthen his company but lost his life’s work instead.
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Guard Therapeutics: ”Mötet med FDA är en tydlig validering av våra kliniska fas II-data”
Det svenska bioteknikföretaget Guard Therapeutics meddelar att de fått positiv återkoppling från den amerikanska läkemedelsmyndigheten, FDA, efter ett möte gällande deras läkemedelskandidat RMC-035.
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