German Biotech gets Seed Funding to Repurpose Cancer Drugs for the Flu By Clara Rodríguez Fernández 2 minutesmins February 8, 2017 -Updated: onJune 22, 2022 2 minutesmins Share WhatsApp Twitter Linkedin Email Newsletter Signup - Under Article / In Page"*" indicates required fieldsCompanyThis field is for validation purposes and should be left unchanged.Subscribe to our newsletter to get the latest biotech news!By clicking this I agree to receive Labiotech's newsletter and understand that my personal data will be processed according to the Privacy Policy.*Company name*Job title*Business email* Atriva Therapeutics has received seed funding to advance the development of a better therapy for influenza in patients at high risk.Atriva Therapeutics was founded in Tübingen, Germany in 2015 with a quite particular aim: repurposing cancer drugs to treat influenza. Two private investors, the Dutch Stichting Participatie Atriva and the German High-Tech Gründerfonds (HTGF) have contributed with an undisclosed amount of seed funding that will help the young biotech push its first drug candidate to the clinic.Atriva’s lead candidate, ATR-002, is expected to enter clinical trials in 2018. The drug is intended for treating influenza in high-risk patients with severe respiratory complications due to bacterial co-infections. These cases exceed 12 million annually and there’s no therapy available for them. Current medications, neuraminidase inhibitors, are not approved in this patient group because of lack of efficacy. The German biotech wants to change this situation by repurposing oncology drugs that are already approved or in advanced clinical development for the treatment of influenza. The compounds in question are MEK inhibitors, which target intracellular signaling factors essential for viral replication.Influenza virusCompared to existing influenza drugs such as Tamiflu (oseltamivir), MEK inhibitors have a larger therapeutic time, no risk of inducing resistance and can suppress dangerous bacterial co-infections of the lungs. In addition, available safety and tolerability data from previous trials can shorten the development time.Atriva Therapeutics estimates that the accessible global market potential of its MEK inhibitors could exceed €2.8Bn in 2020. And that’s without counting stock-piling of influenza therapeutics for the prevention of pandemics.With clear advantages over existing drugs, the company could make a big entrance in the market. However, it will have to watch out for indirect competitors, such as Humabs‘ antibody against influenza A or Sanofi‘s universal flu vaccine.Images from Irina Bg /Shutterstock, Atriva Therapeutics Advancements in antimalarial drug discovery and development This webinar explores how recent innovations are transforming antimalarial drug discovery and development. Discover how advanced screening techniques, novel compound development, and data-driven decision-making empower researchers to accelerate candidate selection, overcome parasite resistance, and enhance therapeutic efficacy across the R&D pipeline. Watch now on-demand Explore other topics: GermanyInfectious disease ADVERTISEMENT