AstraZeneca's MedImmune will collaborate with Johns Hopkins University in both biologics and small-molecule projects.
MedImmune, AstraZeneca’s global biologics research and development arm, and The Johns Hopkins University entered into a five-year, $6.5 million research collaboration, according to a joint press release. The joint research projects will focus on MedImmune’s therapeutic areas of interest, including cardiovascular and metabolic disease; oncology; respiratory, inflammation, and autoimmunity; infectious disease; and neuroscience. This new collaboration model extends to both MedImmune’s biologics and AstraZeneca’s small molecule portfolios.
In oncology, research will explore the role of immune system cells in tumor growth and harness findings to identify new cancer drug targets. In the areas of respiratory, inflammation, and autoimmunity, projects will research the damaging mechanisms underlying rheumatoid arthritis (RA) and validate potential therapeutic targets that may play key roles in the development or progression of RA. In infectious disease, projects will assess monoclonal antibody combinations to aid in clinical candidate selections to more effectively prevent recurrent infections in high-risk patients, such as those with diabetes. This collaboration builds on MedImmune’s ongoing work to prevent serious and costly drug-resistant infections. In antibody discovery and protein engineering, MedImmune will work with the university to find innovative ways to manufacture complex next generation biologic drugs.
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines
April 30th 2024In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
Drug Solutions Podcast: Gliding Through the Ins and Outs of the Pharma Supply Chain
November 14th 2023In this episode of the Drug Solutions podcast, Jill Murphy, former editor, speaks with Bourji Mourad, partnership director at ThermoSafe, about the supply chain in the pharmaceutical industry, specifically related to packaging, pharma air freight, and the pressure on suppliers with post-COVID-19 changes on delivery.
Understanding the Variability in Bioburden Test Results in Biomanufacturing
May 7th 2025This article explores the impact of test volume, microbial distribution, and dilution errors on bioburden testing variability. It presents statistical approaches to estimate percentage error and discusses strategies to optimize microbial enumeration techniques in biopharmaceutical quality control.
Trump Directs FDA, EPA to Reduce Regulatory Barriers to Domestic Pharma Manufacturing
May 7th 2025The White House is instructing FDA to increase fees for and inspections of foreign drug manufacturing plants and reduce the time required to approve such sites that will be newly constructed in the US.