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Thursday, April 6, 2023 | 11am ET / 8am PT In this webinar, we show how we used Nunchuck to make LNPs in small-volume screening runs and bulk formulations. The complete workflow will be illustrated, from the testing of flow rates in initial formulations to the final assessment of mRNA expression in multiple cell types, showing successful transfection of cells by the LNPs. Register now. 
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Today's Big NewsMar 30, 2023 |
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April 3 - 4, 2023 | San Diego, CA Be a part of a learning experience developed by our esteemed Advisory Board who are leaders in the life science communications space. Time is running out! Register Today  |
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| By Max Bayer Former Johnson & Johnson R&D chief Mathai Mammen has landed a new role, taking the reins as CEO of FogPharma. The well-financed biotech is aiming to launch its first asset into the clinic by the middle of the year. |
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By Nick Paul Taylor EIP Pharma has mapped out a financial freeway to the delivery of phase 2b on an ex-Vertex molecule. By merging with the floundering Diffusion Pharmaceuticals, the biotech is set to secure a Nasdaq listing and enough money to complete a clinical trial in dementia with Lewy bodies. |
By Gabrielle Masson Emerging biopharmas have gradually taken over the R&D pipeline, producing two-thirds of all new drugs in 2022, a finding one financial expert called "stunning." |
By Annalee Armstrong Gene editing has been limited to a few sites in the body because of restrictive delivery mechanisms. Scientists have now discovered a tiny needle that a bacteria uses to kill insect cells that could someday widen the world of gene editing therapeutics. |
By Nick Paul Taylor Confo Therapeutics’ business development team is on a roll. Weeks after licensing its lead candidate to Eli Lilly, the Belgian biotech has landed a 168 million euro deal with Daiichi Sankyo to discover small-molecule agonists of a central nervous system target. |
By Gabrielle Masson While clinical trial activity was strong in 2022 following a pandemic-induced dip, many trends resumed their pre-COVID trajectory—including plummeting diversity in clinical trials. |
By James Waldron Nanoscope has scored a phase 2 win for its gene therapy using light-sensitive molecules to treat retinal disease, keeping alive the hope of a first treatment to improve vision in these patients. |
By Max Bayer BriaCell is forming a new spinout company with the backend of its pipeline. The hope is that the assets can be better developed under a separate balance sheet. |
By Annalee Armstrong,Gabrielle Masson,Max Bayer We had hoped that our Layoff Tracker would stay retired for a while, but 2023 is starting to look a lot like our old friend 2022 when it comes to layoffs in biotech. |
By Conor Hale ICU Medical has placed itself in the running to serve as the new corporate home of Medtronic’s patient monitoring and hospital ventilator businesses, according to a report from Reuters. |
By Joseph Keenan Inato, a clinical trial company based in France, has hauled in $22 million in series A2 funding, which will be used for international growth, product innovation and to attract employees. |
By Kevin Dunleavy Based on 2021 spending data from the U.S. Centers for Medicare & Medicaid Services, Moody’s has identified drugs that appear destined to be subject to price negotiations in 2026. Bristol Myers Squibb and Pfizer’s Eliquis leads the pack, with drugs from AbbVie, Johnson & Johnson and Novo Nordisk also making appearances. |
By Robert King A new bipartisan Senate bill aims to crack down on Medicare Advantage up-coding that can drive up plan payments, hoping to settle a feud between CMS and health insurers. |
Fierce podcasts Don't miss an episode |
| This week on "The Top Line," we discuss Fierce Medtech’s annual Fierce 15 report and startups that made the cut. We also cover Illumina and Carl Icahn's proxy battle and more of this week's top headlines. |
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May 1 - 3, 2023 | Jersey City, NJ Connect with senior executives in Medical Affairs, MSL and IIT to share best practices. Register Today & save $200 from now until April 7th!
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Whitepaper Preparation of critical process liquids and buffer components shifts resources away from core activities and can be filled with inefficiencies and risks that can increase time and costs across your workflow. Learn about the framework to help reduce your total costs beyond capital and operational expenditures and set a solid foundation for successful scale-up of buffer preparation. Sponsored by: Thermo Scientific Production Chemicals and Services |
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Research Learn more on Catalent’s step-wise approach for the definition and execution of Process Characterization for the production of a monoclonal antibody for late phase process characterization and development. Sponsored by: Catalent |
Whitepaper Explore how clinical supply can be scaled up as decentralized programs progress, and how technological solutions can accelerate trial deployment. Sponsored by: Catalent Clinical Supply |
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Whitepaper For sponsors, cost is a key concern when it comes to managing the supply of their clinical trials. A financial project analyst (FPA) is a specialized expert who can help control clinical supply costs and keep the project within budget. Explore the critical role that a Financial Project Analyst plays in clinical trial supply and budget management. Sponsored by: Catalent |
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| May 1-3, 2023 | Jersey City, NJ |
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