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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 28, 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 Annalee Armstrong Novartis has hopped on Bicycle Therapeutics’ radio-conjugates ride with a $50 million upfront payment and a further $1.7 billion possible down the road. |
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By Nick Paul Taylor AbbVie has ditched its pact with CytomX Therapeutics. After seeing 83% of patients in the latest data cut develop anemia, the Big Pharma has dropped the cancer program for strategic portfolio reasons—and started negotiating to sell the lead antibody-drug conjugate back to CytomX. |
By Max Bayer Ferring Pharmaceuticals is closing up a U.S. research wing, laying off 89 employees as a result. The Ferring Research Institute has been in business since 1996 and just wrapped up a new expansion project. |
By Annalee Armstrong Exicure has already cut its workforce to the bone, but now the nucleic acid therapy biotech is searching for some sort of transaction to save what’s left of the company |
By Annalee Armstrong Silence Therapeutics is snatching back two siRNA drug targets developed through a $20 million collaboration with Mallinckrodt Pharmaceuticals. |
By Max Bayer Sonoma Biotherapeutics is making waves more than a year and a half after securing one of the largest fundraising rounds of 2021. The biotech is announcing a new collaboration with Regeneron worth up to $120 million. |
By James Waldron With its lead chronic pouchitis treatment stuck in limbo as the company searches for a phase 3 partner, it looks like Applied Molecular Transport has finally thrown in the towel. |
By Annalee Armstrong Things must be going well for Bristol Myers Squibb’s legacy Celgene-Evotec neurodegeneration partnership. The New York Big Pharma has decided to add another eight years to their agreement, boosting the overall potential deal value to $4 billion. |
By Nick Paul Taylor Boehringer Ingelheim has spied an opportunity to seize the holy grail of immuno-oncology: turning cold tumors hot. In return for $10 million upfront and up to $471 million milestones, the German drugmaker has tasked Covant Therapeutics with discovering covalent candidates against an emerging cancer target. |
By Max Bayer Monopar Therapeutics is moving on from a treatment for chemotherapy side effects after disappointing phase 2 data left the company empty-handed. |
By Paige Minemyer NASHVILLE—Innovation in healthcare is notoriously slow, and UnitedHealth's Sandeep Dadlani is aiming to pick up that pace. |
By Angus Liu Rare diseases and cancer are constantly featured in the biopharma M&A landscape. Now, one biotech company with a presence in both areas has reportedly caught Big Pharma’s interest. |
By Andrea Park For the first time in at least a decade, the head of Johnson & Johnson’s medtech division is among the company’s highest-paid executives. |
By Fraiser Kansteiner Amicus Therapeutics' Pombiliti—which combines a long-term enzyme replacement therapy with the oral enzyme stabilizer miglustat—has been approved by the European Commission as Pombiliti in adults with late-onset Pompe disease. Now, the company must wait on the European Medicines Agency’s Committee for Medicine Products for Human Use to deliver a verdict on miglustat specifically. |
By Dave Muoio Hospital IT and medical device company leaders say that many organizations have no choice but to adopt a "grow-your-own" approach to data privacy and security workforce vacancies. |
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 |
Whitepaper This paper describes the key elements of good US/EU corporate governance for US-based biopharma companies in operating Europe. Sponsored by: Blue Matter, strategic consultants in the life sciences |
Executive Summary Read about the latest survey results from over 200 biopharma executives and the changing approaches to building biologic drug development pipelines. Sponsored by: Twist Bioscience |
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Whitepaper What are key considerations for intranasal delivery in the treatment of acute and chronic conditions? Sponsored By: Catalent |
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 |
Whitepaper As sponsors increasingly look to CROs to support their clinical studies, making and addressing certain clinical supply considerations at the outset of the relationship can reduce the risk of potentially unforeseen impact to budget and time later. Discover key issues sponsors should consider to help their CRO or partner of choice better understand their clinical supply needs. Sponsored by: Catalent |
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 |
Whitepaper Learn how Catalent’s extensive network across APAC can meet a wide range of clinical supply needs for sponsors conducting trials within the region. Sponsored by: Catalent |
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Research Learn more on an approach for process characterization for the production of a monoclonal antibody, which will improve the efficiency and effectiveness of the process by targeting the right design and number of experiments. Sponsored by: Catalent |
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Whitepaper Planning on using a CRO to support your next clinical study? This infographic outlines critical areas to address at the start of the relationship in order to ensure that budget and timelines keep on track for the duration of the trial. Sponsored by: Catalent |
Case Study Learn more on an approach for process characterization for the production of a monoclonal antibody, which will improve the efficiency and effectiveness of the process by targeting the right design and number of experiments. Sponsored by: Catalent |
| May 1-3, 2023 | Jersey City, NJ |
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