| |
With the emergence of precision medicine and its focus on customizing treatment to individual patients, it may be possible to reduce the time to diagnosis for rare conditions, enabling identification and intervention at earlier stages of the disease – a hope that is new for rare disease patients. Explore this and more in our latest blog. .png)
|
|
Today's Big NewsMar 21, 2023 |
| By Annalee Armstrong $100 million for Rapport Therapeutics. $112 million for Noema Pharma. $108 million for Bicara Therapeutics. The megaround has come roaring back in the past few weeks, but is biotech really healing? |
|
|
|
By Max Bayer For a moment there, it seemed as though a reverse merger between Carisma Therapeutics and Sesen Bio was on thin ice. Activist investors at the latter were holding up the marriage, largely to maximize the amount of cash that would be dispersed to Sesen shareholders. But after months of negotiating, the final assuaging came from Carisma’s head honcho. |
By Nick Paul Taylor Evofem Biosciences is making top-to-bottom cuts in a bid to slash its costs. Months after laying off 39 people, the women’s health biotech has pushed more employees, including its chief commercial officer, out the door and cut the salary of its CEO by 40%. |
Sponsored by DrugBank Data rich but quality poor. Massive amounts of disorganized data might be the final roadblock to unlocking the potential of data-centric AI. |
By Nick Paul Taylor Selecta Biosciences and Sobi have laid down a marker in their attempt to challenge Horizon for the gout market, delivering phase 3 data that suggest their SEL-212 candidate can match the efficacy of Krystexxa despite being administered less frequently. |
By Max Bayer Gilead has selected the first fruit borne from a 2019 collaboration with Nurix, taking on an IRAK4 degraded to tackle inflammatory diseases. Gilead is paying up to $445 million to exclusively license the med. |
By Helen Floersh Swiss bioengineering firm Cutiss has launched skin cell experiments to the International Space Station. The artificial skin maker hopes to learn how microgravity impacts wound healing, with implications for future research and, maybe someday, its product pipeline. |
By Andrea Park During a hearing that lasted just under 90 minutes on Friday, Judge Edward Davila stopped short of offering a definitive ruling on Elizabeth Holmes' dual bids to stay out of prison while awaiting an appeal and to avoid paying restitution for her four felony convictions. |
By Joseph Keenan Clario, a Philadelphia-based clinical health tech company, is partnering with Strados Labs to use its FDA-approved respiratory monitoring device for clinical trials. |
By Zoey Becker While UCB waits for the FDA's approval decision on bimekizumab in psoriasis, the company is touting new data in another indication. The company presented 48-week data in hidradenitis suppurativa at the American Academy of Dermatology's 2023 meeting. |
By Robert King States should have the power to restrict Medicaid coverage of drugs cleared via the FDA's accelerated approval pathway just like in Medicare, a new MACPAC report said. |
Fierce podcasts Don't miss an episode |
| This week on "The Top Line," we discuss the SVB failure, what to expect next and what it all meant for the biotech industry. We also cover Pfizer's big acquisition, insulin prices and more of this week's top headlines. |
|
|---|
|
|
|
May 1 - 3, 2023 | Jersey City, NJ Don’t miss the opportunity to gain best practices in medical affairs strategy development and ensuring scientific materials are created and shared in a regulatory compliant manner to internal/external stakeholders and thought leaders. Register Today & save $200 from now until April 7th! .png)
|
|
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 |
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 |
Whitepaper Have you had your questions about mRNA/saRNA manufacturing unanswered during a webinar; have no fear, we have you covered here. Sponsored by: Aldevron |
Whitepaper Download Herspiegel Consulting’s Go-To-Market Model, based on 100+ launches, to learn the critical components, and timelines for commercial success. Sponsored by: Herspiegel Consulting |
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 |
Whitepaper Discover key considerations that every trial sponsor should know when navigating the complex clinical supply distribution landscape across Asia-Pacific. Sponsored by: Catalent |
Whitepaper How can specialized expertise help you optimize your clinical supply chain? Learn about the roles and responsibilities of unique experts such as clinical supply management, project management, and financial project analysis. Sponsored by: Catalent Clinical Supply |
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 |
Whitepaper Explore Catalent’s newest clinical supply facility in Japan, including the comprehensive services & solutions it offers to help support trials both in-country & around the world. Sponsored by: Catalent |
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 |
|
|
| |
|
