CureVac giving up on first COVID mRNA vax, focusing on GSK-partnered 2nd attempt J&J science chief Stoffels to retire after decade at the top, adding to C-suite changes Billions club: Takeda taps Poseida for 2nd $1B-plus gene therapy pact in 2 weeks Sponsored: Purify DNA, RNA, proteins, and cells for many applications Boston biotech backers quit Dana-Farber board after U-turn on investment policy: report Sponsored: Partnership to unlock the full potential of data to advance the science and practice of healthcare: Q&A with Syntropy and the University of California, Irvine Gossamer unveils new pipeline plans a year after lead program fizzled out in phase 2 Roche's Spark adds epilepsy asset to pipeline with $328M CombiGene licensing deal Veracyte kicks off limited release of its nasal swab lung cancer test as it gears up for full commercial launch Eyes itching from allergies? Ocular's Dextenza wins FDA approval as first monthly implant Kaiser Family Foundation: Public not buying pharma's arguments over drug price reforms Featured Story By Ben Adams With more than a touch of inevitability, CureVac is abandoning its first mRNA COVID vaccine after dismal results earlier this year, and switching focus to its second mRNA asset with GlaxoSmithKline. read more |
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| Top Stories By Nick Paul Taylor Johnson & Johnson Chief Scientific Officer Paul Stoffels is to retire at the end of the year, ending a nine-year stint at the top of the rejuvenated R&D unit and creating more turnover at the top of the Big Pharma. read more By Kyle LaHucik Last week it was Selecta Biosciences. This week, Takeda's gene therapy investment push is helping lift Poseida in a potentially $3.6 billion research collaboration and licensing deal that will give the Japanese Big Pharma access to up to eight non-viral gene therapies for liver and hematologic diseases. read more Sponsored by: Thermo Fisher Scientific Discover ways your Thermo Scientific™ KingFisher™ system can empower your research beyond SARS-CoV-2. read more By Nick Paul Taylor Dana-Farber Cancer Institute has reportedly barred trustees from newly investing in biotechs created to license its science, leading to the resignation of board members including a co-founder of C4 Therapeutics. read more Sponsored by: Syntropy Q&A with Syntropy and UCI on their collaboration to work across their enterprise and with external partners to advance health research and patient care. read more By Annalee Armstrong Almost a year to the day after Gossamer Bio’s lead program failed twice in phase 2, the California biotech is unveiling two preclinical assets ready to enter the clinic in an effort to turn things around. read more By Annalee Armstrong Roche’s Spark Therapeutics unit is offering up to $328.5 million in biobucks for CombiGene’s gene therapy for epilepsy, which has a specific focus on drug-resistant forms of the condition. read more By Conor Hale The company also delivered recent findings that showed the Percepta genomic test’s ability to more accurately separate groups of patients based on their risk of developing tumors from suspicious lung nodules. read more By Angus Liu Patients with itchy eyes caused by allergic inflammation often take eye drops multiple times per day. Thanks to an FDA approval, a monthly insert into the canaliculus of the eye will soon be available. read more By Robert King A new poll finds that a large swath of the public aren't buying the pharmaceutical industry's arguments against giving Medicare drug price negotiation authority. read more Resources Sponsored By: Unlearn AI Read Unlearn’s whitepaper to learn about how novel trial designs with Digital Twins enable more efficient clinical trials, with higher power and smaller required sample sizes. Sponsored By: Trial Interactive Check out the eTMF Implementation Quick Guide to see a checklist TMF experts developed to help you reduce risks, maintain compliance, and establish effective processes in your eTMF. Sponsored By: Bioclinica This whitepaper addresses where AI can make the biggest impact in clinical trials. Sponsored by: Thermo Fisher Scientific Looking to accelerate your biotech company, but not sure where to start? 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Virtual U.S. Healthcare Compliance Certificate Program October 11 – 14, 2021 Fierce Biotech Cell & Gene Therapy October 19, 2021 | Virtual Event Learn what it takes to get a drug developed and approved October 20-21, 2021 | Live & Online Fierce Health Payer Summit October 26, 2021 | Virtual Event Pharma Meeting Pros Summit November 3-4, 2021 | Atlantic City, NJ & Virtual Learn how to develop and get regulatory approval for medical devices November 3-4, 2021 | Live & Online Diversity, Equity & Inclusion Summit November 9–10, 2021 | Virtual Event Drug Development Boot Camp® 2021 Onsite and VIRTUAL in real time November 17-18, 2021 | Register now! Pre-Boot Camp preparation is now available. Learn impact of pricing, competitive assessment, epidemiology November 17-18, 2021 | Live & Online Learn how therapeutics are successfully launched and commercialized December 1-2, 2021 | Live & Online Fierce Biotech Forum 2022 | Virtual Event |