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Featured Story | By Nick Paul Taylor Kumquat Biosciences may have said little publicly about its anticancer small molecule platform, but it has caught the eye of Eli Lilly. Committing to more than $2 billion in milestones to join forces with the Roche-backed biotech, Lilly is handing over $70 million upfront. read more |
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Top Stories By Ben Adams Questions abound over the future of GlaxoSmithKline’s chief Emma Walmsley but its research platform, which recently lost a key player and has been beset by flops and failures of late, may be in more urgent need of attention. That, however, isn’t in the cards. read more By Ben Adams Sanofi has made a small trim to its pipeline today, though its near-term R&D focus remains on the 35,000-strong COVID vaccine test it started last quarter. read more Sponsored By: Clever Leaves Medical cannabis from Colombia can change lives. read more By Nick Paul Taylor It's official. Regeneron and Sanofi need not be concerned about Dupixent competition from tezepelumab for the skin condition called atopic dermatitis. Dupixent's asthma franchise, though, is still in AstraZeneca's sight. read more By Amirah Al Idrus After taking aim at the customary $100 million IPO, Nuvalent is reeling in $166 million to propel a pair of lung cancer treatments into and through the clinic. The IPO comes just six months after the cancer biotech emerged from stealth with $50 million and two months after it added another $135 million to the bank. read more By Kyle LaHucik,Annalee Armstrong Annovis Bio wants its therapy to be better than Biogen's Aduhelm, but the latest data shows the drug did not improve dementia symptoms, problem-solving, orientation or judgment, among other data points. The company revealed a mixed—and confusing—bag of results from a small phase 2a study Wednesday night at the 2021 Alzheimer's Association International Conference in Denver. read more By Amirah Al Idrus After filing to raise up to $100 million in its Wall Street debut, Rallybio is reeling in a smaller sum of $80.6 million. The funds will bankroll several clinical trials, including a phase 1/2 study of its lead asset in a rare fetal bleeding disorder. read more By Kyle LaHucik Ten months after securing its first drug approval for head and neck cancer in Japan, Rakuten Medical has picked up another megaround of financing, in the form of a $166 million series D, to expand into new therapies and indications. The San Mateo, California-based company said Thursday the series D translates to $75 million in new capital and $91 million converted promissory notes. read more By Kyle LaHucik The compound farnesol, found in berries and other fruits, could inspire new Parkinson's disease treatments, Johns Hopkins researchers said. In mouse studies, the team found that it prevented the loss of dopamine neurons and reversed symptoms of the disease. read more By Beth Snyder Bulik Finding clinical trial results for a specific drug can be challenging—but reading through them can be even more daunting. Pfizer and other pharmas are expanding efforts to publish study summaries in everyday language to make them easier to understand and comply with EMA rules that kick in next year. read more By Beth Snyder Bulik An advocacy group says Johnson & Johnson has yet to make things right with Black women after years of targeted talc powder advertising—so it's suing. The National Council of Negro Women this week asked the courts to force J&J to create equally targeted “corrective marketing” and fund outreach efforts to Black women and their families. read more By Robert King A bipartisan Senate infrastructure deal will not rely on unspent COVID-19 relief funds as a pay-for, but it will delay the controversial rebate rule. read more By Conor Hale After raising just $40 million less than a year ago, Exo has secured another $220 million as investors line up to back the company's point-of-care diagnostic device. read more Resources Sponsored by: Box Read Get to Know Cloud Content Management for Life Sciences and learn how to eliminate silos across all workflows, from R&D to commercialization. Sponsored by: Evidera, a PDD business Learn about key post-marketing safety study solutions, including registries and REMS, and how they can most effectively help meet regulatory requirements and maximize patient access. Sponsored by: WCG Engage Independent Expert Endpoint Adjudication and Data Monitoring Committees in a strategic manner to identify methods for retrospective and prospective evaluations that may improve competitive advantage and bolster regulatory submissions. Sponsored by: Patheon by Thermo Fisher Scientific Take a closer look at your supply chain to ensure it delivers with speed, efficiency, and quality — all within budget. Sponsored by: Patheon by Thermo Fisher Scientific Choose the right AAV platform for your viral vector-based therapy Sponsored by: Blue Matter Consulting E-book to get newcomers “up to speed” quickly on digital health and digital therapeutics while also addressing key issues important to those already familiar with the topic. 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