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Significant patient populations, top clinical institutions, and ease of
regulatory compliance combined to support oncology trial success in APAC. Download our white paper to explore the growth of oncology trials in APAC countries and strategies to support global study success in this dynamic and complex region. Premier Research. Built for Biotech℠ 
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Today's Big NewsOct 28, 2022 |
| By Nick Paul Taylor The dream of taming IL-2 keeps slipping further away. After seeing Bristol Myers Squibb and Nektar Therapeutics give up on their candidate, Sanofi has reported “lower than projected” efficacy data on its prospect and rethought its plans for the molecule. |
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By Nick Paul Taylor Vultures are circling Quantum Genomics. A high-stakes phase 3 hypertension readout has gone against the French biotech, prompting it to stop work on firibastat in cardiology and reallocate its remaining 11 million euros ($11 million) to other projects. |
By Max Bayer A new STAT News investigation has found that Eisai's experimental Alzheimer's drug lecenemab may have contributed to a patient's death, according to documents obtained by the outlet. The Japanese pharma acknowledged the death but wouldn't divulge specific details citing patient privacy. |
By Gabrielle Masson An increasingly bitter conflict between biotech and investor has come to a close, with Mereo BioPharma losing out to Rubric Capital Management and handing the activist investor four spots on its board. |
By Helen Floersh Evidence is growing that insulin resistance drives Alzheimer’s development, and several medications used to treat diabetes are in clinical trials to see if they can combat the condition. Now, new findings about the way insulin is delivered to the brain suggest that it’s worth looking into a broader range of diabetes drugs than previously thought. |
By Querida Anderson This week on “The Top Line,” we dig into rumors of a shaky relationship between Biogen and Eisai. We also chat about AZ’s ability to finally tout the approval of an asset that’s seen many failures over the years. |
By Max Bayer,Gabrielle Masson Frazier is leaving Merck after 30 years, handing the executive chairman role to CEO Davis. GSK's vaccine chief is departing amid a restructuring of the medicine and vaccine units. CRISPR development head Klein leaves as the company nears its first regulatory filing. |
By Andrea Park Months after its G7 continuous glucose monitor landed European approval in March—leading to a wide-scale rollout of the sensor across the continent earlier this month—Dexcom is zeroing in on the U.S. market. |
By Angus Liu Over a year after the FDA’s dreaded boxed warning addition and treatment line demotion, the JAK inhibitor class of inflammatory disease drugs has gotten its uses restricted by European regulators as well out of safety concerns. |
By Dave Muoio CMS said it was loosening vaccination requirements and noncompliance citation severity for certain healthcare facilities due to "relatively low" COVID-19 hospitalizations and deaths across the nation. |
By Ben Adams Endo has certainly captured the public's imagination with its Peyronie's disease (PD) campaigns before—think wonky veg—but this time, it’s playing it straight. |
By Angus Liu Sumitomo has persuaded Myovant into an acquisition that values the latter at $2.9 billion. Astellas is doubling down in gene therapy with a $50 million investment in Taysha Gene Therapies. A couple in a trade secret theft case involving Roche's Genentech and Taiwanese firm JHL Biotech have received six months in prison. And more. |
Fierce podcasts Don't miss an episode |
| This week on “The Top Line,” we dig into rumors of a shaky relationship between Biogen and Eisai. We also chat about AZ’s ability to finally tout the approval of an asset that’s seen many failures over the years. |
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Wednesday, November 2, 2022 | 1pm ET / 10am PT This webinar will discuss how Invitae and others are working together to characterize the lived experience of patients with rare bile duct cancer, and ultimately, improve patient care. Register now. 
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