| Taking the Fight to Rare Cancers Beating rare cancers demands expertise in oncology and rare diseases. Our white paper shows how adaptive design, study committees, and cross-industry cooperation are fueling real progress. Premier Research. Built for Biotech℠ | Today's Rundown Chasing AbbVie, Gilead files for approval of filgotinib in Japan Chinese infectious disease biotech Ascletis nabs Novartis exec as CSO Cygnal officially uncloaks with $65M and exoneural approach to cancer [Sponsored] Thwarting Subjectivity in Clinical Trials Novartis' Xolair follow-up banishes hives in 42% of patients with chronic hives Merck taps 4D pharma for bacterial vaccine R&D project Novartis takes on Regeneron, Roche blockbusters with Beovu approval Featured Story | Tuesday, October 8, 2019 Gilead Sciences has filed for approval of JAK1 inhibitor filgotinib in Japan. The submission moves Gilead a step closer to selling the Galapagos-partnered drug to rheumatoid arthritis patients in the country. |
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| Top Stories Tuesday, October 8, 2019 After poaching an ex-Merck exec to run its R&D, Chinese biotech Ascletis has raided another U.S. Big Pharma for its new chief scientific officer. Tuesday, October 8, 2019 When Roche veteran Pearl Huang landed at Cygnal Therapeutics in January, the company painted a broad picture of its exoneural approach to treating cancer. Now, as Flagship Pioneering officially launches Cygnal, the startup is filling in some details. Monday, October 7, 2019 A clinical trial is a measurement system, but too often, we fail to calibrate the most significant of measurement instruments: trial participants. Tuesday, October 8, 2019 Two doses of Novartis’ new treatment for chronic hives cleared the skin of more patients than Xolair, its Roche-partnered asthma drug. The highest dose of the drug banished hives in 51% of patients, compared to 26% of patients taking Xolair. Tuesday, October 8, 2019 Merck has teamed up with 4D pharma to develop bacterial strains as vaccines. The deal gives Merck the chance to pick up three candidates against undisclosed indications for an upfront fee and up to $347.5 million (€316.2 million) in milestones. Tuesday, October 8, 2019 Novartis has its next big drug approval. The FDA on Tuesday approved wet AMD drug Beovu, which will go up against entrenched blockbusters Eylea from Regeneron and Lucentis from Roche. The drug has shown it can match up against Eylea's efficacy and bested the Regeneron drug on other measures. Resources Sponsored by: Medidata Simplified filing, improved oversight, audit readiness: is your eTMF system delivering best-in-class benefits? Sponsored by: Colorcon® Learn about how you better manage product authentication and battle drug counterfeiting with innovative solutions. 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BioBasics: Biotech For The Non-Scientist Oct 22-23, 2019 | San Diego, CA BioImmersion: Biotech for the Non-Scientist October 23-25, 2019 | Chicago, IL 4th FierceBiotech Drug Development Forum October 28-29, 2019 | Boston, MA Drug Development Immersion November 7-8, 2019 | Boston, MA Advanced Therapies: Immunotherapies, Cell Therapies and Gene Therapies November 15, 2019 | Boston, MA Countdown to Drug Development Boot Camp® 2019 November 20-21, 2019 | Boston, MA | Register Now at www.drugstomarket.com/drugbootcamp and start Pre-Boot Camp Preparation |