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BioWorld - Thursday, April 23, 2026
Home » Topics » Clinical

Clinical
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Analysis appears to take some of the heat off paclitaxel-eluting stents, DCBs

Oct. 10, 2019
By Nuala Moran
LONDON – There is no evidence for increased mortality in patients receiving paclitaxel-eluting stents and drug-coated balloons (DCBs) to treat peripheral arterial disease, according to the largest real-world safety analysis to date. The findings may come as a relief to many, particularly after a meta-analysis published in December 2018 led to safety warnings and restrictions on the use of coated and drug-eluting devices.
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Chi-Med gears up for China NDA after surufatinib hits phase III endpoint in NET

Oct. 9, 2019
By David Ho
HONG KONG – Hutchison China Meditech Ltd.'s (Chi-Med) is preparing for the next step after surufatinib achieved its primary endpoint in a phase III SANET-ep study in extra-pancreatic advanced neuroendocrine tumors (NETs) in China.
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Merck's Recarbrio, Shionogi's cefiderocol tackle bacterial pneumonia in phase III studies

Oct. 9, 2019
By Michael Fitzhugh
WASHINGTON – Hot on the heels of July's FDA approval of Recarbrio (imipenem, cilastatin and relebactam) in complicated urinary tract infections (cUTIs), Merck & Co. Inc. rolled out pivotal phase III data at the Infectious Disease Society of America's IDWeek 2019 that could support expanding its label to another high-need group, people with hospital-acquired or ventilator-associated bacterial pneumonia (HABP/VABP).
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Gene-eye out of the bottle: Adverum, Regenxbio bids to yield AMD data shortly

Oct. 9, 2019
By Randy Osborne
Something of a duel may be shaping up between Menlo Park, Calif.-based Adverum Biotechnologies Inc. with ADVM-022, the phase I gene therapy candidate for wet age-related macular degeneration (AMD) and Regenxbio Inc., of Rockville, Md., with a similar candidate.
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Neuronetics unveils largest major depression registry study results, as it eyes PTSD

Oct. 8, 2019
By Stacy Lawrence
The routine application of medical device technology to neurological indications beyond pain remains challenging in all but the most severe patients. Micro-cap Neuronetics Inc. is aiming to change all that with its Neurostar transcranial magnetic stimulation (TMS) system that is noninvasive and used in the physician's office.
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Three win Nobel prize for their hypoxia work

Oct. 8, 2019
By Anette Breindl
William Kaelin, Peter Ratcliffe, and Gregg Semenza have jointly won the 2019 Nobel Prize "for their discoveries of how cells sense oxygen," the Nobel Assembly at Karolinska Institutet announced today.
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Good, better, best? Street can't let it rest; NGM data in NASH keeping to trend

Oct. 8, 2019
By Randy Osborne
Investors sorting through NGM Biopharmaceuticals Inc.'s interim results from the fourth and final cohort of the adaptive phase II trial with aldafermin in nonalcoholic steatohepatitis (NASH) may have felt let down when comparing the data to previous cohorts' outcomes. Shares of the South San Francisco-based firm (NASDAQ:NGM) closed Monday at $10.78, having sunk $2.77 or 20.4%.
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Pfizer aspires to be first with universal maternal RSV vaccine

Oct. 8, 2019
By Michael Fitzhugh
WASHINGTON – While the vast majority of people infected with respiratory syncytial virus (RSV) muddle through with mild, cold-like symptoms, for infants, the associated bronchiolitis can make it extremely difficult to breathe and feed. Thousands require inpatient care for the infection each year, necessitating hospitals to be built with a winter surge of admissions in mind, driven in large part by RSV in both the very young and old.
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Researchers test the first neuroprosthetic leg, now aim for a larger, longer study

Oct. 4, 2019
By Stacy Lawrence
Arm and hand prosthetics have long been the focus for researchers aiming to offer sensation as well as more precise and easily controlled movement by connecting patient nerves to sensors in the prosthetic. But now that effort has been extended to leg prosthetics as well.
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Merck's Recarbrio, Shionogi's cefiderocol tackle bacterial pneumonia in phase III studies

Oct. 3, 2019
By Michael Fitzhugh
WASHINGTON – Hot on the heels of July's FDA approval of Recarbrio (imipenem, cilastatin and relebactam) in complicated urinary tract infections (cUTIs), Merck & Co. Inc. rolled out pivotal phase III data at the Infectious Disease Society of America's IDWeek 2019 that could support expanding its label to another high-need group, people with hospital-acquired or ventilator-associated bacterial pneumonia (HABP/VABP). Shionogi & Co. Ltd., which is advancing its investigational antibiotic, cefiderocol, in the same indications, also shared new phase III data supporting its use in the high-risk population.
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