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BioWorld - Saturday, December 27, 2025
Home » Topics » Clinical

Clinical
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Three late-stage drugs look to battle in Cushing's syndrome market

Oct. 2, 2019
By Brian Orelli
The Cushing's syndrome market is heating up with three second-generation drugs in late-stage development to join the two approved medications, Signifor (pasireotide, Recordati SpA) and Korlym (mifepristone, Corcept Therapeutics Inc.), as well as a couple of off-label options.
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Study finds Orchestra Biomed's Backbeat device reduces hypertension

Oct. 1, 2019
By Stacy Lawrence

Intact's vascular scaffold hits endpoints in above-the-knee European study

Oct. 1, 2019
By Meg Bryant

Abbott unveils positive data on Mitraclip, Triclip

Oct. 1, 2019
By Liz Hollis
Abbott Laboratories had a busy Transcatheter Cardiovascular Therapeutics (TCT) 2019 conference. Among the news it generated was the unveiling of new analyses of the COAPT trial on the cost-effectiveness of Mitraclip vs. guideline-directed medical therapy (GDMT) alone in heart failure patients with secondary mitral regurgitation (MR).
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Leave that apabetalone? Resverlogix: Please stay for AHA six weeks away

Oct. 1, 2019
By Randy Osborne
Wall Street will have to wait until the American Heart Association (AHA) meeting next month in Philadelphia for full data from Resverlogix Inc.'s phase III BETonMACE trial with apabetalone, but disclosure of the endpoint miss was enough to send investors fleeing.
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Seagen shares rise on phase I urothelial cancer data

Oct. 1, 2019
By Michael Fitzhugh
Shares of Seattle Genetics Inc. (NASDAQ:SGEN) rose 12.4% to $85.40 on news that an antibody-drug conjugate (ADC) it is developing with Tokyo-based Astellas Pharma Inc., when combined with Keytruda (pembrolizumab, Merck & Co. Inc.), shrank tumors in the majority of people participating in a phase I first-line bladder cancer study.
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Abbott's pivotal trial results for Portico boosted by new delivery system

Sep. 30, 2019
By Stacy Lawrence
SAN FRANCISCO – Abbott Laboratories expects that its self-expanding transcatheter aortic valve replacement (TAVR) system Portico will be able to become a top competitive product. A pivotal trial of Portico has found that the implant is noninferior to current FDA-approved TAVR systems that are marketed in the U.S. The results from the 750-patient, randomized trial were presented here last week at the Transcatheter Cardiovascular Therapeutics (TCT) conference.
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Investigator-led study finds BSX's Acurate Neo not noninferior vs. Edwards' Sapien 3

Sep. 30, 2019
By Stacy Lawrence
SAN FRANCISCO – As the transcatheter aortic valve replacement (TAVR) field matures, it is becoming increasingly difficult to develop a new implant that can distinguish itself vs. competitors. The incremental benefits are narrowing rapidly, making it tough to distinguish new iterations from one another using standard, randomized trials.
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Medtronic gets greenlight for Intrepid TMVR study with transfemoral approach

Sep. 30, 2019
By Meg Bryant

Ancora Heart sees positive early results with Accucinch in systolic heart failure

Sep. 30, 2019
By Liz Hollis
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