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BioWorld - Wednesday, February 18, 2026
Home » Topics » Medical technology, Clinical

Medical technology, Clinical
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FDA lays framework for engaging patients in device clinical trials

Sep. 24, 2019
By Meg Bryant
BOSTON – The FDA's Center for Device and Radiological Health (CDRH) released draft guidance on Monday aimed at encouraging the use of patient input in medical device clinical trials and helping sponsors understand how they can use patient engagement to improve the design and conduct of investigations.
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Prosthetic leg restores sensations, eases patient phantom pain

Sep. 13, 2019
By Nuala Moran

Product clinical data for Sept. 12, 2019

Sep. 13, 2019

Product clinical data for Sept. 11, 2019

Sep. 12, 2019

Study finds PGDx liquid biopsy detects biomarker to predict checkpoint inhibitor response

Sep. 12, 2019
By Stacy Lawrence
There have been three oncology drug approvals by the U.S. FDA over the last few years that were based solely on a genetic biomarker, rather than the location in the body where the tumor originated. But to make this tissue-agnostic approach a reality for oncology patients, detecting those genetic biomarkers will have to become increasingly easy and standardized.
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Oncimmune test identifies lung cancer four years earlier than CT screening alone

Sep. 12, 2019
By Annette Boyle

Abbott's Tendyne scores well in trial of patients with severe calcification

Sep. 11, 2019
By Mark McCarty
The recent progress in interventional cardiology has largely been driven by the aortic valve, although calcification of the aortic root has proven a difficult hurdle to overcome. A newly published study demonstrates that the Tendyne device by Abbott Vascular Inc., of Santa Clara, Calif., can be readily used not just to treat failing mitral valves, but works well in these patients with severe calcification, an achievement that could quickly vault the transcatheter approach past conventional surgical approaches in this population.
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Product clinical data for Sept. 6, 2019

Sep. 9, 2019

Abbott launches IDE trial of leaky tricuspid heart valve technique

Sep. 6, 2019
By Meg Bryant
Abbott Laboratories has kicked off a pivotal study to evaluate its catheter-based Triclip transcatheter tricuspid valve repair system in patients with severe tricuspid regurgitation (TR). The first enrollments in the U.S. FDA-approved Triluminate study were performed at Abbott Northwestern Hospital in Minneapolis by a cardiac team led by Paul Sorajja, director of the Center for Valve and Structural Heart Disease at the Minneapolis Heart Institute and co-primary investigator for the trial.
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No Pfizer common divisor in DMD; tox woe bestows 'Solid' favor on Sarepta

July 29, 2019
By Randy Osborne
In late June, when Pfizer Inc. unveiled the first phase Ib data, mixed safety signal and all, for its Duchenne muscular dystrophy (DMD) gene therapy, PF-06939926, investors in Sarepta Therapeutics Inc. as well as Solid Biosciences Inc. watched with particular interest. The latter firm seems none the worse for wear, though, raising $60 million in a private placement.
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