- Coya Therapeutics Presents Updated ALS Biomarker Data at the 2nd Annual Johnson Center Symposium
- Hyundai Bioscience Announces Clinical Development Plan for Niclosamide-based Metabolic Anticancer Drug Targeting P53 Mutation Cancer
- Sedana Medical Completes Patient Recruitment for INSPiRE-ICU 1 Clinical Trial in the US
- How Nefab’s Sustainable Packaging and Logistics Solutions Revolutionize the Healthcare Equipment Industry Supply Chain | By Lise-Anais Swiegot, Global Healthcare Segment Director with the Nefab Group
- Discover Reeva FT: Revolutionizing Wound Covering for Healthcare Pros
- Medical Grade, Premium Standing Solutions Drastically Improve Employee Comfort, Support, Productivity and Morale While Reducing Fatigue, Stress and Ailments | By Amy Hester, PhD, RN, BC, FAAN, Chairwoman and CEO, HD Nursing, & Daniel Bouzide, Founder and President, WellnessMats
- Unlocking New Hope: Alzheimer’s Patients Join Amyloid-Targeting Therapy Study
Medical Device News Magazine delivers the latest updates from the medical device and biotechnology sectors.
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Medical Device Industry News: Latest Developments, Breakthroughs, and Future Outlook
Clinical Trials
iRhythm Technologies: Study Published in JAMA Cardiology Finds Zio by iRhythm Proactively Identifies AFib, Increases Detection Tenfold
iRhythm Technologies advises the transatlantic clinical trial found that Zio by iRhythm, an ambulatory cardiac monitoring solution, led to a tenfold increase in the detection of atrial fibrillation (AF) versus patients receiving standard clinical care.
Cerapedics Completes Enrollment of Pivotal U.S. FDA IDE Study for its P-15L Bone Graft
Cerapedics notes results from the study are intended to be used in a Premarket Approval (PMA) submission to the FDA.
PolyActiva Announces Positive Phase IIa Trial Results in Low Dose Cohort for PA5108 Ocular Implant with Prezia™ Sustained Drug Delivery Technology
The open-label, multicenter, Phase IIa study was designed to evaluate the minimum effective dose of the PA5108 Ocular Implant in patients with mild to moderate POAG across 3 dose cohorts (10 subjects per cohort). Primary and secondary efficacy endpoints include mean diurnal IOP at 12 and 26 weeks compared to baseline, and 8am IOP at 6, 18 and 21 weeks compared to baseline.
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