Medical device company Empatica said on Friday that it will supply its wearable plus algorithm for the early and presymptomatic detection of COVID-19 to the US Army Medical Research and Development Command (USAMRDC) under a partnership between the parties.
According to the company, the aura algorithm delivers the risk indication of a person suffering from COVID-19 on a daily basis using physiological data read by its medical smartwatch, EmbracePlus. The focus is preventing outbreaks through early detection and warning. The wearable and algorithm will detect COVID-19 and alert individuals of the potential presence of an infection.
The USAMRDC project is divided into several phases and starts with the clinical validation of the the company's algorithm in healthy participants at risk of developing SARS-CoV-2. The approval will be submitted to the US FDA and the project will end in a virtual clinical trial with participants ready to test and validate the entire platform.
In addition, the company's EmbracePlus is a medical device in a smartwatch form factor, with highly sensitive sensors that measure heart rate, heart rate variability, temperature, respiratory rate and electrodermal activity. The device monitors a person's vital functions and sends application-internal warning messages in the event of patterns that indicate a COVID-19 infection, allowing self-isolation.
Hyphens Pharma licenses Cerapro skin cream to Louis Widmer for six European markets
Profusa signs French distributor to expand Lumee Oxygen rollout in Europe
Sensiva Health names new chief operating officer
BrioHealth Solutions enrols 100th participant in BrioVAD System trial
Abbott's Amplatzer Piccolo Delivery System receives US FDA clearance and CE Mark
Amphix Bio announces initial closing of USD12.5m seed financing round
Bioretec wins FDA breakthrough status for biodegradable orthopaedic DrillPin
Amferia raises EUR3.5m to advance antimicrobial wound-care platform
BioCryst wins FDA approval for oral HAE prophylaxis in young children
ALR Technologies announces GluCurve Pet CGM relaunch in Canada
Galderma secures EU MDR certification for Sculptra, expanding use to multiple body areas
Clinical Laserthermia Systems applies for CE marking of ClearPoint Prism neuro laser system
Bonesupport shifts CERAMENT V review to FDA's De Novo pathway
Neola Medical secures US patent for disposable lung monitoring probes