Novocure’s Optune Gio fails to show benefit at earlier stage
Novocure’s stock has dropped more than 15% after its Phase III glioblastoma study of Optune Gio failed to show benefit …
Novocure’s stock has dropped more than 15% after its Phase III glioblastoma study of Optune Gio failed to show benefit …
FiberSense has obtained a CE mark for its continuous glucose monitoring (CGM) system, setting the stage for the medical device’s …
In January 2026, the American Heart and American Stroke Association (AHA/ASA) issued new care guidelines for acute ischemic stroke (AIS) …
The government of Japan has inducted Sonire Therapeutics’ Japan-based group into an innovation programme, along with equipping the company with …
Australian healthcare company BCAL Diagnostics is developing the BREASTEST Monitor blood test intended to assist in evaluating women for local …
In January 2026, the American Heart and American Stroke Association (AHA/ASA) issued new care guidelines for acute ischemic stroke (AIS) …
The government of Japan has inducted Sonire Therapeutics’ Japan-based group into an innovation programme, along with equipping the company with …
Australian healthcare company BCAL Diagnostics is developing the BREASTEST Monitor blood test intended to assist in evaluating women for local …
AngioDynamics has received approval from the US Food and Drug Administration (FDA) for an investigational device exemption application to begin …
WISE has raised €30m ($34.8m) to advance the development of its spinal cord stimulation (SCS) device for chronic pain treatment. The …
The UK’s Labour government has ambitious plans to transform the country’s National Health Service (NHS) into one that is more …
Australian-based Memphasys and Monash IVF Group have finalised a 12-month exclusive national supply agreement for the Felix automated sperm selection …
New data from LivaNova has demonstrated the clinical benefit of its programming algorithm in patients with obstructive sleep apnoea (OSA). Trial …
Swiss medical device company Distalmotion has secured the US Food and Drug Administration (FDA) 510(k) clearance for its DEXTER robotic …
Penumbra has secured FDA approval for its Thunderbolt system, the first device to offer computer-assisted vacuum therapy (CAVT) for stroke …