Lantheus wins FDA approval for Tauklarify tau PET imaging in Alzheimer’s evaluation
FDA approves Lantheus’ Tauklarify for Alzheimer’s tau PET imaging. See what the scan detects, where errors arise and what could limit access.
FDA approves Lantheus’ Tauklarify for Alzheimer’s tau PET imaging. See what the scan detects, where errors arise and what could limit access.
Nanochon gains Panama authorization for a five-patient Chondrograft study as its cartilage implant moves deeper into first-in-human testing.
FDA approves TAUKLARIFY for tau PET imaging in Alzheimer’s evaluation. See how Lantheus’ new tracer fits into the evolving diagnostic market.
Adaptyx and Attune begin a $4 million ARPA-H-backed study testing continuous biomarkers and focused ultrasound in 100 adults with chronic pain.
VB Spine has closed its CT-Fluoro deal with Augmedics. See why the xvision addition could widen access to AR spine navigation.
Galderma’s Restylane Shaype gains EU MDR approval for chin augmentation, bringing its high-firmness NASHA HD filler into Europe.
Labcorp Holdings Inc. (NYSE: LH) announced on August 10, 2026 that the U.S. Food and Drug Administration has approved PGDx elio tissue complete CDx as a companion diagnostic for identifying melanoma patients whose tumors carry BRAF V600E or BRAF V600K mutations and who may benefit from FDA-approved BRAF inhibitors or approved BRAF and MEK inhibitor
MindMaze Therapeutics finishes its neurology refocus while CHF 4 million of Neuro.io funding shifts to September and November. See what comes next.
Renew Biotechnologies has published peer-reviewed proof-of-concept research showing that native cell-free DNA methylation sequencing can recover neuron-associated blood signals that differ across Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. The results strengthen the scientific rationale behind its NeuroLens platform, but the decisive next step is independent, prospective validation in larger and more diverse patient
Nipro Corporation has commercially launched its FDA-cleared ELISIO-HX dialyzer in the United States, offering dialysis providers a medium cut-off membrane designed to remove larger uremic toxins through existing hemodialysis equipment and workflows.