The First US Tinnitus Guideline Update Since 2014 Names Bimodal Neuromodulation, Handing Neuromod’s Lenire a Coverage Argument
A guideline listing is the first thing a payer asks a device maker for, and Neuromod’s Lenire now has one in tinnitus.
The daily shorts. One story, one insight.
A guideline listing is the first thing a payer asks a device maker for, and Neuromod’s Lenire now has one in tinnitus.
The gap over Skyrizi widened from week 12 to week 24, the stronger signal in an open-label study without placebo.
Germany is widening cancer screening where the evidence is settled and reopening it where cost is the question.
Roche is paying platform money for ADCs that do not exist yet, five times what it paid Hansoh for a clinical asset in 2025.
A hospital can meet every CMS posting rule and still face an FTC deception case over the estimate a patient receives.
The drug file reaches manufacturers, and the schema due around May 2027 decides how much net price becomes public.
Only one Member State was assessing each valve when Brussels chose them, so the joint report will frame the evidence.
Hanmi’s GLP-1 trails Wegovy and Mounjaro on weight loss, so its case rests on a low starting price and Korean supply.
Denmark turned a January no on Tecartus into a yes by tying price to response, and renewed burosumab on a lower price.
ICER has handed payers the case for putting Baxfendy behind generics, and Mineralys gets its price anchor before launch.