Based on the typical UK regulatory pathway, the most realistic timeline is: Late 2026 / early 2027: Eli Lilly expected to submit regulatory filings to the FDA and MHRA following completion of the remaining TRIUMPH Phase 3 readouts Late 2027 to mid-2028: Possible MHRA marketing authorisation, allowing private UK prescribing 2028 to 2029 onwards: Possible NHS availability following a NICE technology appraisal and NHS commissioning decisions Timelines may differ across the four UK nations, as Scotland, Wales, and Northern Ireland assess medicines separately through the Scottish Medicines Consortium (SMC), All Wales Medicines Strategy Group (AWMSG), and the Department of Health Northern Ireland respectively
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Both formulations are administered subcutaneously in the abdomen, thigh, or upper arm on the same day each week, with or without meals
Fishy body odor: High doses can lead to trimethylamine buildup, producing a distinctive odor in some patients
[DOI] [PMC free article] [PubMed] [Google Scholar] 80.Muraleedharan R, Dasgupta B
This was a much larger multi-centre study over a longer period of time (5 years)