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If regulatory submissions proceed as expected, the earliest plausible timeline for a market authorisation decision in the UK or Europe would be 2026 or 2027 though this is subject to the pace of regulatory review, the completeness of the submission package, and any additional data requests from the MHRA or EMA

For patients without coverage, compounded semaglutide and tirzepatide through telehealth represent the most practical cash-pay option

However, IV therapy may not be appropriate for everyone

EudraVigilance pharmacovigilance data When we look beyond controlled trials to real-world reporting, the picture gains complexity