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Propylene glycol, skin sensitisation and allergic contact dermatitis: a scientific and regulatory conundrum
The needle is thin and the injection is quick (under 1 minute)
The changes in 20242025 reflect that philosophy: ensuring MA enrollees get what theyre entitled to (no more, but also no less), and that plans compete on value rather than on cherry-picking or marketing tricks
The retatrutide availability timeline depends on ongoing clinical trials and regulatory review: Current status: Multiple phase 3 trials (TRIUMPH program) ongoing Phase 3 primary completion: Expected through mid-year NDA submission: Eli Lilly expected to submit to FDA in late future FDA review period: Approximately 10 months after submission Estimated approval: Potentially late next year at earliest Commercial launch: Could follow shortly after approval It is important to note that Eli Lilly has not announced an official filing timeline
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