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However, because of the time required to assess long-term clinical endpoints, both regulatory agencies have advised earlier evaluation of intermediate/surrogate histological endpoints to accelerate regulatory approval, given the unmet medical need for MASH pharmacotherapies [6]

The decision to move to 12mg depends on weight loss progress, side effect experience, and individual goals

The safest approach

Nothing in this article constitutes a claim that any compounded product is clinically proven, has been evaluated in clinical trials, or produces the same results as any FDA-approved drug

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