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Assessing PACS is challenging, and reviewing current therapeutic options while proposing a triad of potential therapeutic elements will add value to clinical assays and guidelines

Under standard review timelines, that places potential FDA approval somewhere around mid to late next year

It can be an opportunity to pick up new presentations, or help people to understand the extent of their behaviour, she says

While there is no definitive evidence that slightly early dosing increases pancreatitis risk, maintaining appropriate intervals between doses is a prudent safety measure

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