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In the context of disability-related leave, an employer may top off a short-term disability benefit by paying the difference between the disability wage replacement (typically 60% of salary) and the employees full salary

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My question for you is, based on all the available data generated in the HELIOS-B study, combined with the Nucresiran trial data currently being generated, is it possible that the FDA could allow for an accelerated submission/approval for the ATTR-CM indication

It's one of the more credible "natural GLP-1" ingredients on the market for this reason

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