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Anyone involved in the legitimate preparation of retatrutide within a clinical trial setting should follow the sponsor's protocol and their institution's aseptic preparation and beyond-use dating policies, as outlined by the SPS and relevant regulatory guidance

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Pharmacokinetic analyses confirmed therapeutic intraparenchymal temozolomide concentrations for over four weeks coupled with negligible systemic exposure

Additional criteria may be used to make a final award, e.g., potential professional impact of the awardee, other concurrent CUGH awards, and diversity vis a vis other awardees