We still need the "RC220 Toxicology and Safety Pharmacology" data. Then patent lodgements, ethics approval, trial site onboarding etc. Would not expect first patient before Q2 CY24.
Near term SP inflection points more likely to be Sheba 2.0 results or licensing agreement.
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- Ann: RC220 Peripheral Infusion Safety Confirmed
Ann: RC220 Peripheral Infusion Safety Confirmed, page-19
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