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Initiation of a Phase 2 trial broadens the pipeline visibility and could trigger modest near-term upside on optimism for future data, though no results are disclosed and success is uncertain.
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Invivyd and the SPEAR Study Group announced the launch of FLINTLOCK, a Phase 2 trial evaluating high-dose VYD2311 for Long COVID and Post-Vaccination Syndrome. The study will measure safety, tolerability, pharmacokinetics, and clinical efficacy, signaling a push to broaden IVVD's monoclonal antibody portfolio beyond acute infections. The key near-term catalyst is safety and PK signals, with data readouts expected later if progress continues.
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