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Ventyx Biosciences Announces Initiation of Dosing in a Phase 2a Trial of VTX3232 in Patients with Early Parkinson’s Disease
Ventyx Biosciences (Nasdaq: VTYX) has initiated dosing in a Phase 2a trial of VTX3232 for early Parkinson's disease. The trial aims to evaluate the drug's effects on disease- and target-relevant biomarkers, including exploratory PET neuroimaging to measure its impact on microglial activation. This study is based on evidence suggesting a strong mechanistic rationale for targeting NLRP3-driven neuroinflammation in Parkinson's disease.
The trial will enroll about ten patients for a 28-day open-label treatment period. Its primary endpoint is safety and tolerability, with additional measures including pharmacokinetics and relevant biomarkers in plasma and cerebrospinal fluid. Topline results are expected in 2025.
The trial will enroll about ten patients for a 28-day open-label treatment period. Its primary endpoint is safety and tolerability, with additional measures including pharmacokinetics and relevant biomarkers in plasma and cerebrospinal fluid. Topline results are expected in 2025.
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