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Clinical Trials associated with LY-N001(Lingyi (Hangzhou) Biotechnology) / Not yet recruitingEarly Phase 1 A Prospective, Single-Arm, Single-Dose Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of Intracerebral Administration of LY-N001 Injection in Subjects With Moderate to Advanced Parkinson's Disease Carrying GBA1 Mutations
This is a prospective, single-arm, single-dose clinical study designed to evaluate the safety, tolerability, efficacy, immunogenicity, pharmacodynamic (PD) and pharmacokinetic (PK) profiles of LY-N001 Injection in patients with moderate-to-advanced Parkinson's disease carrying GBA1 mutations. The study consists of a main study phase and a long-term follow-up phase.
100 Clinical Results associated with LY-N001(Lingyi (Hangzhou) Biotechnology)
100 Translational Medicine associated with LY-N001(Lingyi (Hangzhou) Biotechnology)
100 Patents (Medical) associated with LY-N001(Lingyi (Hangzhou) Biotechnology)
100 Deals associated with LY-N001(Lingyi (Hangzhou) Biotechnology)