Clinical trials

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Condition / disease
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Status: Not yet recruiting

Phase I/II Clinical Study to Evaluate the Safety, Tolerability and Efficacy of LY-M003 Injection in Adult Patients With Wilson's Disease

This is a multicenter, open-label, single-arm, single-dose Phase I/II clinical study. It aims to evaluate the safety, tolerability, efficacy, immunogenicity, pharmacodynamic (PD) and pharmacokinetic (PK) profiles of LY-M003 Injection in patients with Wilson's Disease (WD).

Participants needed: 18
Trial details
Phase: Phase 1, Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Lingyi Biotech Co., Ltd.Updated: Jul 2, 2026Locations: 1
Eligibility criteria

The subject fully comprehends the purpose, design, methods and possible adverse... [+7]

AAV8 neutralizing antibody titer > 1:10 . [+24]

Status: Recruiting

A Clinical Study Evaluating LY-M001 Injection in the Treatment of Adult Patients With Type I Gaucher Disease

Gaucher disease (GD) is caused by mutations in the GBA1 gene, which leads to a lack or reduction of GCase activity. The consequences of this deficiency are generally attributed to the accumulation of the GCase substrate, Glucosylceramide (GlcCer), in macrophages in the liver, spleen, kidney, bone, lung, and even the brain, inducing their transformation into Gaucher cells whose cell cytoplasm presenting a characteristic "crumpled tissue paper" appearance, leading to pathological changes in involved tissues and organs.LY-M001 Injection is an rAAV8 vector gene therapy product. It can specifically transduce the target organ liver after a single intravenous administration and express the GCase protein in liver cells for a long period of time.

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Lingyi Biotech Co., Ltd.Updated: Jan 26, 2026Locations: 3
Eligibility criteria

Age ≥ 18 years and ≤ 60 years, male or female. [+10]

AAV8 neutralizing antibody positive (Antibody titer > 1:40). [+21]