Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Phase I/II Clinical Study to Evaluate the Safety and Efficacy of VGN-R08b in Patients With Type III Gaucher's Disease

A phase I/II clinical study to evaluate the tolerance, safety and efficacy of VGN-R08b intracerebroventricular injection in patients with type III Gaucher's disease

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: 2-18Biological sex: AllType: InterventionalSponsor: Shanghai Vitalgen BioPharma Co., Ltd.Updated: May 22, 2026
Eligibility criteria

The signing of the informed consent form should be completed when the subject is... [+8]

There are other serious neurological disorders that may cause symptoms of Gauche... [+8]

Status: Not yet recruiting

A Safety Study of Contralateral Eye Dosing of VGR-R01 in Participants With Bietti's Crystalline Dystrophy (BCD)

This is a multi-centre, single- arm, non-randomized, open-label phase 1/2 clinical trial which enables dosing of the fellow eyes of patients who received VGR-R01 administration in previous studies.

Participants needed: 15
Trial details
Phase: Phase 1, Phase 2Age: 18-69Biological sex: AllType: InterventionalSponsor: Shanghai Vitalgen BioPharma Co., Ltd.Updated: May 14, 2026Locations: 2
Eligibility criteria

Participants received VGR-R01 administration in the VGR-R01-001 or VGR-R01-101 s... [+2]

Have insufficient viable retinal photoreceptor cells based on investigator's dec... [+8]

Status: Recruiting

A Study to Evaluate the Tolerability, Safety and Efficacy of VGM-R02b

Phase I, open-label, single-arm, single-dose, trial of VGM-R02b (gene replacement therapy) in patients with Glutaric Acidemia Type I (GA-I) who meet enrollment criteria and are genetically confirmed by GCDH gene mutation. 1 to 3 patients aged≤ 6 years at the time of screening will be enrolled in each dose group in the dose escalation part. In the dose expansion part, the sample size will be statistically calculated and adjusted according to the efficacy and safety data in the dose escalation part.

Participants needed: 12
Trial details
Phase: Phase 1Age: Up to 6Biological sex: AllType: InterventionalSponsor: Shanghai Vitalgen BioPharma Co., Ltd.Updated: May 13, 2026Locations: 1
Eligibility criteria

Subjects must be ≤ 6 years; [+4]

Participation in gene therapy or stem cell transduction therapy at any time prio... [+17]

Status: Not yet recruiting

A Trial to Evaluate Safety and Efficacy of a Product Named VGN-R08b in Parkinson's Disease Patients With GBA1 Mutations

A Phase I/II Clinical Study to Evaluate the Tolerability, Safety, and Efficacy of VGN-R08b Intra-cerebroventricular injection in Parkinson's Disease Patients with GBA1 Mutations

Participants needed: 17
Trial details
Phase: Phase 1, Phase 2Age: 30-70Biological sex: AllType: InterventionalSponsor: Shanghai Vitalgen BioPharma Co., Ltd.Updated: May 1, 2026Locations: 1
Eligibility criteria

Male or female, aged 30 to 70 years (inclusive) at the time of signing the infor... [+10]

Subject has any of the following diseases or disease history [+11]