Clinical Trials Directory

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RecruitingNCT06620809

The Safety and Efficacy of NouvSoma001 in Neuromyelitis Optica Spectrum Disorders

An Open-Label Exploratory Clinical Trial to Assess the Safety and Efficacy of NouvSoma001 in the Treatment of Neuromyelitis Optica Spectrum Disorders

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
69 (estimated)
Sponsor
Tongji Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is a single-center, randomized, open-label, placebo-controlled, dose-escalation trial. The objective of this research is to evaluate the safety, tolerability, and efficacy of intrathecal administration of human-induced neural stem cell-derived extracellular vesicles (NouvSoma001) for the treatment of neuromyelitis optica spectrum disorders.

Detailed description

This is a single-center, randomized, open-label, placebo-controlled, dose-escalation trial. The study consists of two parts: Part 1 is a dose-escalation study, while Part 2 is a dose-extension study based on the results of Part 1. Part 1 will follow a traditional 3+3 dose-escalation design, enrolling a total of 9 subjects. In Cohort 1, participants will receive 5 × 10\^9 particles; in Cohort 2, they will receive 1.5 × 10\^10 particles; and in Cohort 3, they will receive 3 × 10\^10 particles. If no dose-limiting toxicities (DLTs) are observed within 2 weeks after the initial administration, a new cohort will be enrolled at the next higher dose level. If DLTs are observed in 1 participant, another 2 participants will be treated at the same dose level. Dose escalation will cease if DLTs are observed in more than 33% of the participants. In Part 2, the remaining 60 participants will be randomized in a 2:1 ratio to the treatment and placebo groups, with the dose level determined by the Data Safety Monitoring Board based on the results of Part 1.

Conditions

Interventions

TypeNameDescription
DRUGExtracellular vesicles derived from human-induced neural stem cells for intrathecal injectionExtracellular vesicles derived from human-induced neural stem cells for intrathecal injection(5×10\^9 particles)
DRUGA placebo of extracellular vesicles derived from human-induced neural stem cells for intrathecal injectionExtracellular vesicles placebo(5×10\^9 particles)

Timeline

Start date
2025-03-28
Primary completion
2026-11-30
Completion
2027-11-30
First posted
2024-10-01
Last updated
2026-01-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06620809. Inclusion in this directory is not an endorsement.