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Active Not RecruitingNCT07027111

Safety, Tolerability, and Efficacy of NVG-2089 in Participants With CIDP

A Phase 2, Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of Intravenous NVG-2089 in Participants With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Nuvig Therapeutics, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the safety of NVG-2089 and to evaluate how well patients respond to this investigational treatment. NVG-2089 is a new drug that is being developed for treating patients with CIDP. NVG-2089 is designed to mimic the effects of a protein called IVIg. NVG-2089 is designed to potentially help the immune system by attaching (binding) to certain receptors in the body and activating them, which helps reduce inflammation and supports how the immune system works.

Conditions

Interventions

TypeNameDescription
DRUGNVG-2089Study drug

Timeline

Start date
2025-04-25
Primary completion
2026-07-31
Completion
2026-07-31
First posted
2025-06-18
Last updated
2026-04-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07027111. Inclusion in this directory is not an endorsement.

Safety, Tolerability, and Efficacy of NVG-2089 in Participants With CIDP (NCT07027111) · Clinical Trials Directory