CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 30 enrolled
Drug / intervention
Intranasal auto-M2-BFsdrug
Likely dose
Intranasal auto-M2-BFs 2.0 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02957123
NCT02957123Phase 2Completed

Safety/Efficacy of Intranasally-Administered Bioactive Factors Produced by Autologous M2 Macrophages in Patients With Organic Brain Syndrome

Russian Academy of Medical Sciences·interventional·Posted Nov 7, 2016·Updated Feb 18, 2021

In Brief

A Phase 2 clinical trial evaluating Intranasal auto-M2-BFs for Organic Brain Syndrome, Nonpsychotic and 8 related conditions. Completed, enrolled 30 participants across 1 site.

Detailed Summary

The investigators have designed an innovative proof-of-concept trial designed to provide data as to whether the treatment/rehabilitation efficacy and functional outcome of patients with organic brain syndrome are improved with intranasal inhalations of bioactive factors (BF), produced by autologous M2 macrophages (auto-M2-BFs). The rationale for this approach is the ability of central nervous system to repair and the important role of macrophages in the regulation of this process. It was found that type 2 macrophages have anti-inflammatory and reparative potential, whereas M1 cells possess pro-inflammatory and neurotoxic effects. Action of M2 macrophages is largely realized through the production a wide variety of bioactive factors (cytokines, chemokines, growth factors, neuropeptides, microvesicles etc) that inhibit inflammation, protect neurons from apoptosis, stimulate neurogenesis, the growth and remyelination of axons, the formation of new synapses and activate angiogenesis. This study uses auto-M2-BFs, as therapeutic agents and intranasal administration focusing on nose to brain transport, as a mode of delivery. Expected clinical effects in treated subjects: improvement of cognitive functions (memory, language, attention); correction of focal neurological deficit (paresis, spasticity, sensory disorders); reduction vestibular/ataxic disorders (vertigo, unsteadiness when walking); reduction of headaches; reduction of asthenia (weakness, fatigue); correction of emotional disorders (anxiety, depression).

Study Details

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 7, 2016
Enrollment StartMar 1, 2016
Primary CompletionSep 1, 2020
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 9.7 years ago

Interventions

Intranasal auto-M2-BFsdrug

Delivery is performed with the aerosol inhaler device (nebulizer), 2.0 mL once a day up to 30 days.