CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 147 enrolled
Drug / intervention
RNS60drug
Likely dose
Not stated in 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/NCT03456882
NCT03456882Phase 2Completed

The Effect of RNS60 on ALS Biomarkers

Mario Negri Institute for Pharmacological Research·interventional·Posted Mar 7, 2018·Updated Apr 21, 2023

In Brief

A Phase 2 clinical trial evaluating RNS60 for Amyotrophic Lateral Sclerosis. Completed, enrolled 147 participants across 23 sites in 2 countries.

Detailed Summary

Amyotrophic Lateral Sclerosis (ALS) is a rare lethal neurodegenerative disease involving inflammation. Riluzole, the only drug for ALS, improves median survival by 3 months. This prompts new treatments of ALS. RNS60 is an experimental drug with favorable effects in preclinical studies of neuroinflammation and neurodegeneration. Based on significant efficacy demonstrated in preclinical studies and its excellent clinical safety profile, RNS60 is a promising candidate for a drug to treat ALS. Developing a pharmacodynamic marker will be a first and important step for dose finding and exploration of the mechanism of action in human, and pave the way to trials measuring drug efficacy. The Investigator propose a multicenter, randomized, double-blind, placebo-controlled, parallel group, Phase II trial. The study centers will be located in Italy and at Massachusetts General Hospital (MGH) in Boston. A total of 142 ALS patients will be randomly assigned to RNS60 or placebo (administered by intravenous infusion once/week and inhaled via nebulization every morning for 24 weeks). All participants will also take riluzole (50-mg tablet twice/day). Blood samples for biomarker analysis (protein, RNA) will be collected in the screening period, on day 1, week 4,12 and 24. Both safety and potential therapeutic effects of RNS60 will be also assessed.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesItaly, United States

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedMar 7, 2018
Enrollment StartMay 30, 2017
Primary CompletionNov 23, 2020
Study CompletionMay 30, 2021
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 8.3 years ago

Interventions

RNS60drug

normal saline plus oxigen in nanobubble