CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 536 enrolled
Drug / intervention
Arbaclofen +1 moredrug
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/NCT03290131
NCT03290131Phase 3Completed

A Randomized, Double-Blind, Placebo-Controlled Parallel Group Study to Investigate the Safety and Efficacy of Arbaclofen Extended-Release Tablets for the Treatment of Spasticity in Patients With Multiple Sclerosis

RVL Pharmaceuticals, Inc.·interventional·Posted Sep 21, 2017·Updated Jul 15, 2022

In Brief

A Phase 3 clinical trial evaluating Arbaclofen and Placebo for Multiple Sclerosis and Spasticity, Muscle. Completed, enrolled 536 participants across 30 sites in 7 countries.

Detailed Summary

Multiple Sclerosis (MS) is an acquired inflammatory demyelinating disease of the central nervous system (CNS) that is regarded as the foremost cause of non-traumatic neurologic disability in adults in North America. Spasticity is a common complication in MS and occurs in up to 84% of patients. The main sign of spasticity is resistance to passive limb movement characterized by increased resistance to stretching, clonus, and exaggerated deep reflexes. Osmotica Pharmaceutical is currently developing arbaclofen extended-release tablets (AERT) for the treatment of spasticity in patients with MS.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelarus, Bosnia and Herzegovina, Bulgaria, Croatia, Moldova, Poland, Serbia

Timeline

Phase 3CompletedFinished
201820192020202120222023202420252026
First PostedSep 21, 2017
Enrollment StartJan 28, 2018
Primary CompletionDec 3, 2018
Study CompletionJan 2, 2019
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 8.8 years ago

Interventions

Arbaclofendrug

Arbaclofen Extended Release Tablet

Placebodrug

Placebo comparator