Clinical Trials Directory

Trials / Completed

CompletedNCT00317213

Smoking Cessation Assistance With LIBERTAL, A Phospholipid Mixture

Phase IIB Study of the Efficacy and Safety of LIBERTAL, A Phosphatidic-Acid-Enriched Phospholipid, on Smoking Cessation

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
500 (planned)
Sponsor
Kaplan Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

It has been shown in rodent models that chronic substance abuse is associated with a rigidification of cell membrane fluidity due to a change in the membrane cholesterol/phospholipids ratio. Upon substance withdrawal the membrane undergoes reequilibration of this ratio, a process resulting both in an acute and a prolonged severe withdrawal syndrome. MBM has developed a patented,phosphatidic acid-enriched phospholipid platform ("LIBERTAL"), which is supposed to facilitate the membrane fluidity recovery. The company has focused on nicotine withdrawal in smoking cessation,as primary target.

Detailed description

A randomized,double-blind, dose-finding,phase IIB study with Libertal has been performed in 493 volunteer smokers, wishing to quit. They were divided into 5 arms: 4 treatment groups of 0.5, 1.0, 2.0 and 4.0g/day respectively, and one placebo, divided BID. Treatment was administered during one week prior to smoking cessation, then continued during 8 weeks (56 days), followed by another 4 weeks without treatment (up to day 84). The primary endpoint was complete smoking cessation during at least 28 consecutive days. There were 6 on-site visits and 4 telephone interviews.

Conditions

Interventions

TypeNameDescription
DRUGLIBERTAL- a phospholipid mixture

Timeline

Start date
2002-02-01
Completion
2002-07-01
First posted
2006-04-24
Last updated
2008-04-14

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00317213. Inclusion in this directory is not an endorsement.