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
| Type | Name | Description |
|---|---|---|
| DRUG | LIBERTAL- 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.