Trials / Completed
CompletedNCT01726933
LAS41008 in Moderate to Severe Chronic Plaque Psoriasis
A Multi-center, Randomized, Double-blind, Three-arm, 16 Week, Adaptive Phase III Clinical Study to Investigate the Efficacy and Safety of LAS41008 vs LASW1835 and vs Placebo in Patients With Moderate to Severe Chronic Plaque Psoriasis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 839 (actual)
- Sponsor
- Almirall, S.A. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to evaluate the efficacy and safety of LAS41008 in comparison to active control and placebo in patients with moderate to severe chronic plaque psoriasis
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LAS41008 | gastric resistant tablet, weekly up-titration up to maximal tolerated dosage |
| DRUG | LASW1835 | gastric resistant tablet, weekly up-titration up to maximal tolerated dosage |
| DRUG | Placebo | gastric resistant tablet, weekly up-titration up to maximal tolerated dosage |
Timeline
- Start date
- 2012-11-01
- Primary completion
- 2014-10-01
- Completion
- 2015-11-01
- First posted
- 2012-11-15
- Last updated
- 2015-12-02
Locations
4 sites across 4 countries: Austria, Germany, Netherlands, Poland
Source: ClinicalTrials.gov record NCT01726933. Inclusion in this directory is not an endorsement.