TrialSignal
Clinical trial intelligence report
A Study to Evaluate the Efficacy and Tolerability of Clobetasol Propionate vs. Vehicle in the Treatment of Mild to Moderate Plaque-Type Psoriasis
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT00842153-Jun 24, 2026
NCT ID
NCT00842153
Status
COMPLETED
Phase
Phase 4
Sponsor
Stiefel, a GSK Company
Executive brief
Investment-Ready Snapshot
Clobetasol propionate foam, marketed as Olux-E, is positioned to address the significant market for topical treatments in mild to moderate plaque-type psoriasis, which affects millions globally. The competitive landscape includes other topical corticosteroids and biologics. The completion of this trial reinforces the product's efficacy and safety profile, potentially enhancing its market share against competitors. Diligence should focus on post-marketing surveillance and any emerging data on long-term safety and efficacy.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00842153
Indication
Psoriasis
Modality
small molecule
Target
Clobetasol propionate acts as a potent anti-inflammatory agent by binding to the glucocorticoid receptor, leading to the modulation of gene expression involved in inflammatory and immune responses.
Intervention
Clobetasol propionate foam, Vehicle foam
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.