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An Open Label, Dose Escalation Study With A Double Blind Randomised Placebo Controlled Withdrawal To Examine The Effects Of The Histamine H3 Antagonist GSK189254 In Patients With Narcolepsy.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 18, 2026
NCT ID
NCT00366080
Status
TERMINATED
Phase
Phase 2
Sponsor
GlaxoSmithKline
Executive brief
Investment-Ready Snapshot
GSK189254, a histamine H3 receptor antagonist, was developed by GlaxoSmithKline for the treatment of narcolepsy. The study was terminated based on interim results indicating futility, suggesting that GSK189254 may not provide a significant therapeutic benefit over existing treatments. The narcolepsy market is competitive, with established therapies such as modafinil and sodium oxybate dominating. The termination of this trial may impact GSK's position in the narcolepsy treatment landscape, necessitating a reassessment of their pipeline and strategic focus in sleep disorder therapeutics. Investors and stakeholders should consider the implications of this outcome on GSK's R&D strategy and potential market share.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00366080
Indication
Narcolepsy
Modality
small molecule
Target
Histamine H3 receptor antagonist
Intervention
GSK189254
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.