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NCT00366080TERMINATEDanonymous

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.

Sponsor

Source record

GlaxoSmithKline

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Histamine H3 receptor antagonist

Indication / condition

AI-normalized

Narcolepsy

Intervention

Source record

GSK189254

Source & freshness

Source record

NCT ID

NCT00366080

Original source

ClinicalTrials.gov

Source last updated

Mar 10, 2017

Ingested at

Jun 18, 2026

Internal sync

Jun 18, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT00366080

Title

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.

Sponsor

GlaxoSmithKline

Status

TERMINATED

Phase

Phase 2

Condition raw

Narcolepsy

Condition normalized

Narcolepsy

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Histamine H3 receptor antagonist

Target normalized

Histamine H3 receptor antagonist

Interventions

GSK189254

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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