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Estimation of Dose Proportionality of Darapladib - 107038 - Pharmacodynamics Post Dose Data - [Analyte and PD sample type]

- 12-11-18 - 1 Formulier, 12 Itemgroepen, 16 Data-elementen, 1 Taal

Itemgroepen: Administrative data, Predose, 0.5 hour post dose, 1 hour post dose, 2 hours post dose, 3 hours post dose, 4 hours post dose, 6 hours post dose, 9 hours post dose, 12 hours post dose, 18 hours post dose, 24 hours post dose

Study ID: 107038 Clinical Study ID: LPL107038 Study Title: Study to Estimate the Dose Proportionality of the Enteric-Coated Freebase Formulation of SB-480848 Patient Level Data: Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: Tyrisa ,US Study Indication: Atherosclerosis

Clinical Trial
Sampling Studies
Laboratories
Clinical Trial, Phase I
Atherosclerosis

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Estimation of Dose Proportionality of Darapladib - 107038 - Pharmacodynamics Post Dose Data - [Analyte and PD sample type]

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Estimation of Dose Proportionality of Darapladib - 107038 - Pharmacodynamics Post Dose Data - [Analyte and PD sample type]

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