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Clinical Trial Summary

Study to investigate if the uptake of Ticagrelor into the body differs depending on method of administration.


Clinical Trial Description

Study to evaluate the bioavailability of the crushed ticagrelor tablets when administered orally or through nasogastric tubes compared to whole ticagrelor tablets given orally ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms

  • Bioavailability Heathy Volunteers

NCT number NCT01887626
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 1
Start date July 2013
Completion date September 2013