Bioavailability of Infacort When Administered Onto Food Compared to Direct Oral Administration
Status:
Completed
Trial end date:
2017-07-26
Target enrollment:
Participant gender:
Summary
This is a single centre, open-label, randomised, single dose, three-period, crossover study
to evaluate the bioavailability of Infacort® administered as 'sprinkles' with soft food and
yoghurt compared with direct administration to the back of the tongue in
dexamethasone-suppressed healthy adult male subjects.
The study will comprise of a pre-study screen, followed by 3 treatment periods and a
post-study follow-up.
Phase:
Phase 1
Details
Lead Sponsor:
Diurnal Limited
Collaborators:
Brush Clinical Research Ltd. EMAS Pharma Emas Pharma Ltd. Medical Matters International Ltd. Simbec Research Voet Consulting