drugset / Trial / NCT03401541

25-Hydroxyvitamin D Pharmacokinetic Study

NCT03401541

Phase 0 Completed 16 enrolled Boston University
RandomizedCrossoverDouble-blindTreatment

Summary

To evaluate the pharmacokinetic parameters of orally administered 25-hydroxyvitamin D3 \[25(OH)D3\] and vitamin D3 from the corresponding serum concentration-time curves in healthy adults and adults with a history of intestinal malabsorption.

Timeline

Start
2018-10-01
Primary completion
2019-04-01
Completion
2019-11-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcifediol Unknown 900 ug Oral
Subject Vitamin D Other / unclassified 900 ug Oral