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CompletedNCT02709187

DP-R208 Pharmacokinetic Study

DP-R208 Pharmacokinetic Study Phase I

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Alvogen Korea · Industry
Sex
Male
Age
19 Years – 55 Years
Healthy volunteers
Accepted

Summary

An open label, randomized, 2-sequence, 2-period, single-dose cross-over study to evaluate the pharmacokinetics characteristics of DP-R208 (Candesartan cilexetil 8mg/Rosuvastatin 10mg), a fixed dose combination compared with coadministration of separate constituents in healthy adult volunteers

Conditions

Interventions

TypeNameDescription
DRUGDP-R208Investigational product is prescribed to all of randomized subjects
DRUGCandesartan cilexetilInvestigational product is prescribed to all of randomized subjects
DRUGRosuvastatinInvestigational product is prescribed to all of randomized subjects

Timeline

Start date
2016-03-01
Primary completion
2016-05-01
Completion
2016-05-01
First posted
2016-03-15
Last updated
2016-06-08

Source: ClinicalTrials.gov record NCT02709187. Inclusion in this directory is not an endorsement.

DP-R208 Pharmacokinetic Study (NCT02709187) · Clinical Trials Directory