Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
37 participants
INTERVENTIONAL
2016-03-31
2016-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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RT group
combination dose of Candesartan and Rosuvastatin and DP-R208 in order
DP-R208
Investigational product is prescribed to all of randomized subjects
Candesartan cilexetil
Investigational product is prescribed to all of randomized subjects
Rosuvastatin
Investigational product is prescribed to all of randomized subjects
TR group
DP-R208 and combination dose of Candesartan and Rosuvastatin in order
DP-R208
Investigational product is prescribed to all of randomized subjects
Candesartan cilexetil
Investigational product is prescribed to all of randomized subjects
Rosuvastatin
Investigational product is prescribed to all of randomized subjects
Interventions
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DP-R208
Investigational product is prescribed to all of randomized subjects
Candesartan cilexetil
Investigational product is prescribed to all of randomized subjects
Rosuvastatin
Investigational product is prescribed to all of randomized subjects
Eligibility Criteria
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Inclusion Criteria
* signed the informed consent form prior to the study participation
Exclusion Criteria
* Previously donate whole blood within 60 days or component blood within 14 days
* Clinically significant allergic disease
* Taken IP in other trial within 90 days
* An impossible one who participates in clinical trial by investigator's decision including laboratory test result
19 Years
55 Years
MALE
Yes
Sponsors
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Alvogen Korea
INDUSTRY
Responsible Party
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Other Identifiers
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DP-CTR208-I-04
Identifier Type: -
Identifier Source: org_study_id
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