A Phase 1 Clinical Trial to Investigate Pharmacokinetics and Drug Interaction of Crestor and Glucodown OR SR in Healthy Volunteers

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Yuhan Corporation
ClinicalTrials.gov Identifier:
NCT01526317
First received: February 1, 2012
Last updated: July 31, 2012
Last verified: July 2012

February 1, 2012
July 31, 2012
December 2011
May 2012   (final data collection date for primary outcome measure)
  • AUCtau [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
  • Css,max [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01526317 on ClinicalTrials.gov Archive Site
  • AUCss,last [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
  • AUCss,inf [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
  • Css,min [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
  • Tss,max [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
  • t1/2 [ Time Frame: 72 hr ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
A Phase 1 Clinical Trial to Investigate Pharmacokinetics and Drug Interaction of Crestor and Glucodown OR SR in Healthy Volunteers
A Randomized, Open Label, Cross-over Clinical Trial to Investigate Pharmacokinetics and Drug Interaction of Crestor and Glucodown OR SR in Healthy Volunteers

This clinical trial is designed to compare the pharmacokinetic characteristics of combination and separate administration of Crestor(Rosuvastatin) and Glucodown(Metformin SR). Also investigate drug interaction between separate and combination administration.

Total number of subjects is 36. 6 group(6 for 1 group), 3 period, consecutive 5 day administration, 10 days washout after 5th day of administration.

All subjects take Crestor alone, Glucodown alone, Crestor+Glucodown combination during 3 each period.

Not Provided
Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Crossover Assignment
Masking: Open Label
Pharmacokinetics and Drug Interaction of Crestor and Glucodown SR
Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
For co-administration,Crestor 1 tablet and Glucodown 1 tablet a day for 5 day.(1 period) For separate administration, Crestor 1 tablet a day for 5 day and Glucodown 1 tablet a day for 5 day.
  • Experimental: 1
    This arm is consist of 6 subject. Crestor 10mg and Glucodown 750mg for 5 day during period 1. Crestor 10mg alone for 5 day during period 2. Glucodown 750mg alone for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
  • Experimental: 2
    This arm is consist of 6 subject. Glucodown 750mg alone for 5 day during period 1. Crestor 10mg and Glucodown 750mg for 5 day during period 2. Crestor 10mg alone for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
  • Experimental: 3
    This arm is consist of 6 subject. Crestor 10mg alone for 5 day during period 1. Glucodown 750mg alone for 5 day during period 2. Crestor 10mg and Glucodown 750mg for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
  • Experimental: 4
    This arm is consist of 6 subject. Glucodown 750mg alone for 5 day during period 1. Crestor 10mg alone for 5 day during period 2. Crestor 10mg and Glucodown 750mg for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
  • Experimental: 5
    This arm is consist of 6 subject. Crestor 10mg alone for 5 day during period 1. Crestor 10mg and Glucodown 750mg for 5 day during period 2. Glucodown 750mg alone for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
  • Experimental: 6
    This arm is consist of 6 subject. Crestor 10mg and Glucodown 750mg for 5 day during period 1. Glucodown 750mg alone for 5 day during period 2. Crestor 10mg alone for 5 day during period 3.
    Intervention: Drug: Crestor 10mg(Rosuvastatin 10mg), Glucodown OR SR 750mg(Metformin SR 750mg)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
36
May 2012
May 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 20~50 yrs old, healthy Korean Subjects
  • Body weight <ideal body weight±20%
  • No congenital, chronic disease, No current disease
  • Subjects who are diagnosed to include by medical doctor from laboratory and ECG result.
  • Subjects who agree to keep contraceptive methods during the clinical trial.

Exclusion Criteria:

  • Subjects who are allergic to investigational drug.
  • Subjects who have a medical history which can affect the clinical trial.
  • Hypertension(Systolic BP ≥ 150mmHG or Diastolic BP ≥ 100mmHg), Hypotension(Systolic BP ≤ 100mmHg or Diastolic BP ≤ 65mmHg)
  • Subjects who have taken other medicine in recent 2~4 weeks.
  • Subjects who have a risk of hypoglycemia and imbalance in taking a diet.
Both
20 Years to 50 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
NCT01526317
YH14755-101
No
Yuhan Corporation
Yuhan Corporation
Not Provided
Principal Investigator: Kyungsu Park, MD, Ph.D Severance Hospital, Yonsei University
Yuhan Corporation
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP