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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00344370
Other study ID # NK-104-310
Secondary ID
Status Completed
Phase Phase 3
First received June 23, 2006
Last updated January 25, 2010
Start date August 2006
Est. completion date April 2008

Study information

Verified date January 2010
Source Kowa Research Europe
Contact n/a
Is FDA regulated No
Health authority Poland: Ministry of HealthGermany: Ethics CommissionIndia: Indian Council of Medical Research
Study type Interventional

Clinical Trial Summary

This is a sixteen-week double-blind active-controlled follow-on and 28-week single-blind extension study for patients who participated in study NK-104-305.


Recruitment information / eligibility

Status Completed
Enrollment 214
Est. completion date April 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Type II diabetes mellitus

- Combined dyslipidemia

- Completed NK-104-305 (NCT00309751)

Exclusion Criteria:

- Withdrawal from NK-104-305 (NCT00309751)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Drug:
Pitavastatin
Pitavastatin 4 mg QD
Atorvastatin
Atorvastatin 40 mg

Locations

Country Name City State
Denmark CCBR Aalborg Aalborg
Denmark CCBR A/S Vejle
Denmark CCBR Vejle Vejle
Germany Gemeinschaftspraxis am Bahnhof Berlin-Spandau
Germany Pharmakologisches Studienzentum Chemnitz Chemnitz
Germany Internistische Diabetische Schwerpunktpraxis Dr. Frankfurt Am Main
Germany Internistische Gemeinschaftspraxis Mainz
Germany Gemeinschaftspraxis Dr. Senftleber, Dr. Kohler Messkirch
India Bhagwan Mahaveer Jain Heart Centre Bangalore
India Sri Ramachandra Medical College Hospital Chennai
India Apollo Hospitals Hyderabaad
India CARE Group of Hospitals Hyderabaad
India PD Hinduja Hospital Mumbai
Netherlands Andromed Breda Breda
Netherlands Andromed Eindhoven Eindhoven
Netherlands Andromed Noord Groningen
Netherlands Andromed Leiden Leiden
Netherlands Andromed Nijmegen Nijmegen
Netherlands Andromed Rotterdam Rotterdam
Netherlands Andromed Oost Velp
Netherlands Andromed Zoetermeer Zoetermeer
Poland Podlaski Osrodek Kardiologii Bialystok
Poland NZOZ GCP Dobra Praktyka Lekaska Gruziadz
Poland NZOZ Terapia Optima Katowice
Poland NZOZ Esculap, Przychodnia Lekary Rodzinnych Losice
Poland NZOZ Centrum, Poradnia Kardiologiczna Siedlce
Poland Spec. Gab. Lek. Internistyczno-Kardiologicznly Tarnow
Poland Woj.Szp.Spec.Nr 1 im. Prof. J. Gasinskiego Tychy
Poland Instytut Zywnosci i Zywienia Warszawa
Poland Lecznica PROSEN SMO Warszawa
Poland Szpital Wolski,im. Dr A. Gostynskiej Warszawa
United Kingdom Synexus Reading Clinical Research Centre Berkshire
United Kingdom Synexus Lancashire Clinical Research Centre Lancashire
United Kingdom Synexus Merseyside Clinical Research Centre Liverpool
United Kingdom Synexus Manchester Clinical Research Centre Manchester

Sponsors (1)

Lead Sponsor Collaborator
Kowa Research Europe

Countries where clinical trial is conducted

Denmark,  Germany,  India,  Netherlands,  Poland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary NCEP LDL-C Target Attainment 44 weeks No
Secondary Percent Change From Baseline in LDL-C Basseline to 44 weeks No
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