UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005637
Receipt number R000006639
Scientific Title An Open Label Study Comparing the Clinical Equivalence of Generic Pioglitazone Hydrochloride 15mg tablets (SAWAI) and ACTOS 15mg tablets
Date of disclosure of the study information 2011/05/24
Last modified on 2012/03/21 14:12:18

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Basic information

Public title

An Open Label Study Comparing the Clinical Equivalence of Generic Pioglitazone Hydrochloride 15mg tablets (SAWAI) and ACTOS 15mg tablets

Acronym

Clinical Equivalence of Generic Pioglitazone Hydrochloride 15mg tablets (SAWAI) and ACTOS 15mg tablets

Scientific Title

An Open Label Study Comparing the Clinical Equivalence of Generic Pioglitazone Hydrochloride 15mg tablets (SAWAI) and ACTOS 15mg tablets

Scientific Title:Acronym

Clinical Equivalence of Generic Pioglitazone Hydrochloride 15mg tablets (SAWAI) and ACTOS 15mg tablets

Region

Japan


Condition

Condition

Type 2 diabetic mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To prove the clinical equivalence between Generic Pioglitazone Hydrochloride 15mg (SAWAI) tablets and ACTOS Tablets 15 in type 2 diabetic patients

Basic objectives2

Bio-equivalence

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Change From Baseline in HbA1c at Week 12

Key secondary outcomes

Change From Baseline in Fasting Plasma Glucose at Week 12


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine Maneuver

Interventions/Control_1

Continue the same oral anti-diabetic drug and the diet/exercise regimen as the preceding 20 weeks for 4 weeks. At week 0, subjects were assigned to either Generic Pioglitazone Hydrochloride 15mg (SAWAI) tablets or ACTOS Tablets 15. Except for Pioglitazone Hydrochloride, the same treatments continue for another 12 weeks.

Interventions/Control_2

Continue the same oral anti-diabetic drug and the diet/exercise regimen as the preceding 20 weeks for 4 weeks. At week 0, subjects were assigned to either Generic Pioglitazone Hydrochloride 15mg (SAWAI) tablets or ACTOS Tablets 15. Except for Pioglitazone Hydrochloride, the same treatments continue for another 12 weeks.

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Type 2 diabetic outpatients over 20 years of age.
Treated with 15 mg daily of ACTOS tablets 15 over 20 weeks prior to week -4.
Treated with single or double or triple oral hypoglycemic agent including ACTOS tablets 15 over 20 weeks prior to week -4.
HbA1c <=7.0% from the data week -4.
Written informed consent.

Key exclusion criteria

History and/or complication of cardiac failure.
Need of insulin therapy.
Treated using three or more oral anti-diabetes drugs other than ACTOS tablets 15.
Renal or liver dysfunction.
Complication with or recent history of myocardial infarction, angina pectoris, cerebral stroke, and cerebral infarction.
Malignant neoplasms.
Severe ketosis, diabetic coma.
History of hypersensitive reaction to pioglitazone.
History of major gastrointestinal surgery.
Pregnancy.
History of alcohol abuse.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yasushi Fukushima

Organization

Tokyo-Eki Center-building Clinic

Division name

Department of Internal Medicine

Zip code


Address

3-14, Nihonbashi 3-chome, Chuo-ku, Tokyo, 103-0027 JAPAN

TEL

03-3517-6688

Email



Public contact

Name of contact person

1st name
Middle name
Last name Yasushi Fukushima

Organization

Tokyo-Eki Center-building Clinic

Division name

Department of Internal Medicine

Zip code


Address

3-14, Nihonbashi 3-chome, Chuo-ku, Tokyo, 103-0027 JAPAN

TEL

03-3517-6688

Homepage URL


Email



Sponsor or person

Institute

Tokyo-Eki Center-building Clinic

Institute

Department

Personal name



Funding Source

Organization

Tokyo-Eki Center-building Clinic

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

医療法人社団旭和会 東京駅センタービルクリニック(東京都)
財団法人柏市医療公社 柏市立柏病院(千葉県)
医療法人社団 阿佐谷クリニック(東京都)
芝パレスクリニック(東京都)
本田英比古クリニック(東京都)


Other administrative information

Date of disclosure of the study information

2011 Year 05 Month 24 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2010 Year 08 Month 30 Day

Date of IRB


Anticipated trial start date

2010 Year 10 Month 01 Day

Last follow-up date

2011 Year 07 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2011 Year 05 Month 24 Day

Last modified on

2012 Year 03 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006639


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name