UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000011666
Receipt number R000013639
Scientific Title Peginterferon or conventional interferon sequential entecavir treatment for hepatitis B e antigen positive chronic hepatitis B patients: a prospective randomized controlled trial
Date of disclosure of the study information 2013/09/09
Last modified on 2017/09/11 23:30:46

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Basic information

Public title

Peginterferon or conventional interferon sequential entecavir treatment for hepatitis B e antigen positive chronic hepatitis B patients: a prospective randomized controlled trial

Acronym

Peginterferon or conventional interferon sequential entecavir treatment

Scientific Title

Peginterferon or conventional interferon sequential entecavir treatment for hepatitis B e antigen positive chronic hepatitis B patients: a prospective randomized controlled trial

Scientific Title:Acronym

Peginterferon or conventional interferon sequential entecavir treatment

Region

Japan


Condition

Condition

chronic hepatitis B

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Efficacy and safety of peginterferon or conventional interferon sequential entecavir treatment for chronic hepatitis B patients

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

The reduction of HBsAg (<1,000 IU/mL) at 48 weeks after initiating entecavir treatment

Key secondary outcomes

1. The following outcomes at 48 weeks after entecavir treatment (a) HBeAg seroconversion rates (b) The reduction of HBV DNA levels (<5.0 logcopies/mL) (c) ALT normal rates (d) HBeAg seroclearance (e) HBsAg seroclearance (f) HBsAg seroconversion
2. Kinetics of HBV DNA levels
3. Kinetics of HBsAg levels
4. Kinetics of HB core-related antigen levels
5. The chenge of immunological markers
6. The regression of liver fibrosis (measured by Fibroscan)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

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

Interventions/Control_1

Pegiterferon induction arm

Interventions/Control_2

Conventional interferon (natural IFN-alpha) induction arm

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

# Chronic hepatitis B patients with HBeAg positivity
# Twice or more ALT flares
# HBV DNA levels > 4.0 log copies/mL

Key exclusion criteria

1. Prior exposure of interferon, antiviral agents, antitumoral agents, immunosupressive drugs, and radiotherapy within 6 months
2. HCV RNA positivity
3. Complicating other liver disease
4. The diagnosis of Liver cirrhosis, hepatic failure, and liver cancer
5. The history of hepatic encephalopathy, varices bleeding, and ascites
6. Complicating collagen disease
7. The history of interstitial pneumonia
8. Severe heart disease
9. The history of epilepsy
10. The history of depression
11. The history of abnormal thyroid function
12. The history of stroke
13. Severe diabetes
14. The history of malignant tumor within 5 years
15. The history of liver, kidney or bone marrow transplantation
16. Retinopathy
17. blood test abnormality as follows:
(a) neutrophil < 1,500 /mm3
(b) platelets count < 90,000/ mm3
(c) Hb < 10 g/dL
(d) prothrombin time > 20s or < 60%
(e) ALT > 10 times ULN
(f) total bilirubin > 2.0 mg/dL
(g) albmin < 3.2 g/dL
(h) creatinine clearance < 50 mL/min
18. Pregnancy
19. Doctors condider inadequate

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiromitsu Kumada

Organization

Toranomon Hospital

Division name

Hepatology

Zip code


Address

1-3-1 Kajigaya Takatsu-ku Kawasaki Kanagawa

TEL

044-877-5111

Email

kumahiro@toranomon.gr.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tetsuya Hosaka

Organization

Toranomon Hospital

Division name

Hepatology

Zip code


Address

1-3-1 Kajigaya Takatsu-ku Kawasaki Kanagawa

TEL

044-877-5111

Homepage URL


Email

hosa-p@toranomon.gr.jp


Sponsor or person

Institute

Toranomon Hospital

Institute

Department

Personal name



Funding Source

Organization

Toranomon Hospital

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



Other administrative information

Date of disclosure of the study information

2013 Year 09 Month 09 Day


Related information

URL releasing protocol


Publication of results

Unpublished


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

Enrolling by invitation

Date of protocol fixation

2013 Year 08 Month 21 Day

Date of IRB


Anticipated trial start date

2013 Year 09 Month 09 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 09 Month 06 Day

Last modified on

2017 Year 09 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000013639


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name