UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000015247 |
|---|---|
| Receipt number | R000017728 |
| Scientific Title | Efficacy and safety of daclatasvir and asunaprevir in patients with chronic hepatitis C |
| Date of disclosure of the study information | 2014/09/25 |
| Last modified on | 2019/08/02 15:43:22 |
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Basic information
Public title
Efficacy and safety of daclatasvir and asunaprevir in patients with chronic hepatitis C
Acronym
Efficacy and safety of daclatasvir and asunaprevir
Scientific Title
Efficacy and safety of daclatasvir and asunaprevir in patients with chronic hepatitis C
Scientific Title:Acronym
Efficacy and safety of daclatasvir and asunaprevir
Region
| Japan |
Condition
Condition
Patients with chronic hepatitis C virus infection
Classification by specialty
| Medicine in general | Hepato-biliary-pancreatic medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To assessment of efficacy and safety of daclatasvir and asunaprevir in patients with chronic hepatits C.
To investigate the relative factor with antiviral effect, emergence of drug-resistant virus and the suppressive effect for incidence of hepatocellular carcinoma.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Sustained virologic response rate
The factor associated with sustained virologic response
Safety
Emergence of drug-resistant virus
Cumulative incidence of hepatocellular carcinoma
The factor associated with incidence of hepatocellular carcinoma
Key secondary outcomes
Base
Study type
Observational
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
Interventions/Control_2
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
1) Patients with 20 years of age and older
2) Chronic hepatitis or cirrhosis patients with HCV serogroup 1
3) Ineligible or intorelant patients, or non-responder for antiviral therapy including interferon
4) Eligible patients for daclatsvir and asunaprevir
Key exclusion criteria
1) Co-infection with hepatitis B virus
2) Co-infection with anti-human immunodeficiency virus
3) Other forms of liver disease (alcohol liver disease, autoimmune hepatitis etc.)
4) Decompensated cirrhosis, Liver failure
5) Severe multisystem disease, Severe immunodeficiency
6) Pregnant woman
7) Contraindication to daclatasvir and asunaprevir
Target sample size
350
Research contact person
Name of lead principal investigator
| 1st name | Tetsuo |
| Middle name | |
| Last name | Takehara |
Organization
Osaka University Graduate School of Medicine
Division name
Gastroenterology and Hepatology
Zip code
565-0871
Address
2-2, Yamadaoka, Suita, Osaka, Japan
TEL
81-6-6879-3621
takehara@gh.med.osaka-u.ac.jp
Public contact
Name of contact person
| 1st name | Ryotaro |
| Middle name | |
| Last name | Sakamori |
Organization
Osaka University Graduate School of Medicine
Division name
Gastroenterology and Hepatology
Zip code
565-0871
Address
2-2, Yamadaoka, Suita, Osaka, Japan
TEL
81-6-6879-3621
Homepage URL
sakamori@gh.med.osaka-u.ac.jp
Sponsor or person
Institute
Osaka University Graduate School of Medicine, Department of Gastroenterology and Hepatology
Institute
Department
Personal name
Funding Source
Organization
Grant-in-Aid for Research on Hepatitis from Ministry of Health Labour and Welfare of Japan, and Scientific Research from the Ministry of Education, Science, and Culture of Japan
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Osaka University Clinical Research Review Committee
Address
2-2, Yamadaoka, Suita, Osaka
Tel
06-6210-8289
rinri@hp-crc.med.osaka-u.ac.jp
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
| 2014 | Year | 09 | Month | 25 | 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
No longer recruiting
Date of protocol fixation
| 2014 | Year | 09 | Month | 17 | Day |
Date of IRB
Anticipated trial start date
| 2014 | Year | 09 | Month | 25 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
frequencies of RA in non-SVR patients
Management information
Registered date
| 2014 | Year | 09 | Month | 25 | Day |
Last modified on
| 2019 | Year | 08 | Month | 02 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000017728
