Unique ID issued by UMIN | UMIN000020301 |
---|---|
Receipt number | R000023439 |
Scientific Title | A Study on Predictors of Treatment Response to daclatasvir and Asunaprevir combination therapy in Patients with genotype 1 Chronic Hepatitis C Virus Infection |
Date of disclosure of the study information | 2015/12/21 |
Last modified on | 2019/06/24 15:48:41 |
A Study on Predictors of Treatment Response to daclatasvir and Asunaprevir combination therapy in Patients with genotype 1 Chronic Hepatitis C Virus Infection
Predictor of treatment response to DCV/ASV therapy
A Study on Predictors of Treatment Response to daclatasvir and Asunaprevir combination therapy in Patients with genotype 1 Chronic Hepatitis C Virus Infection
Predictor of treatment response to DCV/ASV therapy
Japan |
Patients with genotype 1 HCV infection
Hepato-biliary-pancreatic medicine |
Others
NO
To evaluate the efficacy and safety of daclatasvir plus asnaprevir combination therapy in patients with a chronic HCV genotype 1 infection, and investigate predictors of treatment response based on the analyses of viral and host factors
Safety,Efficacy
To investigate the predictors obtained at baseline and affecting the sustained virologic response (SVR) rate/occurrence of adverse drug reactions at follow-up Week 12
Observational
20 | years-old | <= |
Not applicable |
Male and Female
Patients (1) with the target disease who (2) satisfy all the inclusion criteria and (3) meet none of the exclusion criteria are eligible for the study.
(1) Subjects
Patients with a chronic HCV infection and compensated cirrhosis who are being treated as outpatients or inpatients at institutions participating in this study
(2) Inclusion criteria
[1] Patients who are 20 years of age or older at the time of informed consent
[2] Patients who have been fully informed and have provided written informed consent to participate in this study prior to study initiation
[3] Patients with a chronic HCV genotype 1 infection and compensated cirrhosis who do not meet any of the following exclusion criteria
1) Patients with poorly controlled cardiac disease (e.g., myocardial infarction, cardiac failure, arrhythmia)
2) Patients with severe hepatic impairment
3) Patients with a history of hypersensitivity to HCV protease inhibitors or NS5A inhibitor
4) Patients with a concurrent malignancy, including hepatocellular carcinoma, at the start of treatment
5) Patients deemed unsuitable for study entry by their treating physician
6) Patients who are unsuitable, in the opinion of the principal investigator, for this study due to any other reason
140
1st name | Goki |
Middle name | |
Last name | Suda |
Hokkaido University
Department of Gastroenterology and Hepatology, Graduate School of Medicine,
0650010
Kita 14-jo Nishi 5-jo, Kita-ku, Sapporo city, Hokkaid
+81-11-716-1161
gsudgast@pop.med.hokudai.ac.jp
1st name | Goki |
Middle name | |
Last name | Suda |
Hokkaido University
Department of Gastroenterology and Hepatology, Graduate School of Medicine,
0650010
Kita 14-jo Nishi 5-jo, Kita-ku, Sapporo city, Hokkaid
+81-11-716-1161
gsudgast@pop.med.hokudai.ac.jp
Hokkaido University
Bristol-Myers Squibb
Profit organization
IRB committee of Hokkaido University Hospital
Kita 14 zyou nishi-5tyoume kitaku sapporo city
011-706-7636
crjimu@huhp.hokudai.ac.jp
NO
北海道大学病院(北海道)
2015 | Year | 12 | Month | 21 | Day |
Unpublished
Completed
2014 | Year | 07 | Month | 08 | Day |
2014 | Year | 07 | Month | 08 | Day |
2014 | Year | 07 | Month | 08 | Day |
2018 | Year | 03 | Month | 31 | Day |
This study is cohort study
Way for subscription
Patients who visit our hospital between July 2014 and march 2017, and meet inclusion criteria are enrolled.
2015 | Year | 12 | Month | 21 | Day |
2019 | Year | 06 | Month | 24 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023439