Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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31 October 2016 |
Main ID: |
EUCTR2010-019843-20-DE |
Date of registration:
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09/08/2010 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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TMC435HPC3002 - 3-Year Follow up of Patients After Administration of TMC435 for the Treatment of Chronic Hepatitis C.
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Scientific title:
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A Prospective 3-Year Follow-up Study in Subjects Previously Treated in a Phase IIb or Phase III Study With a TMC435-Containing Regimen for the Treatment of Hepatitis C Virus (HCV) infection |
Date of first enrolment:
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Target sample size:
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250 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2010-019843-20 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no
Randomised: no
Open: no
Single blind: no
Double blind: no
Parallel group: no
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: no
Placebo: no
Other: no
Number of treatment arms in the trial: 0
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Phase:
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Human pharmacology (Phase I): no
Therapeutic exploratory (Phase II): no
Therapeutic confirmatory - (Phase III): yes
Therapeutic use (Phase IV): no
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Countries of recruitment
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Canada
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France
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Germany
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Poland
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Russian Federation
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United States
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Contacts
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Name:
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Janssen Biologics BV
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Address:
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Archimedesweg 29
2333CM
Leiden
Netherlands |
Telephone:
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+31071524 21 66 |
Email:
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ClinicalTrialsEU@its.jnj.com |
Affiliation:
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Janssen-Cilag International NV - Clinical Registry Group |
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Name:
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Janssen Biologics BV
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Address:
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Archimedesweg 29
2333CM
Leiden
Netherlands |
Telephone:
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+31071524 21 66 |
Email:
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ClinicalTrialsEU@its.jnj.com |
Affiliation:
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Janssen-Cilag International NV - Clinical Registry Group |
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Key inclusion & exclusion criteria
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Inclusion criteria: Have previously participated in a Phase II or Phase III study; received at least one dose of TMC435 in that study; completed the last patient visit of the previous study Are the trial subjects under 18? no Number of subjects for this age range: 0 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 42 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 2
Exclusion criteria: Currently enrolled or plan to enroll in another study with an investigational drug or invasive investigational medical device; received antiviral or immunomodulating treatment for HCV between last visit previous study and this study
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Hepatitis C Virus (HCV) MedDRA version: 16.1
Level: LLT
Classification code 10019752
Term: Hepatitis C virus (HCV)
System Organ Class: 100000004848
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Therapeutic area: Diseases [C] - Virus Diseases [C02]
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Intervention(s)
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Pharmaceutical Form:
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Primary Outcome(s)
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Main Objective: - To evaluate the durability of sustained virologic response (SVR) in subjects who were treated with a TMC435- containing regimen in a previous Phase IIb or Phase III study and maintained undetectable HCV ribonucleic acid (RNA) until the last planned visit of that previous study (LPVPS). - To evaluate sequence changes in the HCV NS3/4A region over time in subjects who were treated with a TMC435-containing regimen in a previous Phase IIb or Phase III study and had confirmed detectable HCV RNA at the LPVPS.
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Primary end point(s): - Proportion (%) of patients with undetectable HCV RNA (<25 IU/mL undetectable) - Change in sequence of HCV NS3/4A region over time in patients with confirmed detectable HCV RNA at the last visit of the previous study
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Secondary Objective: - To assess the frequency of late relapse (i.e., relapse at any time after the LPVPS until the last individual visit of the present study) and evaluate sequence changes in the HCV NS3/4A region in subjects with late relapse (i.e., subjects with SVR and undetectable HCV RNA at the LPVPS and subsequent relapse). - To assess the development of liver disease progression in subjects previously treated with a TMC435-containing regimen.
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Timepoint(s) of evaluation of this end point: Every six months, starting at six months after the last patient visit of the previous study, and up to three years after the last visit of the previous study
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Secondary Outcome(s)
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Timepoint(s) of evaluation of this end point: - Every six months, starting at six months after the last patient visit of the previous study, and up to three years after the last visit of the previous study
- Starting at screening, and then every six months, starting at six months after the last patient visit of the previous study, and up to three years after the last visit of the previous study
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Secondary end point(s): - Change in sequence of the HCV NS3/4A region in patients with late relapse, i.e. relapse after the last visit of the previous study
- Development of liver disease progression in patients previously treated with a TMC435-containing regimen
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Secondary ID(s)
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TMC435HPC3002
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Source(s) of Monetary Support
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Janssen R&D Ireland
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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