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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02753699




Registration number
NCT02753699
Ethics application status
Date submitted
16/03/2016
Date registered
28/04/2016
Date last updated
26/08/2016

Titles & IDs
Public title
Long Term Follow-up Study to Assess Durability of Sustained Virologic Response in Alisporivir-treated Hepatitis C Patients
Scientific title
A Multi-centre Long Term Follow-up Study to Assess the Durability of Sustained Virologic Response in Alisporivir-treated Chronic Hepatitis C Patients
Secondary ID [1] 0 0
2011-006131-38
Secondary ID [2] 0 0
CDEB025A2312
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hepatitis C 0 0
Condition category
Condition code
Infection 0 0 0 0
Other infectious diseases
Oral and Gastrointestinal 0 0 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Alisporivir

Experimental: From Study 2210 - All participants enrolled from CDEB025A2210 (n=164) who had been treated with alisporivir during the feeder study. There was no investigational treatment given to participants while enrolled in this follow-up study.

Experimental: From Study 2301 - All participants enrolled from CDEB025A2301 (n=397) who had been treated with alisporivir during the feeder study. There was no investigational treatment given to participants while enrolled in this follow-up study.

Experimental: From Study 2211 - All participants enrolled from CDEB025A2211 (n=162) who had been treated with alisporivir during the feeder study. There was no investigational treatment given to participants while enrolled in this follow-up study.


Treatment: Drugs: Alisporivir
Intervention of interest; follow-up after ALV-active study
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of Participants Maintaining Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) Load Below the Level of Quantification (LOQ) Through Week 48
Timepoint [1] 0 0
up to 120 Weeks
Secondary outcome [1] 0 0
Percentage of Participants With Normal Alanine-aminotransferase (ALT) Values at Week 48.
Timepoint [1] 0 0
at Week 48

Eligibility
Key inclusion criteria
1. Provides written informed consent before any assessment is performed
2. Is male or female aged =18
3. Has previously completed a Novartis-sponsored hepatitis C study and received alisporivir
4. Has achieved SVR24
5. Is able to comply with the visit schedule
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Use of any investigational drugs within 5 half-lives of enrollment, or within 30 days of that medication, whichever is longer.
2. Use or planned use to start a new course of hepatitis C therapy.
3. No additional exclusions are to be applied by the Investigator, in order to ensure that the study population is representative of all eligible patients.

Study design
Purpose of the study
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/12/2011
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/05/2015
Sample size
Target
Accrual to date
Final
723
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
Recruitment hospital [1] 0 0
Novartis Investigative Site - Kingswood
Recruitment hospital [2] 0 0
Novartis Investigative Site - Kogarah
Recruitment hospital [3] 0 0
Novartis Investigative Site - Westmead
Recruitment hospital [4] 0 0
Novartis Investigative Site - Greenslopes
Recruitment hospital [5] 0 0
Novartis Investigative Site - Fitzroy
Recruitment postcode(s) [1] 0 0
2747 - Kingswood
Recruitment postcode(s) [2] 0 0
2217 - Kogarah
Recruitment postcode(s) [3] 0 0
2145 - Westmead
Recruitment postcode(s) [4] 0 0
4120 - Greenslopes
Recruitment postcode(s) [5] 0 0
3065 - Fitzroy
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Florida
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United States of America
State/province [3] 0 0
Hawaii
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United States of America
State/province [4] 0 0
Illinois
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United States of America
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Indiana
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United States of America
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Texas
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United States of America
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Utah
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Argentina
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Buenos Aires
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Belgium
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Gent
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Canada
State/province [10] 0 0
Alberta
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Canada
State/province [11] 0 0
British Columbia
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Canada
State/province [12] 0 0
Ontario
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France
State/province [13] 0 0
Clichy
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France
State/province [14] 0 0
Creteil
Country [15] 0 0
France
State/province [15] 0 0
Lyon Cedex 04
Country [16] 0 0
France
State/province [16] 0 0
Nice Cedex 3
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France
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Paris
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Germany
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Berlin
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Germany
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Frankfurt
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Germany
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Freiburg
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Germany
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Hamburg
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Germany
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Hannover
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Germany
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Kiel
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Germany
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Koeln
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Germany
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Leipzig
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Germany
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Mainz
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Hong Kong
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Hong Kong
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Hungary
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Bekescsaba
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Hungary
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Budapest
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Hungary
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Debrecen
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Hungary
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Kaposvár
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Hungary
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Pecs
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Hungary
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Szekesfehervar
Country [34] 0 0
India
State/province [34] 0 0
Andhra Pradesh
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India
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Maharashtra
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India
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Punjab
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India
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Delhi
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Italy
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BO
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Italy
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BS
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Italy
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MI
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Italy
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PA
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Italy
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PR
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Italy
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PV
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Italy
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RM
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Italy
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TO
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Italy
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Bologna
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Italy
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Napoli
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Korea, Republic of
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Gyeonggi-do
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Korea, Republic of
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Gyeongsangnam-Do
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Korea, Republic of
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Korea
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Korea, Republic of
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Busan
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Korea, Republic of
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Incheon
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Korea, Republic of
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Pusan
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Mexico
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Distrito Federal
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Mexico
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Nuevo Leon
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Poland
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Bialystok
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Poland
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Bydgoszcz
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Poland
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Lódz
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Poland
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Warszawa
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Poland
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Zawiercie
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Romania
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Bucharest
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Romania
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Craiova
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Romania
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Iasi
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Russian Federation
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Moscow
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Russian Federation
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St.- Petersburg
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Spain
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Andalucia
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Spain
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Catalunya
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Spain
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Comunidad Valenciana
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Spain
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Madrid
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Taiwan
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Chia-Yi
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Taiwan
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Kaohsiung
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Taiwan
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Keelung City
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Taiwan
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Lin-Kou
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Taiwan
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Niaosong Township
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Taiwan
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Taichung
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Taiwan
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Taipei
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Taiwan
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Yun-Lin
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Thailand
State/province [78] 0 0
Bangkok
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Thailand
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Chiang Mai
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Thailand
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Khon Kaen
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Thailand
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Songkla
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Turkey
State/province [82] 0 0
Fatih / Istanbul
Country [83] 0 0
Turkey
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Izmir
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United Kingdom
State/province [84] 0 0
Birmingham
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United Kingdom
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Glasgow - Scotland
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United Kingdom
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London
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United Kingdom
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Newcastle Upon Tyne
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United Kingdom
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Nottingham
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United Kingdom
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Plymouth
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Vietnam
State/province [90] 0 0
Hanoi
Country [91] 0 0
Vietnam
State/province [91] 0 0
Ho Chi Minh

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Debiopharm International SA
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Novartis Pharmaceuticals
Address 0 0
Novartis Pharmaceuticals
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT02753699