A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With or Without Ribavirin (RBV) in Adults With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection
Study Identifier
M14-423
CT.gov Identifier
EudraCT Identifier
EUCTIS ID
Not available
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Study Complete
Results Available
Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English
Scientific Result Summary
Available Language(s): English
Plain Language Summary
Available Language(s): English, French, Dutch, Portuguese (Native), Italian, Turkish
Study Details
Medical Condition
Study Drug
Phase
Phase 3
Sex
Female & Male
Age
18 - 99 Years
Protocol Summary
The purpose of this study was to evaluate the effect of treatment with ABT-450 co-formulated with ritonavir and ABT-267 (ABT-450/r/ABT-267) and ABT-333; 3-DAA regimen, with or without ribavirin (RBV) in adults with chronic hepatitis C virus genotype 1 (HCV GT1) infection.
Study Locations
Location
Status
Location
CHU Bab El Oued /ID# 145420
Algiers, Algeria, 16000
Status
Not applicable
Location
CHU Bologhine Hospital /ID# 145421
Algiers, Algeria, 16000
Status
Not applicable
Location
CHU Mustapha Bacha /ID# 132130
Algiers, Algeria, 16000
Status
Not applicable
Location
St Vincent's Hospital Sydney /ID# 131001
Darlinghurst, New South Wales, Australia, 2010
Status
Not applicable
Location
Nepean Hospital /ID# 130999
Kingswood, New South Wales, Australia, 2747
Status
Not applicable
Location
Westmead Hospital /ID# 130997
Westmead, New South Wales, Australia, 2145
Status
Not applicable
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