NCT Number: NCT00262483
Phase 2 Study of VX-950, Pegasys and Copegus in Hepatitis C
To assess the safety of the combination of VX-950, Pegasys and Copegus in subjects with hepatitis C.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Call for information, Santurce, Puerto Rico
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Infected with hepatitis C virus
Exclusion criteria
- Contraindications to peginterferon or ribavirin therapy.
Treatment and study plan
Ribavirin
DrugPeginterferon alfa-2a
DrugPrimary outcomes
-
Safety of triple combination therapy.
Time frame: retrospective and prospective
Secondary outcomes
-
Pharmacokinetics of VX-950, peginterferon alfa-2a and ribavirin.
Time frame: retrospective and prospective
-
Plasma HCV RNA levels
Time frame: retrospective and prospective
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Lead sponsor
Vertex Pharmaceuticals Incorporated
Industry
Registry information
Official study title
A Phase 2 Study of VX-950 in Combination With Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Subjects With Hepatitis C
Important dates
- Study start
- 2005
- Study completion
- 2006
- First posted
- Dec 6, 2005
- Registry last updated
- Dec 21, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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