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Influence of Nevirapine on HCV Viral Load

Influence of Nevirapine on HCV Viral Load Among HIV/HCV-coinfected Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01277627
Acronym
HELICON
Enrollment
60
Registered
2011-01-17
Start date
2011-01-31
Completion date
Unknown
Last updated
2011-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCV Infection., HCV Viral Load.

Keywords

HCV, HIV, Nevirapine, HCV viral load, Efavirenz, Protease inhibitors

Brief summary

Nevirapine-based antiretroviral therapy is associated with lower plasma HCV viral load in HIV/HCV-coinfected individuals.

Interventions

DRUGNevirapine

nevirapine: 400 mg a day.

DRUGefavirenz, protease inhibitors

efavirenz: 600 mg a day

Sponsors

Boehringer Ingelheim
CollaboratorINDUSTRY
Valme University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* HIV infection. * Older than 18 years. * Chronic hepatitis C. * Undetectable HIV viral load during one year before starting study. * To have not received HCV therapy during one year before starting study. * To have not started efavirenz or protease inhibitors o nucleoside analogs during 6 months before starting study. * Non contraindications for drugs included in this study. * To change an antiretroviral regimen including efavirenz or protease inhibitors by nevirapine due to side effects, interactions or pregnancy (NVP group) * To continue with a antiretroviral regimen including efavirenz or protease inhibitors (non-NVP group) Both groups will be matched according to these variables: * Liver stiffness. * HCV genotype. * Hospital. * Time from starting antiretroviral therapy. * Previous third drug (EFV or PI) to introduction of NVP.

Exclusion criteria

* HCV therapy during follow-up

Design outcomes

Primary

MeasureTime frame
Changes in HCV viral load48 weeks

Countries

Spain

Contacts

Primary ContactJOSE MIRA-ESCARTI, M.D
miraescarti@yahoo.es+34-955015363

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026