Hôpital Tenon Service des Maladies Infectieuses
Paris, 75970, France
NCT Number: NCT00901524
The purpose of this study is to assess the effectiveness of an optimized anti HCV treatment (360μg per week of PegIFN-alpha2a + 18mg/kg/j of Ribavirin for 6 months.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 2
Paris, 75970, France
In patients HIV infected, the success rate do not exceed 20% in genotype 1 or 4 patients. In case of treatment failure , patients are rarely re-treated, and liver fibrosis progresses rapidly. The new molecules are not yet available for patients co-infected with HIV, and patients having already undergone a first treatment will likely be among the last to be included in trials evaluating the effectiveness of these treatments.
However, recent studies show that it is possible to propose a new treatment "optimized" to these patients in the hope to obtain better success rate. Provide antiretroviral treatment, use of high doses of Peg-interferon and ribavrine, and supporting patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pilot study, multicenter, open label
Time frame: W72 or W96 (depending of the end of treatment)
Time frame: W4 and W12
ANRS, Emerging Infectious Diseases
Other Gov
ANRS HC20 Pilot Study, Multicenter, Assessing the Effectiveness of an Optimized Anti HCV (360μg/Week Induction of PegIFN-alpha2a + 18mg/kg/j of RBV for 6 Months and Then Depending on the Virological Response to S12, Elongation up S72 to the Dual Anti HCV, With Accompanying Measures) on Sustained Virological Response in Patients With HCV Genotype 1 and 4 Non Responders and Co-infected With HIV.
Acronym: ETOC
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.
Published trials that share one or more normalized conditions with this study.
NCT04593355
Blood-Borne Infections, Communicable Diseases
Changchun, Jilin, China
View Trial DetailsNCT02103439
Blood-Borne Infections, Communicable Diseases
Kazan', Tatarstan Republic, Russia
View Trial DetailsNCT01889433
Blood-Borne Infections, Communicable Diseases
Homyel, Belarus
View Trial DetailsNCT03482388
Behavior, Blood-Borne Infections
Guangzhou, China
View Trial Details