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Clinical trial

Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P (TARGET3D)

Read time: 3 mins
Last updated:1st Jun 2016
Identifier: NCT02634008

Brief Summary:
An open label, multicentre, international pilot study of paritaprevir/ritonavir, ombitasvir, dasabuvir with or without ribavirin or glecaprevir/pibrentasvir for people with recently acquired hepatitis C virus infection with or without HIV co-infection.

Detailed Description:
The use of a highly potent IFN-sparing drug combination in the setting of recently acquired 1 HCV infection is hypothesised to result in the vast majority of patients achieving SVR. In this setting, it is anticipated that therapy can be shortened relative to that used in established chronic infection. A short course IFN-free strategy is likely to be highly attractive to both patients and clinicians and if proven may further encourage early HCV testing and diagnosis.

In this pilot study, the investigators plan to explore the safety, efficacy and feasibility of the IFN-sparing combination for treatment of recently acquired HCV infection.

Cohort One: paritaprevir/ritonavir/ombitasvir, dasabuvir with/without ribavirin (HCV genotype 1 only) Cohort Two (and Three): glecaprevir/pibrentasvir (HCV genotypes 1-6)

Study Type: Interventional  (Clinical Trial)
Estimated Enrollment: 90 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open Label, Multicentre, International Pilot Study of Paritaprevir/Ritonavir, Ombitasvir, Dasabuvir With or Without Ribavirin or Glecaprevir/Pibrentasvir for People With Recently Acquired Hepatitis C Virus Infection With or Without HIV Co-infection.
Actual Study Start Date: June 2016
Estimated Primary Completion Date: June 2019
Estimated Study Completion Date: December 2022

- Experimental:
Cohort 1
Paritaprevir/ritonavir/ombitasvir (75mg/50mg/12.5mg) and dasabuvir (250mg) with or without ribavirin (1000-1200mg) daily taken orally for 8 weeks.
- Experimental: Cohort 2
Three tablets of glecaprevir/pibrentasvir (100mg/40mg) daily taken orally for 6 weeks
- Experimental: Cohort 3
Three tablets of glecaprevir/pibrentasvir (100mg/40mg) daily taken orally for 4 weeks

Category Value
Date last updated at source 2018-08-08
Study type(s) Interventional
Expected enrolment 90
Study start date 2016-06-01
Estimated primary completion date 2019-06-01

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