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NCT03122132: 3D8

Effectiveness, Safety and Clinical Outcomes of Paritaprevir/Ombitasvir/r+Dasabuvir 8 Weeks

Completed Last updated 21 May 2018
What this trial tests

trial testing ombitasvir/paritaprevir/ritonavir 8 weeks in Hepatitis C Infection in 200 participants. Completed in 1 March 2018.

Timeline
20 February 2017
Primary endpoint
1 January 2018
1 March 2018

Quick facts

Lead sponsorHepa C
StatusCompleted
Study typeOBSERVATIONAL
Enrollment200
Start date20 February 2017
Primary completion1 January 2018
Estimated completion1 March 2018
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Hepa C — full company profile →

Who can join

18 and older, any sex, with Hepatitis C Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to evaluate in clinical practice the efficacy and safety of ombitasvir/paritaprevir/ ritonavir and dasabuvir administered for 8 weeks in treatment-naïve participants with genotype 1b hepatitis C virus (HCV).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Eight weeks of Paritaprevir/r/Ombitasvir + Dasabuvir in HCV genotype 1b with mild-moderate fibrosis: Results from a real-world cohort.
    Puigvehí M, De Cuenca B, Viu A, Diago M, et al · · 2019 · cited 3× · PMID 30160363 · DOI 10.1111/liv.13950

Verify or expand the search:

Other recruiting trials for Hepatitis C Infection

Currently open trials in the same condition.

Other Hepa C trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03122132.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing