Last reviewed · How we verify
NCT03122132: 3D8
Effectiveness, Safety and Clinical Outcomes of Paritaprevir/Ombitasvir/r+Dasabuvir 8 Weeks
trial testing ombitasvir/paritaprevir/ritonavir 8 weeks in Hepatitis C Infection in 200 participants. Completed in 1 March 2018.
1 January 2018
Quick facts
| Lead sponsor | Hepa C |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 200 |
| Start date | 20 February 2017 |
| Primary completion | 1 January 2018 |
| Estimated completion | 1 March 2018 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- ombitasvir/paritaprevir/ritonavir 8 weeks — full drug profile →
- dasabuvir 8 weeks — full drug profile →
Conditions studied
- Hepatitis C Infection — all drugs for Hepatitis C Infection →
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):
-
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:
- PubMed search for NCT03122132
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hepatitis C Infection
Currently open trials in the same condition.
- NCT02772003 — DNA Vaccine Therapy in Treating Patients With Chronic Hepatitis C Virus Infection · Phase 1 · active not recruiting
Other Hepa C trials
Trials by the same sponsor.
- NCT03111966 — Effectiveness, Safety and Clinical Outcomes of Elbasvir/Grazoprevir: Results From a Spanish Real World Cohort · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03122132 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hepa C
- Last refreshed: 21 May 2018
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