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Completed Phase 2 Interventional Results available

Alisporivir With RBV in Chronic Hepatitis C Genotype 2 and 3 Participants for Whom Interferon is Not an Option

ClinicalTrials.gov ID: NCT02094443

Public ClinicalTrials.gov record NCT02094443. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 22, 2026, 9:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Open-label, Randomized, 2-arm, Phase II Trial of Pharmacodynamics, Pharmacokinetics and Safety of Two Dose Regimens of DEB025/Alisporivir in Combination With Ribavirin Therapy in Chronic Hepatitis C Genotype 2 and 3 Patients Who Have Previously Failed Interferon Therapy or Are Intolerant or Unable to Take Interferon.

Study identification

NCT ID
NCT02094443
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Debiopharm International SA
Industry
Enrollment
52 participants

Conditions and interventions

Interventions

  • Alisporivir Drug
  • Ribavirin Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2014
Primary completion
Mar 31, 2015
Completion
Mar 31, 2015
Last update posted
Oct 12, 2016

2014 – 2015

United States locations

U.S. sites
11
U.S. states
5
U.S. cities
9
Facility City State ZIP Site status
Novartis Investigative Site Bakersfield California 93301
Novartis Investigative Site Lancaster California 93534
Novartis Investigative Site San Diego California 92114
Novartis Investigative Site San Diego California 92128
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Arlington Texas 76012
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site San Antonio Texas 78215
Novartis Investigative Site Newport News Virginia 23602
Novartis Investigative Site Seattle Washington 98101
Novartis Investigative Site Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02094443, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 12, 2016 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02094443 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →