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Terminated Phase 2 Interventional Results available

Evaluating the Safety and Effectiveness of Interferon-Free Treatment of Hepatitis C Virus Infection in HIV-Coinfected Adults on Antiretroviral Therapy

ClinicalTrials.gov ID: NCT02194998

Public ClinicalTrials.gov record NCT02194998. 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 Jul 21, 2026, 12:37 PM EDT

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

Official title

Interferon-Free Therapy for Chronic Hepatitis C Virus Genotype 1 Infection in Participants With HIV-1 Coinfection Receiving Concurrent Antiretroviral Therapy (C_ASCENT)

Study identification

NCT ID
NCT02194998
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
46 participants

Conditions and interventions

Interventions

  • Paritaprevir/ritonavir/ombitasvir (PTV/r/OBT) Drug
  • Dasabuvir (DSV) Drug
  • Ribavirin (RBV) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Sep 15, 2015
Primary completion
May 16, 2018
Completion
Nov 12, 2018
Last update posted
Nov 3, 2021

2015 – 2018

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Alabama CRS Birmingham Alabama 35294
UCLA CARE Center CRS Los Angeles California 90035
University of Colorado Hospital CRS Aurora Colorado 80045
Whitman-Walker Health CRS Washington D.C. District of Columbia 20005
Rush University CRS Chicago Illinois 60612
Johns Hopkins University CRS Baltimore Maryland 21205
New Jersey Medical School Clinical Research Center CRS Newark New Jersey 07103
Weill Cornell Chelsea CRS New York New York 10010
Cincinnati Clinical Research Site Cincinnati Ohio 45219
Penn Therapeutics, CRS Philadelphia Pennsylvania 19104
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213
The Miriam Hospital Clinical Research Site (TMH CRS) CRS Providence Rhode Island 02906
Trinity Health and Wellness Center CRS Dallas Texas 75208
Houston AIDS Research Team CRS Houston Texas 77030
University of Washington AIDS CRS Seattle Washington 98104-9929

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02194998, 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 Nov 3, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02194998 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →