Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03059446 · ClinicalTrials.gov registry record · Phase 2

Rollover Study of Cenicriviroc for the Treatment of Liver Fibrosis in Participants With Nonalcoholic Steatohepatitis

A Phase 2 study, sponsored by Tobira Therapeutics.

Terminated
Registry status
Phase 2
Development phase
167
Enrollment target

NCT03059446: Clinical Trial Phase 2 study, sponsored by Tobira Therapeutics.

NCT03059446 is a Phase 2 study that was terminated before completion, run by Tobira Therapeutics. The registered enrollment target is 167 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03059446, a Phase 2 study, was terminated before completion, sponsored by Tobira Therapeutics.

TERMINATED
Registry status
Phase 2
Development phase
167 participants
Enrollment target

Study Summary

This rollover study will provide open-label treatment with cenicriviroc and will assess the long-term safety of continued treatment with cenicriviroc in participants who participated in either the CENTAUR study 652-2-203 \[NCT02217475\] or the AURORA study \[NCT03028740\].

Primary Outcome

An AE is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have a causal relationship with the treatment. A treatment-emergent AE is an AE that occurs after a participant receives study drug.

Interventions

  • DRUG Cenicriviroc

Trial Details

FieldValue
Enrollment Target 167 participants
Start Date 2017-02-14
Est. Completion 2021-01-05
Phase Phase 2
Tobira Therapeutics

11 total trials

Why NCT03059446 stopped before completion

NCT03059446 is an interventional study that assigns participants to a tested intervention. The registered 167 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% higher).

The record links to 0 conditions, and to 1 intervention - of which Cenicriviroc is the first listed.

NCT03059446 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03059446 about?

NCT03059446 is a clinical study titled "Rollover Study of Cenicriviroc for the Treatment of Liver Fibrosis in Participants With Nonalcoholic Steatohepatitis". This rollover study will provide open-label treatment with cenicriviroc and will assess the long-term safety of continued treatment with cenicriviroc in participants who participated in either the CENTAUR study 652-2-203 \[NCT02217475\] or the AURORA study \[NCT03028740\].

What is the current status of trial NCT03059446?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 167 participants. The study started on 2017-02-14. Estimated completion is 2021-01-05.

What interventions are being tested in trial NCT03059446?

The interventions under investigation include: Cenicriviroc (DRUG).

Who is sponsoring clinical trial NCT03059446?

This trial is sponsored by Tobira Therapeutics, which has 11 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03059446's enrollment target sits among peer trials

167 406th of 2000 higher than 1,595 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04248283 · 167 participants · NA

    Adjustable Continence Therapy (ACT) for the Treatment of Female SUI

  • NCT04552509 · 167 participants · NA

    TRUEBEAM Stereotactic Body Radiotherapy for Localized Prostate Cancer

  • NCT05516277 · 167 participants · NA

    Insomnia Treatment and Cardiometabolic Health in Older Adults With Posttraumatic Stress Disorder

  • NCT02118922 · 168 participants

    A Study to Test the Diagnostic Potential of Brillouin Microscopy for Corneal Ectasia

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03059446, the US trial registry maintained by the National Library of Medicine. NCT03059446 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.