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NCT01796457 · ClinicalTrials.gov registry record

HBRN: Immune Regulation and Costimulation in Natural History and Therapeutic Outcome of Chronic Hepatitis B

A clinical trial of Hepatitis B, sponsored by University of Pennsylvania.

Active
Registry status
40
Enrollment target
8
Study locations

NCT01796457 is a study of Hepatitis B that is active but no longer recruiting, run by University of Pennsylvania. The registered enrollment target is 40 participants, below the 1,627-participant average among 32 other Hepatitis B trials with a reported enrollment target (98% lower). The trial reports 8 study locations across 6 states.

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The verdict

NCT01796457, a study of Hepatitis B, is active but no longer recruiting, sponsored by University of Pennsylvania.

ACTIVE NOT RECRUITING
Registry status
40 participants
Enrollment target
8
Study locations

Study Summary

This is an ancillary to the NIDDK-sponsored treatment trials titled: Combination Therapy of Pegylated Interferon Alfa-2a and Tenofovir Versus Tenofovir Monotherapy in Chronic Hepatitis B (NCT01369212) and Combination Entecavir and Peginterferon Therapy in HBeAg-Positive Immune-Tolerant Adults With Chronic Hepatitis B (NCT01369199). This study will examine the balance between immune regulatory and effector responses in hepatitis B-infected participants enrolled in the HBRN's clinical trials (NCT01369212 and NCT01369199) to define natural history and treatment outcome.

Conditions Studied

Study Locations (8)

California

  • California Pacific Medical Center - San Francisco
  • University of California San Francisco Medical Center - San Francisco

Washington

  • Virginia Mason Medical Center - Seattle
  • Harborview Medical Center - Seattle

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston

Minnesota

  • University of Minnesota - Plymouth

Virginia

  • Virginia Commonwealth University Medical Center - Richmond

Ontario

  • Toronto Western Hospital Liver Centre - Toronto

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-03
Est. Completion 2026-12-01

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT01796457

The ClinicalTrials.gov registry entry for NCT01796457 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,627-participant average among 32 other Hepatitis B trials with a reported enrollment target (98% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hepatitis B appearing as the primary indexed condition, and to 0 interventions.

NCT01796457 reports 8 study locations spanning 6 distinct geographic areas - top geographies include California, Washington, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01796457 about?

NCT01796457 is a clinical study titled "HBRN: Immune Regulation and Costimulation in Natural History and Therapeutic Outcome of Chronic Hepatitis B". This is an ancillary to the NIDDK-sponsored treatment trials titled: Combination Therapy of Pegylated Interferon Alfa-2a and Tenofovir Versus Tenofovir Monotherapy in Chronic Hepatitis B (NCT01369212) and Combination Entecavir and Peginterferon Therapy in HBeAg-Positive Immune-Tolerant Adults With C...

What is the current status of trial NCT01796457?

This trial is currently active not recruiting. The enrollment target is 40 participants. The study started on 2013-03. Estimated completion is 2026-12-01.

What conditions does trial NCT01796457 study?

This clinical trial studies the following conditions: Hepatitis B.

Who is sponsoring clinical trial NCT01796457?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01796457 being conducted?

This trial has 8 study locations across California, Massachusetts, Minnesota, Virginia, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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