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Severe Hepatitis Intervention With Emapalumab for Liver Disease (SHIELD)

31. Juli 2026 aktualisiert von: Children's Healthcare of Atlanta

A Phase 2 Study of Emapalumab for Prevention of Liver Failure in Pediatric Indeterminate Severe Hepatitis Associated With T-Cell Activation: Severe Hepatitis Intervention With Emapalumab for Liver Disease

The goal of this study is to see whether a medicine called emapalumab, a monoclonal antibody, is safe and works well for patients aged 1 year and older who have indeterminate severe hepatitis with T-cell activation and have not responded well to steroids or still need them.

This study has a Screening Cohort and an Intervention Cohort.

The Screening Cohort will enroll patients with severe hepatitis of all etiologies to observe and collect research samples. Patients enrolled on the Screening Cohort will be asked to participate on the Intervention Cohort if they develop steroid-refractory/ dependent indeterminate severe hepatitis (iSH-T). Additionally, patients may bypass the Screening Cohort and enroll directly in the Intervention Cohort if they already meet its eligibility criteria. Patients in the Intervention Cohort will be treated with emapalumab.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

This clinical protocol evaluates the use of emapalumab, an anti-IFN-γ monoclonal antibody, in children aged ≥1 year with steroid-refractory or steroid-dependent indeterminate severe hepatitis with T cell activation (iSH-T). This study aims to establish a safe and effective treatment pathway for a previously steroid-refractory/dependent subjects with iSH-T.

Pediatric severe acute hepatitis is a rare but serious disorder that can rapidly progress to liver failure. Previously healthy children who develop severe acute hepatitis can unpredictably progress to pediatric acute liver failure (PALF) over the course of days to weeks. Importantly, as many as 30-50% of all PALF cases have no specific causal etiology for their liver failure and are termed indeterminate PALF (iPALF) and are at the highest risk for liver transplantation. Work from the PALF study group investigators has identified that iPALF is a leading indication for liver transplantation in children. Additional investigation indicates that iPALF patients have significant T cell activation and CD8+ T cell infiltration of their hepatic tissue. There are reports using immunosuppression in iPALF and PALF with favorable results and it is also the subject of a current multicenter trial in children (NCT04862221).

Studientyp

Interventionell

Einschreibung (Geschätzt)

28

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria (Screening Cohort):

  • Age: Participants must be ≥ 1 year of age at the time of screening.
  • Evidence of Severe Hepatic Injury of all etiology (not just iSH/ iSH-T): Serum alanine aminotransferase (ALT) ≥ 1000 U/L documented within 7 days prior to enrollment.

Exclusion Criteria (Screening Cohort):

  • Any condition impairing informed consent/assent or protocol compliance

Inclusion Criteria (Intervention Cohort; patients who meet Intervention Cohort eligibility can bypass Screening Cohort enrollment):

  • Steroid-refractory, steroid-dependent, or relapse of hepatitis after stopping steroids and have an Indeterminate etiology of hepatitis based on standard of care, age appropriate evaluation
  • Age: ≥ 1 year
  • ALT ≥ 1000 U/L prior to initiation of any immune modulatory therapy
  • Evidence of T-cell activation at initial diagnosis, as indicated by one of the following:

    • sIL2R > 2× upper limit of normal (ULN)
    • CXCL9 > 5× ULN
    • CD8+ T-cell infiltration in the liver
  • INR < 2.0 without evidence of hepatic encephalopathy

Exclusion Criteria (Intervention Cohort; patients who meet Intervention Cohort eligibility can bypass Screening Cohort enrollment):

  • Patients with known Liver failure (defined as INR >2 on two consecutive occasions without hepatic encephalopathy (HE), or INR ≥1.5 with evidence of HE)
  • Evidence of chronic liver disease or parenchymal nodularity as demonstrated on imaging (US, CT, or MRI)
  • Evidence of hepatic encephalopathy
  • Severe acquired aplastic anemia at presentation
  • Organ dysfunction assessment defined below:

    • Renal dysfunction: eGFR < 30 mL/min/1.73m² or
    • Mechanical Ventilation
  • Persistent systemic infection despite appropriate antimicrobial therapy
  • Active infection with Hepatitis A, B, C, HIV, or herpes simplex virus
  • Active mycobacteria (typical and atypical), Histoplasma Capsulatum, Herpes zoster infections.
  • Patients with positive respiratory viral infection, including adenovirus, rhinovirus/enterovirus, SARS-CoV-2, influenza, and respiratory syncytial virus, only if they also have declining respiratory function needing positive pressure support. Suspected primary hemophagocytic lymphohistiocytosis based on patients with a history of consanguinity and/or central nervous system dysfunction or other clinical manifestations that is exaggerated compared to the degree of liver dysfunction (as judged by the site investigator and study team)
  • Diagnosis of Autoimmune Hepatitis, Wilson Disease, inborn error of metabolism, acute drug or toxin-induced liver injury, or ischemic liver injury
  • History of severe hypersensitivity or allergy to any component of this study regimen
  • History of confirmed malignancy
  • History of recreational drug use within the past 4 weeks, excluding cannabinoids
  • Therapy with an immunosuppressive agent or an experimental drug within the past 6 weeks
  • Pregnant, planning to become pregnant during study window, or breastfeeding at time of study entry
  • Patients of reproductive potential are not eligible unless they have agreed to use an effective contraceptive method (e.g. hormonal contraceptives, intrauterine device, or double-barrier method) for the duration of their study participation. Patients must maintain adequate contraception for at least 4 weeks after their last dose of emapalumab.
  • Live-virus vaccination within 4 weeks of study entry or anticipated need for a live or live attenuated vaccine within 4 weeks after the last dose of emapalumab
  • Peceived Bacillus Calmette-Guerin vaccine within 12 weeks prior to screening
  • Patient or parent/guardian unable to give informed consent or unable to comply with the treatment protocol
  • Prisoners will be excluded

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Intervention Cohort

Participants on the Intervention Cohort will receive a combination of immunomodulatory regimen using emapalumab and methylprednisolone (or prednisone equivalent), aimed at controlling severe immune-mediated hepatitis and preventing progression to liver failure.

Participants will be monitored closely for clinical improvement, laboratory normalization, and adverse events throughout the 56-day treatment period, with continued follow-up through Day 180 to assess long-term outcomes, including relapse, liver failure, survival, and safety.

Participants on the Intervention Cohort will receive a combination of immunomodulatory regimen using emapalumab and methylprednisolone (or prednisone equivalent), aimed at controlling severe immune-mediated hepatitis and preventing progression to liver failure.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of Liver Failure
Zeitfenster: 30, 90, and 180 days after the start of emapalumab
INR >2 on two consecutive occasions without hepatic encephalopathy (HE), or INR ≥1.5 with evidence of HE
30, 90, and 180 days after the start of emapalumab

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Complete Response (CR)
Zeitfenster: throughout study participation/ up to 180 days
A complete response (CR) is defined by normalization or near-normalization of liver injury markers and hepatic function. Patients achieving CR will demonstrate an ALT < 2.5X ULN together with an INR ≤ 1.2.
throughout study participation/ up to 180 days
Cytokine and Chemokine Profiling
Zeitfenster: through study participation/ up to 180 days
The cytokine milieu including interferon-γ, interferon-stimulated gene products, TNF-α, IL-6, IL-18, CXCL9, and others will be quantified to define the inflammatory environment at baseline and during treatment.
through study participation/ up to 180 days
Emapalumab Immunologic Effects
Zeitfenster: through study completion/ up to 180 days
Change in circulating activated CD8+ T cells from the initiation of emapalumab to Days 7, 14, 30, 60, 90, and 180 of study
through study completion/ up to 180 days
Incidence and Severity of Adverse Events
Zeitfenster: from first emapalumab dose through study completion, up to 180 days
Incidence of all adverse events of all grades as defined by CTCAE version 5.0
from first emapalumab dose through study completion, up to 180 days
Population Summary Measure
Zeitfenster: throughout study participation/ up to 180 days
The population summary measure will be the Complete Response rate, which will be estimated as the number of participants with Complete Response divided by the total number of participants in the efficacy sample population.
throughout study participation/ up to 180 days
Time to First Complete Response
Zeitfenster: throughout study participation/ up to 180 days
Time to first CR will be estimated using time-to-event methods. Death or liver transplant before CR will be treated as competing risks, and cumulative incidence functions will be used to estimate probabilities.
throughout study participation/ up to 180 days
Partial Response (PR)
Zeitfenster: throughout study participation/ up to 180 days
This is defined as an ALT decrease 50% from initiation of emapalumab, but ALT >2.5X ULN with INR< 1.2.
throughout study participation/ up to 180 days
Sustained Response Off Therapy (SR)
Zeitfenster: throughout study participation/ up to 180 days
ALT levels remaining < 2.5X ULN for at least two consecutive months after completion of emapalumab.
throughout study participation/ up to 180 days
Non-Response (NR)
Zeitfenster: After 4 doses of emapalumab/ about 2 weeks after start of therapy
Patients are considered non-responders if clinically relevant worsening with progression to liver failure.
After 4 doses of emapalumab/ about 2 weeks after start of therapy
Proportion of Patients with Overall Response (CR or PR)
Zeitfenster: from first dose of emapalumab to week 8 of therapy
The proportion of patients achieving overall response (OR, defined as CR or PR) will be reported at Week 8 with exact confidence intervals. Missing values will be treated as non-response
from first dose of emapalumab to week 8 of therapy
Time to First Overall Response (OR)
Zeitfenster: throughout study participation/ up to 180 days
Time to first OR will be analyzed using cumulative incidence methods, with death or liver transplant treated as competing risks.
throughout study participation/ up to 180 days
Sustained CR Off Therapy at Day 180
Zeitfenster: 180 days on study therapy
The proportion of patients achieving a sustained CR off therapy (SROT) at Day 180 will be summarized with exact confidence intervals. Patients without Day 180 data or therapy information will be considered non-SROT.
180 days on study therapy
Overall Survival with Native Liver
Zeitfenster: days 30, 60, 90, and 180
Survival with native liver will be estimated using Kaplan-Meier methods. Survival probabilities and 95% confidence intervals will be presented at each landmark time point.
days 30, 60, 90, and 180
Proportion of Patients Receiving Liver Transplantation:
Zeitfenster: days 30, 90, and 180
Cumulative incidence of transplant will be calculated at Days 30, 90, and 180, with death as a competing risk.
days 30, 90, and 180
Change in Systemic Inflammatory Markers
Zeitfenster: throughout study participation/ up to 180 days
Longitudinal changes in sIL2R, and CXCL9 will be evaluated using mixed-effects models for repeated measures.
throughout study participation/ up to 180 days
Change in Circulating Activated CD8+ T Cells
Zeitfenster: throughout study participation/ up to 180 days
Changes in activated CD8+ T cells over time will be analyzed similarly with mixed-effects models, supplemented by graphical summaries.
throughout study participation/ up to 180 days
Corticosteroid Exposure and Time to Discontinuation
Zeitfenster: throughout study participation/ up to 180 days
Cumulative corticosteroid exposure (prednisone equivalents) will be summarized descriptively. Time to discontinuation will be estimated using Kaplan-Meier methods, with competing-risk analyses considering death or transplant.
throughout study participation/ up to 180 days
Incidence of Hepatitis Relapses
Zeitfenster: After initial improvement during weaning or cessation of therapy, up to Day 180
Defined as ALT re-elevation with concurrent sIL2R and CXCL9 rise. Time-to-relapse will be summarized with cumulative incidence functions.
After initial improvement during weaning or cessation of therapy, up to Day 180

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Mitarbeiter

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. September 2026

Primärer Abschluss (Geschätzt)

1. September 2031

Studienabschluss (Geschätzt)

1. September 2032

Studienanmeldedaten

Zuerst eingereicht

29. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

31. Juli 2026

Zuerst gepostet (Tatsächlich)

4. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

4. August 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

31. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • SHIELD (Jacobs Institute)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

Study participant research data, which is for purposes of statistical analysis and scientific reporting, will be stored. This will not include the participant's contact or identifying information. Rather, individual participants and their research data will be identified by a unique study identification number. The study data entry and study management systems used by clinical sites and research staff will be secured and password protected.

Neither data nor specimens will be shared across participating sites. Deidentified data that supports the findings of this study will be made available by the Principal Investigator, upon reasonable request.

At the end of the study, all records will continue to be kept in a secure location for as long a period as dictated by local IRB and Institutional regulations. All study databases will be de-identified and archived.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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