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Severe Hepatitis Intervention With Emapalumab for Liver Disease (SHIELD)

2026년 7월 31일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

상세 설명

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).

연구 유형

중재적

등록 (추정된)

28

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Incidence of Liver Failure
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Complete Response (CR)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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:
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 1일

기본 완료 (추정된)

2031년 9월 1일

연구 완료 (추정된)

2032년 9월 1일

연구 등록 날짜

최초 제출

2026년 5월 29일

QC 기준을 충족하는 최초 제출

2026년 7월 31일

처음 게시됨 (실제)

2026년 8월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 31일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

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.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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