TReatment for ImmUne Mediated PathopHysiology
Eligible age
1–18 yrs
Accepts
All genders
Locations
16 states
Healthy volunteers
No
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About this study
TReatment for ImmUne Mediated PathopHysiology (TRIUMPH) is a multi-center, three arm, randomized, controlled trial of immunosuppressive therapy for children with acute liver failure. The study will determine if suppressing inflammatory responses with either corticosteroids or equine anti-thymocyte globulin therapy improves survival for children with this rare, life-threatening condition.
Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
You may qualify if…
- ✓ 1. Patient with liver injury of ≤ 6 weeks duration resulting in an international normalization ratio (INR) of ≥ 1.5 or \< 2.0 (not corrected by vitamin K) with evidence of hepatic encephalopathy (HE), INR of ≥ 1.5 or \< 2.0 for at least 7 days duration without evidence of HE or INR ≥ 2.0 without evidence of HE.
- ✓ 2. Age is greater than or equal to 1 year and less than 18 years of age.
- ✓ 3. Patient or their legally authorized representative(s) (LAR) must consent (and assent, if applicable) to be in the study and must have signed and dated an approved informed consent form which conforms to federal and institutional guidelines.
- ✓ 4. Females of reproductive potential should not plan on conceiving children during the study and must agree to use a medically accepted form of contraception.
You may not qualify if…
- ✕ 1. Evidence of active infection with Hepatitis A, B, C, E or evidence of acute herpes simplex virus (HSV) or adenovirus infection
- ✕ 2. Travel within the past 3 months to an area highly endemic for Hepatitis E
- ✕ 3. Diagnosis of hemophagocytic lymphohistiocytosis (HLH) Note: Patients with a history of consanguinity and/or central nervous system (CNS) dysfunction that is exaggerated compared to the degree of liver dysfunction (as judged by the site investigator) will not be enrolled until results of rapid genetic testing are available. Turn-around time for genetic testing results is estimated to be 72-96 hours.
- ✕ 4. Aplastic anemia as defined by standardized criteria \[1\] diagnosed prior to enrollment
- ✕ 5. Diagnosis of autoimmune Hepatitis (AIH)
- ✕ 6. Diagnosis of acute Wilson disease
- ✕ 7. Diagnosis of inborn error of metabolism Note: Suspicion of metabolic disease is not an exclusion for entry into the Trial.
- ✕ 8. Diagnosis of acute drug or toxin-induced liver injury
Where it's recruiting
Los Angeles · Palo Alto · San Diego · San Francisco
Aurora
New Haven
Atlanta
Chicago
Indianapolis
Boston
Kansas City · St Louis
New York
Durham
Cincinnati · Cleveland
Philadelphia · Pittsburgh
Source: ClinicalTrials.gov · NCT04862221 · last updated 2026-05-14