- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07763015
Study of Resmetirom in Children and Adolescents With MASH
10. September 2026 aktualisiert von: Madrigal Pharmaceuticals, Inc.
A Phase 2a, Multicenter, Open-label, Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Resmetirom in Pediatric Subjects Ages 6-17 Years With MASH With Fibrosis Stage F1-F3
This study will evaluate the safety, pharmacokinetics (how the body absorbs, distributes, metabolizes, and eliminates the drug), and pharmacodynamics (how the drug affects the body) of resmetirom in children and adolescents with metabolic dysfunction-associated steatohepatitis (MASH) and liver fibrosis.
Participants will receive oral resmetirom once daily for approximately 14 days at one of several dose levels.
The information from this study will help determine appropriate dosing and further evaluate the safety and biological effects of resmetirom in pediatric participants with MASH.
Studienübersicht
Status
Rekrutierung
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Geschätzt)
61
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
- Name: Tom Hare
- Telefonnummer: 267-406-0611
- E-Mail: info@madrigalpharma.com
Studienorte
-
-
Indiana
-
Indianapolis, Indiana, Vereinigte Staaten, 46402
- Rekrutierung
- Riley Hospital for Children at IU Health
-
-
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
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
Inclusion Criteria:
- Male or female participants 6 to 17 years of age, inclusive.
- Parent(s) or legal guardian(s) able to provide written informed consent (as required by local regulations), with participant assent obtained as applicable.
- Diagnose of MASH with fibrosis stage F1-F3 based on a liver biopsy obtained within 24 months before Screening.
- Hepatic fat fraction ≥8% by magnetic resonance imaging-proton density fat fraction (MRI-PDFF) obtained during the Screening period.
- Able to swallow study tablets.
- Females of childbearing potential must have a negative pregnancy test at screening, must not be pregnant or breastfeeding, and must agree to use a highly effective method of contraception during the study and for at least 30 days after the last dose of study drug. Premenarchal participants and those not of childbearing potential are eligible without contraception.
Exclusion Criteria:
- Previous exposure to resmetirom.
- Clinically significant liver disease other than MASH or evidence of cirrhosis (F4), decompensated liver disease, or other hepatic conditions that may interfere with study participation or interpretation of results.
- Clinically significant thyroid disease or use of thyroid replacement therapy, triiodothyronine, thyroxine, or other prohibited thyroid medications.
- Use of prohibited concomitant medications, including medications known to affect hepatic steatosis or liver function, lipid-lowering therapies, CYP2C8 inhibitors, OATP1B1/OATP1B3/BCRP inhibitors, protease inhibitors, St. John's Wort, or other medications prohibited by the protocol.
- Use of glucagon-like peptide-1 (GLP-1) receptor agonists unless on a stable dose for at least 24 weeks before screening.
- Clinically significant alcohol or substance abuse, or regular use of tobacco/nicotine products within 6 months before screening.
- Active or clinically significant infection, including chronic hepatitis B or hepatitis C infection, HIV infection, or other immunocompromising conditions.
- History or presence of clinically significant cardiovascular, pulmonary, renal, gastrointestinal, neurologic, hematologic, endocrine, psychiatric, or other medical conditions that, in the opinion of the Investigator, could interfere with study participation or interpretation of study results.
- History of malignancy within the past 5 years (except adequately treated non-melanoma skin cancer or other protocol-permitted exceptions).
- History of organ transplantation or known immunocompromised status.
- Participation in another investigational study within 60 days or 5 half-lives (whichever is longer) before screening, unless permitted by the protocol.
- Major surgery within 6 weeks before screening.
- Known hypersensitivity to resmetirom or any excipient.
- Females who are pregnant or breastfeeding.
- Any condition that, in the opinion of the Investigator, would compromise participant safety, compliance, or the integrity of the study.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Sequenzielle Zuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Adolescent Dose-Escalation Cohort 1
Adolescents participants 12 to 17 years of age receive the first planned dose level of oral resmetirom once daily for approximately 14 days
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Adolescent Dose-Escalation Cohort 2
Adolescent participants 12 to 17 years of age receive the second planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Adolescent Dose-Escalation Cohort 3
Adolescent participants 12 to 17 years of age receive the third planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Adolescent Dose-Escalation Cohort 4
Adolescent participants 12 to 17 years of age receive the fourth planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Adolescent Dose-Escalation Cohort 5
Adolescent participants 12 to 17 years of age receive the fifth planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Child Dose-Escalation Cohort 6
Children participants 6 to 11 years of age receive the first planned dose level of oral resmetirom once daily for approximately 14 days.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Child Dose-Escalation Cohort 7
Children participants 6 to 11 years of age receive the second planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Child Dose-Escalation Cohort 8
Children participants 6 to 11 years of age receive the third planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
|
Experimental: Child Dose-Escalation Cohort 9
Children participants 6 to 11 years of age receive the fourth planned dose level of oral resmetirom once daily for approximately 14 days following review of safety and PK data.
|
Resmetirom (MGL-3196) : Oral resmetirom administered once daily.
Participants receive one of several protocol-defined dose levels assigned according to the sequential multiple ascending-dose study design.
Dose escalation proceeds following review of available safety, pharmacokinetic, and pharmacodynamic data.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety and tolerability of multiple ascending doses of resmetirom
Zeitfenster: Baseline through approximately Day 21 (or the protocol-defined safety follow-up period)
|
Safety and tolerability will be assessed by the incidence and severity of adverse events, serious adverse events, clinical laboratory evaluations, vital signs, 12-lead electrocardiograms, physical examinations, and other protocol-defined safety assessments.
|
Baseline through approximately Day 21 (or the protocol-defined safety follow-up period)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Pharmacokinetic parameters of resmetirom (MGL-3196) and its metabolite (MGL-3623)
Zeitfenster: Day 1 through Day 14
|
Pharmacokinetic parameters of resmetirom and MGL-3623 following single and repeated dosing, including CL/F (parent only), Vz/F (parent only), Cmax, AUC0-24, and AUC0-∞ after the first dose, and CL/F (parent only), Cmax, and AUC0-24 following repeated dosing, as applicable.
|
Day 1 through Day 14
|
|
Pharmacodynamic biomarkers associated with resmetirom exposure
Zeitfenster: Baseline through Day 21
|
Changes in pharmacodynamic biomarkers, including thyroid axis markers, sex hormone-binding globulin, and lipid parameters and their relationship to dose and/or plasma concentrations of resmetirom.
|
Baseline through Day 21
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
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 (Tatsächlich)
1. August 2026
Primärer Abschluss (Geschätzt)
1. Juli 2029
Studienabschluss (Geschätzt)
1. Juli 2029
Studienanmeldedaten
Zuerst eingereicht
10. August 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
10. August 2026
Zuerst gepostet (Tatsächlich)
13. August 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
11. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
10. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- MGL-3196-29
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
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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