- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07763015
Study of Resmetirom in Children and Adolescents With MASH
10 septembre 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Recrutement
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
61
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Tom Hare
- Numéro de téléphone: 267-406-0611
- E-mail: info@madrigalpharma.com
Lieux d'étude
-
-
Indiana
-
Indianapolis, Indiana, États-Unis, 46402
- Recrutement
- Riley Hospital for Children at IU Health
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
Non
La description
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.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
|
Expérimental: 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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Safety and tolerability of multiple ascending doses of resmetirom
Délai: 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)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Pharmacokinetic parameters of resmetirom (MGL-3196) and its metabolite (MGL-3623)
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 août 2026
Achèvement primaire (Estimé)
1 juillet 2029
Achèvement de l'étude (Estimé)
1 juillet 2029
Dates d'inscription aux études
Première soumission
10 août 2026
Première soumission répondant aux critères de contrôle qualité
10 août 2026
Première publication (Réel)
13 août 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
11 septembre 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
10 septembre 2026
Dernière vérification
1 septembre 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- MGL-3196-29
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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