- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07859813
A Trial to Evaluate the Efficacy and Safety of ARO-INHBE in Adults With Metabolic Dysfunction-Associated Steatohepatitis
A Phase 2, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of ARO-INHBE in Adults With Metabolic Dysfunction-Associated Steatohepatitis With or Without Type 2 Diabetes Mellitus
This study is designed to evaluate the safety and efficacy of ARO-INHBE in adults with suspected metabolic dysfunction-associated steatohepatitis (MASH).
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
- Navn: Medical Monitor
- Telefonnummer: 626-304-3400
- E-post: AROINHBE@arrowheadpharma.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Key Inclusion Criteria:
- BMI between 30.0 to 50.0 kilograms (kg)/square meter (m^2) (inclusive) with body weight ≤159 kg at Screening
- Stable body weight
- Participants on background glucagon-like peptide-1 (GLP-1) (or GLP-1/glucose-dependent insulinotropic polypeptide [GIP]) therapy must be on a stable dose for ≥6 months
- Participants not on GLP-1 (or GLP-1/GIP) therapy must be treatment naïve or off therapy for ≥6 months.
Key Exclusion Criteria:
- Clinical or laboratory signs of decompensated liver disease, history of esophageal varices, ascites, or hepatic encephalopathy, or history of cirrhosis on biopsy performed prior to Screening.
- History or evidence of hepatic disease of non-metabolic dysfunction-associated steatotic liver disease (MASLD) etiology (viral hepatitis, alcoholic liver disease, primary biliary cholangitis [PBC], primary sclerosing cholangitis [PSC], Wilson's disease, alpha-1 antitrypsin [A1AT] deficiency, hemochromatosis, or autoimmune hepatitis).
- Type 1 diabetes mellitus (T1DM) or uncontrolled Type 2 diabetes mellitus (T2DM).
- Use of non-GLP-1 receptor medications known to cause weight loss within 3 months prior to Screening.
- Use of medications associated with weight gain (for example, tricyclic antidepressants, mirtazapine, paroxetine, atypical antipsychotics) unless on a stable dose ≥3 months prior to Screening with anticipated continuation on this dose throughout the trial.
- Clinically significant end-organ disease.
- Major surgery within 90 days of Screening.
- Use of hepatocyte-targeted ribonucleic acid interference (RNAi) therapies within 6 months of Screening.
- Insulin use within 6 months of Screening (except short-term peri-procedural/inpatient use).
Note: Other protocol-defined Inclusion/Exclusion criteria may apply.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: ARO-INHBE Low Dose
Participants will receive ARO-INHBE at a low dose on Days 1, 85, 169, and 253. |
Subcutaneous (SC) injection |
|
Placebo komparator: Placebo for ARO-INHBE Low Dose
Participants will receive placebo on Days 1, 85, 169, and 253. |
SC injection |
|
Eksperimentell: ARO-INHBE High Dose (Schedule 1)
Participants will receive ARO-INHBE at a high dose on Days 1, 85, 169, and 253. |
Subcutaneous (SC) injection |
|
Placebo komparator: Placebo for ARO-INHBE High Dose (Schedule 1)
Participants will receive placebo on Days 1, 85, 169, and 253. |
SC injection |
|
Eksperimentell: ARO-INHBE High Dose (Schedule 2)
Participants will receive ARO-INHBE at a high dose on Days 1, 85, and 169. |
Subcutaneous (SC) injection |
|
Eksperimentell: Placebo for ARO-INHBE High Dose (Schedule 2)
Participants will receive placebo on Days 1, 85, and 169. |
SC injection |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percent Change From Baseline in Liver Fat Content (LFC) by Magnetic Resonance Imaging-proton Density Fat Fraction (MRI-PDFF) at Week 48
Tidsramme: Baseline, Week 48
|
Baseline, Week 48
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percentage of Participants With Resolution of Steatohepatitis and No Worsening of Liver Fibrosis (Histology)
Tidsramme: Week 48
|
Week 48
|
|
Percentage of Participants With Improvement in Liver Fibrosis by ≥1 Stage and No Worsening of Steatohepatitis (Histology)
Tidsramme: Week 48
|
Week 48
|
|
Change From Baseline in Non-alcoholic Fatty Liver Disease Activity Score (NAS) Total Score and Individual Subscores (Steatosis, Hepatocyte Ballooning, and Lobular Inflammation) at Week 48
Tidsramme: Baseline, Week 48
|
Baseline, Week 48
|
|
Change From Baseline in Fibrosis Stage (Histology) at Week 48
Tidsramme: Baseline, Week 48
|
Baseline, Week 48
|
|
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
Tidsramme: Baseline up to Week 48
|
Baseline up to Week 48
|
|
Change From Baseline in LFC by MRI-PDFF at Week 24
Tidsramme: Baseline, Week 24
|
Baseline, Week 24
|
|
Percentage of Participants With >30%, >50%, and >70% Reduction in LFC From Baseline by MRI-PDFF at Week 24 and Week 48
Tidsramme: Week 24 and Week 48
|
Week 24 and Week 48
|
|
Change From Baseline Through Week 48 in Body Weight
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
|
Change From Baseline Through Week 48 in Body Composition (Total Adipose Tissue [TAT], Visceral Adipose Tissue [VAT] Volume, and Total Lean Tissue [TLT]), by Whole-body Magnetic Resonance Imaging (WB-MRI)
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
|
Change From Baseline Through Week 48 in Serum Activin E Protein
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
|
Change From Baseline in Markers of Hepatic Steatosis at Week 48
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
|
Change From Baseline in Markers of Inflammation at Week 48
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
|
Change From Baseline in Markers of Fibrosis at Week 48
Tidsramme: Baseline through Week 48
|
Baseline through Week 48
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- AROINHBE-2001
Plan for individuelle deltakerdata (IPD)
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