A Study to Assess Safety, Tolerability, PK and PD of AZD2693 in Non-alcoholic Steatohepatitis Patients

AstraZeneca74 enrolled

Overview

This study is intended to investigate the safety and tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of AZD2693, following subcutaneous (SC) administration of multiple ascending doses in participants with Non-alcoholic Steatohepatitis (NASH) with fibrosis Stage 0 to 3 and who are carriers of the patatin-like phospholipase domain-containing 3 (PNPLA3) 148M risk alleles.

This study is a double blind, randomised, placebo-controlled, multi-centre study in participants with NASH and fibrosis stage between F0 (no fibrosis) and F3 (bridging fibrosis), and who are carriers of the PNPLA3 148M risk alleles. The study will comprise of: * An optional Pre-Screening Visit may be completed to determine PNPLA3 genotype and collect minimal baseline data and participants who are carriers of the PNPLA3 148M risk allele(s) will continue the study and enter the Screening Period. * A Screening Period with a maximum of 60 days. * For participants in all Cohorts, the dosing period will be 8 weeks during which participants will be resident of the study site for Dose 1 and Dose 3. Dose 1 will have participants reside at the study site from the day prior to study intervention administration (Day -1) until at least 2 days after study intervention administration with discharge on Day 3. Dose 2 will be administered at the study site on Day 29 with no overnight stay. Dose 3 will have participants reside at the study site from the day prior to study intervention administration (Day 56) until at least 2 days after study intervention administration with discharge on Day 59. * Each participant will be followed for approximately 15 weeks post last dose. The study will be performed at up to 30 study sites in the United States (US) and up to 5 study sites in Mexico. Approximately 80 participants comprising of male and female participants of non-childbearing potential may be enrolled into the first 4 cohorts of this study in order to achieve a target of 56 to 64 evaluable participants.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Non-alcoholic Steatohepatitis (NASH)

Interventions

AZD2693DRUG

Subcutaneous administration of AZD2693 multiple ascending doses in participants with NASH and who are carriers of the PNPLA3 148M risk allele(s).

PlaceboOTHER

Participants randomised to placebo will receive the corresponding dose volume of solution as participants receiving AZD2693 within the same cohort

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: For Cohorts 1 to 3: * An MRI-PDFF ≥7% and one of the following: * Previous liver biopsy: Acceptable if taken in the previous 3 years for fibrosis stages F0 to F2, or within the previous 1 year for stage F3; or * Previous imaging results taken in the previous 2 years: An MRE between 2.55 kPa and 3.63 kPa, or a vibration-controlled transient elastography (VCTE) between 7.1 kPa and 11.9 kPa; * Participants who are homozygous for rs738409 (PNPLA3 148M). Cohort 2 will enroll participants who are heterozygous for PNPLA3 148M. For Cohort 4: • An MRI-PDFF ≥ 7% and participant's consent for a liver biopsy. * Participants with suspected or confirmed Non-alcoholic fatty liver disease (NAFLD) or NASH are eligible for the Screening liver biopsy if they meet main protocol inclusion/exclusion criteria AND have any of the following: Alanine aminotransferase \> Upper Limit of Normal (ULN) but \< 3 × ULN, OR Imaging demonstrating hepatic steatosis including attenuation parameter (CAP) \> 290dB/m, OR A Magnetic resonance elastography (MRE) between 2.55 kPa and 3.63 kPa, or a vibration-controlled transient elastography (VCTE) between 7.1 kPa and 11.9 kPa. * Histologic evidence of NAFLD or NASH with a NASH Activity Score (NAS) ≥ 3 (independent of subcategory scoring) following Screening liver biopsy. * Participants who are homozygous for rs738409 (PNPLA3 148M). Exclusion Criteria: * History of liver transplant, or current placement on a liver transplant list (this may be checked at the optional Pre-Screening Visit). * History or presence of hepatic disease (with the exception of hepatic steatosis, NASH) or evidence of other known forms of known chronic liver disease such as alcoholic liver disease, hepatitis B, primary biliary cirrhosis, primary sclerotic cirrhosis, autoimmune hepatitis, Wilson disease, iron overload, alpha-1-antitrypsin deficiency, drug-induced liver injury, known or suspected hepatocellular carcinoma (this may be checked at the optional Pre-Screening Visit). * Histological or imaging (MRE or VCTE) evidence of cirrhosis. * Participants with history or pre-existing renal disease, as defined below: \- estimated glomerular filtration rate \< 60 mL/min/1.73 m\^2 (calculated using the Chronic Kidney Disease Epidemiology Collaboration formula) * Blood dyscrasias with increased risk of bleeding including idiopathic thrombocytopenic purpura and thrombotic thrombocytopenic purpura or symptoms of increased risk of bleeding (frequent bleeding gums or nose bleeds). * History of major bleed or high-risk of bleeding diathesis.

Locations (16)

Research Site

Chula Vista, California, United States

Research Site

La Mesa, California, United States

Research Site

Montclair, California, United States

Outcomes

Primary Outcomes

Number of participants with adverse events

Time frame: Up to 32 weeks (From Screening to Final Visit)

Secondary Outcomes

Absolute change from baseline to Week 8 and Week 12 in liver fat content (LFC)

Time frame: Baseline (Day 1), Week 8, Week 12

Percent change from baseline to Week 8 and Week 12 in liver fat content (LFC)

Time frame: Baseline (Day 1), Week 8, Week 12

Absolute change from baseline in Alanine Aminotransferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Percent change from baseline in Alanine Aminotransferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Absolute change from baseline in Aspartate Aminotransferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Percent change from baseline in Aspartate Aminotransferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Absolute change from baseline in Gamma Glutamyl Transferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Percent change from baseline in Gamma Glutamyl Transferase

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Absolute change from baseline in Enhanced Liver Fibrosis (ELF) score

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Data from ClinicalTrials.gov

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Research Site

San Diego, California, United States

Research Site

Doral, Florida, United States

Research Site

Hialeah, Florida, United States

Research Site

Hialeah, Florida, United States

Research Site

Miami Lakes, Florida, United States

Research Site

Indianapolis, Indiana, United States

Research Site

Morehead City, North Carolina, United States

...and 6 more locations

Percent change from baseline in ELF score

Time frame: Up to 32 weeks (From Pre-Screening to Final Visit)

Absolute change from baseline in plasma pharmacodynamic biomarker

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Percent change from baseline in plasma pharmacodynamic biomarker

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Absolute change from baseline in disease-specific biomarkers

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Percentage change from baseline in disease-specific biomarkers

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Absolute change from baseline β-Hydroxybutyrate and lipid profile

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Percent change from baseline β-Hydroxybutyrate and lipid profile

Time frame: Days 1, 8, 29, 36, 50, 64, and 78

Maximum observed plasma drug concentration (Cmax)

Time frame: Day 1 to Day 162

Time to reach maximum observed plasma concentration (tmax)

Time frame: Day 1 to Day 162

Terminal elimination rate constant, estimated by log-linear least-squares regression of the terminal part of the concentration-time curve (λz)

Time frame: Day 1 to Day 162

Apparent terminal elimination half-life associated with the terminal slope (λz) of the semi-logarithmic concentration-time curve, estimated as (ln2)/λz (t½λz)

Time frame: Day 1 to Day 162

Area under the plasma concentration-time curve from time zero to 48 hours after dosing (AUC(0-48h))

Time frame: Day 1 to Day 162

Area under the plasma concentration-curve from time zero to the time of last quantifiable analyte concentration (AUClast)

Time frame: Day 1 to Day 162

Area under the concentration-time curve from time zero extrapolated to infinity. AUC is estimated by AUClast + Clast/λz where Clast is the last observed quantifiable concentration (AUC)

Time frame: Day 1 to Day 162

Apparent total body clearance of drug from plasma after extravascular administration calculated as Dose/AUC (CL/F)

Time frame: Day 1 to Day 162

Mean residence time (MRT)

Time frame: Day 1 to Day 162

Time delay between drug administration and the first observed concentration in plasma (tlag)

Time frame: Day 1 to Day 162

Apparent volume of distribution for parent drug at terminal phase (extravascular administration), estimated by dividing the apparent clearance (CL/F) by λz (Vz/F)

Time frame: Day 1 to Day 162

Area under the plasma concentration-time curve from time zero to time of last quantifiable analyte concentration divided by the dose administered (AUClast/D)

Time frame: Day 1 to Day 162

Area under the plasma concentration-time curve from time zero extrapolated to infinity divided by the dose administered (AUC/D)

Time frame: Day 1 to Day 162

Observed maximum plasma concentration divided by the dose administered (Cmax/D)

Time frame: Day 1 to Day 162

Time of the last quantifiable concentration (tlast)

Time frame: Day 1 to Day 162

Maximum observed plasma drug concentration at steady state (Cssmax)

Time frame: Day 1 to Day 162

Minimum observed drug concentration at steady state (Cssmin)

Time frame: Day 1 to Day 162

Time to reach maximum observed plasma concentration at steady state (tssmax)

Time frame: Day 1 to Day 162

Area under the concentration-time curve in the dose interval (AUCss)

Time frame: Day 1 to Day 162

Apparent total body clearance of drug from plasma after extravascular administration calculated as Dose/AUCss (CLss/F)

Time frame: Day 1 to Day 162

Area under the plasma concentration-time curve from time zero extrapolated to infinity divided by the dose administered (AUCss/D)

Time frame: Day 1 to Day 162

Observed maximum plasma concentration divided by the dose administered (Cssmax/D)

Time frame: Day 1 to Day 162

Accumulation ratio based on Cmax (RacCmax)

Time frame: Day 1 to Day 162

Accumulation ratio based on AUC (RacAUC)

Time frame: Day 1 to Day 162

Temporal change parameter in systemic exposure (TCP)

Time frame: Day 1 to Day 162

Amount of analyte excreted into the urine from time t1 to t2 (Ae(t1-t2))

Time frame: Day 1 and Day 57: Pre-dose and between 0-6 hours, 6-12 hours, 12-24 hours, 24-36 hours and 36-48 hours post-dose

Cumulative amount of analyte excreted from time zero through the last sampling interval (Ae(0-last))

Time frame: Day 1 and Day 57: Pre-dose and between 0-6 hours, 6-12 hours, 12-24 hours, 24-36 hours and 36-48 hours post-dose

Fraction of dose excreted unchanged into the urine from time t1 to t2 (fe(t1-t2))

Time frame: Day 1 and Day 57: Pre-dose and between 0-6 hours, 6-12 hours, 12-24 hours, 24-36 hours and 36-48 hours post-dose

Cumulative fraction (%) of dose excreted unchanged into the urine from time zero to the last measured time point (fe(0-last))

Time frame: Day 1 and Day 57: Pre-dose and between 0-6 hours, 6-12 hours, 12-24 hours, 24-36 hours and 36-48 hours post-dose

Renal clearance of drug from plasma, estimated by dividing Ae(0-t) by AUC(0-t) where the 0-t interval is the same for both Ae and AUC (CLR)

Time frame: Day 1 and Day 57: Pre-dose and between 0-6 hours, 6-12 hours, 12-24 hours, 24-36 hours and 36-48 hours post-dose

Change from placebo to Week 10 in PNPLA3 messenger ribonucleic acid (mRNA) and protein expression (Cohort 4 only)

Time frame: Week 10

Change from baseline to Week 10 in PNPLA3 mRNA and protein expression (Cohort 4 only)

Time frame: Baseline, Week 10