This Phase 1/2 study will evaluate safety, efficacy, PK, and PD of FT-4101 as a single agent in overweight/obese subjects with NASH. The study may be conducted in up to 2 dosing cohorts.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
14
FT-4101 will be supplied as active capsules and will be administered per the protocol defined frequency and dose level.
FT-4101 placebo will be supplied as placebo capsule matching in size and color to all the active capsules and will be administered per the protocol defined frequency and dose level.
Deuterated water will be provided as individual ready-to-use, single dose bottles each containing 50 mL of deuterated water (70%).
ProSciento, Inc.
Chula Vista, California, United States
Catalina Research Institute
Montclair, California, United States
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
TEAEs were defined as an adverse events (AEs) with an onset that occurred after receiving the first dose of the study drug (AE start date greater than or equal to \[\>=\] first dose date) and within 30 days after receiving the last dose of the study drug (AE start date - last dose date less than or equal to \[\<=\] 30). Number of participants with TEAEs are reported.
Time frame: From start of study drug administration up to 20 weeks
Number of Participants With Clinically Significant Changes in Laboratory Values
Number of participants with clinically significant changes in laboratory values (hematology, serum chemistry, and urinalysis) are reported.
Time frame: Up to 20 weeks
Number of Participants With Clinically Significant Changes in Physical Examination
Number of participants with clinically significant changes in physical examination are reported.
Time frame: Up to 20 weeks
Change From Baseline in Vital Signs: Blood Pressure (BP)
Change from baseline in blood pressure (systolic and diastolic) are reported.
Time frame: Baseline, Day 92
Change From Baseline in Vital Signs: Heart Rate (HR)
Change from baseline in heart rate is reported.
Time frame: Baseline, Day 92
Change From Baseline in Vital Signs: Respiratory Rate
Change from baseline in respiratory rate is reported.
Time frame: Baseline, Day 92
Change From Baseline in Vital Signs: Temperature
Change from baseline in temperature is reported.
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Time frame: Baseline, Day 92
Change From Baseline in 12-lead Electrocardiogram (ECG) Parameters: ECG Mean Heart Rate
Change from baseline in ECG mean heart rate is reported.
Time frame: Baseline, Day 92
Change From Baseline in 12-lead ECG Parameters: QT Interval
Change from baseline in QT interval is reported.
Time frame: Baseline, Day 92
Change From Baseline in 12-lead ECG Parameters: PR Interval
Change from baseline in PR interval is reported.
Time frame: Baseline, Day 92
Change From Baseline in 12-lead ECG Parameters: QRS Interval
Change from baseline in QRS interval is reported.
Time frame: Baseline, Day 92
Change From Baseline in 12-lead ECG Parameters: RR Interval
Change from baseline in RR interval is reported.
Time frame: Baseline, Day 92
Change From Baseline in 12-lead ECG Parameters: QTc (Corrected) Using the Fridericia Correction (QTcF) Interval
Change from baseline in QTcF interval is reported.
Time frame: Baseline, Day 92
Percent Change From Baseline in Liver Fat on Magnetic Resonance Imaging- Proton Density Fat Fraction (MRI-PDFF)
Percent change from baseline in liver fat on MRI-PDFF is reported.
Time frame: At week 12
Change From Baseline in Liver Fat on Magnetic Resonance Imaging- Proton Density Fat Fraction (MRI-PDFF)
Change from baseline in percentage of liver fat on MRI-PDFF is reported.
Time frame: At week 12
Change From Baseline in Liver Fat on MRI-PDFF
Change from baseline in percentage of liver fat on MRI-PDFF is reported.
Time frame: At week 6
Percent Change From Baseline in Liver Fat on MRI-PDFF
Percent change from baseline in liver fat on MRI-PDFF is reported.
Time frame: At week 6
Percentage of Participants Experiencing a Relative Reduction of 30% or Greater of Liver Fat as Assessed by MRI-PDFF
Percentage of participants experiencing a relative reduction of 30% or greater of liver fat as assessed by MRI-PDFF at week 12 are reported.
Time frame: At week 12
Change From Baseline in Alanine Aminotransferase (ALT)
Change from baseline in ALT is reported.
Time frame: Baseline, Day 92
Change From Baseline in Aspartate Aminotransferase (AST)
Change from baseline in AST is reported.
Time frame: Baseline, Day 92
Change From Baseline in Gamma-glutamyl Transferase (γGT)
Change from baseline in γGT is reported.
Time frame: Baseline, Day 92
Change From Baseline in Alkaline Phosphatase
Change from baseline in alkaline phosphatase is reported.
Time frame: Baseline, Day 92
Change From Baseline in Total Bilirubin
Change from baseline in total bilirubin is reported.
Time frame: Baseline, Day 92
Maximum Plasma Concentration (Cmax) of FT-4101
Maximum plasma concentration (Cmax) of FT-4101 is reported
Time frame: Cycle 1 (Day 1), Cycle 4 (Day 14); each Cycle length = 21 days
Area Under the Concentration-time Curve for a Dosing Interval (AUCtau) of FT-4101
Time frame: Cycle 1 (Day 1), Cycle 4 (Day 14); each Cycle length = 21 days
Data for This Endpoint Was Not Collected and Analysed.
Time frame: Cycle 1 (Day 1), Cycle 4 (Day 14); each Cycle length = 21 days