Nonalcoholic Fatty Liver Disease
Conditions
Keywords
Fatty Liver Disease, Liver Disease, Fatty Liver, Nonalcoholic Liver
Brief summary
This is a 3 part, randomized, double blind, placebo controlled study evaluating the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single and multiple ascending subcutaneous (SC) doses of CB4211 in healthy non obese subjects and subjects with NAFLD.
Detailed description
Part A: Part A is a randomized, double blind, placebo controlled, single ascending dose sequential group study evaluating the safety, tolerability, PK, and PD of a single SC dose of CB4211 in healthy non obese subjects. Part B: Part B is a randomized, double blind, placebo controlled, multiple ascending dose sequential group study evaluating the safety, tolerability, PK, and PD of once daily SC doses of CB4211 over 7 days in healthy non obese subjects. Part C: Part C is a randomized, double blind, placebo controlled, multiple dose, parallel group study evaluating the safety, tolerability, PK, and PD of once daily SC doses of CB4211 over 28 days in subjects with NAFLD.
Interventions
DRUGCB4211 Dose 1
Administered by subcutaneous injection
DRUGCB4211 Dose 2
Administered by subcutaneous injection
DRUGCB4211 Dose 3
Administered by subcutaneous injection
DRUGCB4211 Dose 4
Administered by subcutaneous injection
DRUGCB4211 Dose 5
Administered by subcutaneous injection
DRUGCB4211 Dose 6
Administered by subcutaneous injection
DRUGCB4211 Dose TBD
Administered by subcutaneous injection
DRUGPlacebo
Administered by subcutaneous injection
Sponsors
CohBar, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
randomized, double blind, placebo controlled
Intervention model description
This is a 3-part, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, PK, and PD of single- and multiple-ascending SC doses of CB4211 in healthy subjects and subjects with NAFLD. Study treatment (CB4211 or placebo) will be administered SC into the abdomen (and if needed, upper and lower thigh) as bolus injections.
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
Parts A and B Inclusion Criteria: 1. Males or females of nonchildbearing potential, of any race, 18 to 60 years of age, inclusive, at Screening. Females of nonchildbearing potential are defined as permanently sterile (ie, due to hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) confirmed by history or postmenopausal (defined as at least 12 continuous months without menses and follicle-stimulating hormone (FSH) ≥40 milli-International unit (mIU)/L and without an alternative medical cause). 2. Body mass index between 18.0 and 30.0 kg/m2 , inclusive, with a minimum body weight of 50.0 kg at Screening. 3. In good health, determined by no clinically significant findings from medical history, physical examination, 12-lead ECG, vital signs measurements, and clinical laboratory evaluations (congenital nonhemolytic hyperbilirubinemia \[eg, Gilbert's syndrome\] is not acceptable) at Screening or Check-in as assessed by the Investigator (or designee). 4. Males will agree to use contraception. 5. Has maintained stable weight (by history) for at least 4 weeks prior to Screening. 6. Agrees to the following: * Not to initiate a weight-loss program from Screening until the Follow-up visit; * To refrain from strenuous exercise from 7 days before Check-in until the Follow-up visit; * To maintain consistent dietary habits and exercise routines for the duration of the study. 7. Must have transaminases (aspartate aminotransferase (AST) and alanine aminotransferase (ALT)) and total bilirubin within the normal range at Screening and Check-in. For other laboratory evaluations, the subject may be included only if the Investigator judges the abnormalities or deviations from normal to be not clinically significant. 8. Able to comprehend and willing to sign an informed consent form (ICF) and to abide by the study restrictions. Parts A and B
Exclusion criteria
1. Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the Investigator (or designee). 2. Clinically significant ECG abnormalities or QT interval corrected for heart rate using Fridericia's method (QTcF) \>450 milliseconds for males and \>470 milliseconds for females at either Screening or Check-in, or any prior history of QT abnormality. 3. Creatinine clearance of \<90 mL/min at Screening, determined using the Cockcroft-Gault (C-G) equation. 4. History of febrile illness within 7 days prior to the first dose of study drug or subjects with evidence of active infection. 5. History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee). 6. History of alcoholism or drug/chemical abuse within 2 years prior to Check-in. 7. Alcohol consumption of \>21 units per week for males and \>14 units for females. One unit of alcohol equals 12 oz (360 mL) beer, 1½ oz (45 mL) liquor, or 5 oz (150 mL) wine. 8. Positive urine drug screen (confirmed by repeat) at Screening or positive alcohol breath or urine test result or positive urine drug screen at Check-in. 9. Positive hepatitis panel and/or positive human immunodeficiency virus test. Subjects with serologic finding of immunity consistent with history of prior hepatitis B vaccination may be enrolled. 10. Participation in a clinical study involving administration of an investigational drug (new chemical entity) in the past 30 days prior to dosing or have received a biological product within 3 months or 5 elimination half-lives (whichever is longer) prior to dosing. 11. Use of prescription drugs, nonprescription drugs, dietary supplements including Vitamin E, herbal supplements, hormonal therapy/replacement, or CYP3A4 substrates, inducers and inhibitors within 14 days prior to the first dose of study drug unless, in the opinion of the Investigator and Sponsor's Medical Monitor, the medication will not interfere with the study procedures or compromise subject safety. 12. Use or intend to use slow-release medications/products considered to still be active within 14 days prior to Check-in, unless deemed acceptable by the Investigator (or designee). 13. Use or intend to use any nonprescription medications/products including vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations within 14 days prior to the first dose of study medication, unless deemed acceptable by the Investigator (or designee). 14. Use of tobacco- or nicotine-containing products within 3 months prior to Check-in. 15. Receipt of blood products within 2 months prior to Check-in. 16. Donation of blood from 56 days prior to Screening, plasma from 2 weeks prior to Screening, or platelets from 6 weeks prior to Screening. 17. Poor peripheral venous access. 18. Have previously completed or withdrawn from this study or any other study investigating CB4211, and have previously received the investigational product. 19. Subjects who, in the opinion of the Investigator (or designee), should not participate in this study. Part C Inclusion Criteria: 1. Males or females of nonchildbearing potential, of any race, 18 to 60 years of age, inclusive, at Screening. Females of nonchildbearing potential are defined as permanently sterile (ie, due to hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) confirmed by history or postmenopausal (defined as at least 12 continuous months without menses and FSH ≥40 mIU/L and without an alternative medical cause). 2. Body mass index ≥30.0 kg/m2, and body weight ≤115 kg at Screening. 3. History of Fatty Liver Index (FLI) score \>60, FLI score \>60 at Screening, or documented history of fatty liver with imaging results (eg, standard positive ultrasound or Fibroscan controlled attenuation parameter (CAP) \>300 decibels (dB)/m) indicating liver fat \>10% within 6 months of Screening. A formal diagnosis of nonalcoholic fatty liver disease (NAFLD) is not required. 4. Liver fat content ≥10% as determined by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) within 14 days prior to Check in. One repeat Baseline MRI-PDFF will be allowed if the first value is below 10%, but greater than or equal to 9.5%. The repeat MRI must be within 14 days of the first MRI, and enrollment must be within 14 days of the repeat MRI. The most current MRI will serve as the baseline. (When available, Fibroscan indicating a CAP \>300 dB/m within 6 weeks prior to Check-in may be used as a pre-selection test prior to MRI being performed) 5. No history of common causes of secondary hepatic steatosis such as: 1. Macrovesicular steatosis: excessive alcohol consumption, hepatitis C (genotype 3), Wilson's disease, lipodystrophy, starvation, parenteral nutrition, abetalipoproteinemia, medications (eg, amiodarone, methotrexate, tamoxifen, corticosteroids, or any drug known to affect hepatic steatosis or insulin resistance) 2. Microvesicular steatosis: Reye's syndrome, medications (valproate, anti-retroviral medicines), acute fatty liver of pregnancy, HELLP syndrome, inborn errors of metabolism (eg, lecithin-cholesterol acyltransferase deficiency, cholesterol ester storage disease, Wolman disease, lysosomal acid lipase deficiency) 6. Glycosylated hemoglobin A1c \<7.0 % at Screening. 7. Fasting blood glucose of ≥100 to \<126 mg/dL at Screening. 8. Serum triglyceride level ≤500 mg/dL at Screening 9. Have international normalized ratio (INR) \< upper limit of normal (ULN) and platelet count \>150,000 at Screening and Check-in. For other abnormalities, the subject may be included only if the Investigator judges the abnormalities or deviations from normal to be not clinically significant. 10. In subjects with ALT, AST, alkaline phosphatase (ALP), or total bilirubin \> ULN at Screening, the baseline measurement (BLM) should be determined by 2 separate measurements obtained approximately 4 weeks apart. To be eligible for study entry, the Screening ALT, AST, ALP, and total bilirubin must be \< ULN or the following criteria must be met prior to randomization: 1. ALT ≤3 x ULN for both measurements and the difference between the measurements should be \<20% of the lower value; 2. AST ≤3 x ULN for both measurements and the difference between the measurements should be \<20% of the lowest value; 3. ALP ≤3 x ULN for both measurements and the difference between the measurements should be \<20% of the lowest value; 4. Total bilirubin ≤2 x ULN for both measurements and the difference between the measurements should be \<20% of the lowest value. 11. In good health, determined by no clinically significant findings from medical history, physical examination, 12-lead ECG, vital signs measurements, and clinical laboratory evaluations (congenital nonhemolytic hyperbilirubinemia \[eg, Gilbert's syndrome\] is not acceptable) at Screening or Check-in as assessed by the Investigator (or designee). 12. Males must agree to use contraception. 13. Has maintained stable weight (by history) for at least 4 weeks prior to Screening. 14. Agrees to maintain consistent dietary habits and exercise routines for the duration of the study, including avoiding : * initiating any weight-loss program from Screening until the Follow-up visit; * strenuous exercise from 7 days before Check-in until the Follow-up visit; 15. Able to comprehend and willing to sign an ICF and to abide by the study restrictions. Part C
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Physical examinations | Time Frame: up to 8 weeks for Part A; up to 9 weeks for Part B; up to 12 weeks for Part C | Number of participants with clinically significant abnormalities in physical examinations |
| Vital Signs | 7 days for Part A; 2 weeks for Part B; 5 weeks for Part C | Number of participants with clinically significant abnormalities in vital signs |
| Injection-site assessments | up to 8 weeks for Part A; up to 9 weeks for Part B; up to 12 weeks for Part C | Number of participants with treatment-related injection site reactions |
| Clinical laboratory evaluations | 7 days for Part A; 2 weeks for Part B; 5 weeks for Part C | Number of participants with clinically significant abnormalities in clinical laboratory values |
| 12-lead ECG parameters | 7 days for Part A; 2 weeks for Part B; 5 weeks for Part C | Number of participants with clinically significant abnormalities in 12-lead ECGs |
| Incidence and severity of adverse events (AEs) | up to 8 weeks for Part A; up to 9 weeks for Part B; up to 12 weeks for Part C | Number of participants with treatment-related adverse events and serious adverse events |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration (AUC0-t) |
| Area under the blood/plasma concentration time curve from time zero to 24 hours postdose of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Area under the blood/plasma concentration time curve from time zero to 24 hours postdose (AUC0-24) |
| Time of the maximum observed blood/plasma concentration of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Time of the maximum observed blood/plasma concentration (Tmax) |
| Apparent blood/plasma terminal elimination half life of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Apparent blood/plasma terminal elimination half life (t1/2) |
| Apparent total blood/plasma clearance of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Apparent total blood/plasma clearance (CL/F) |
| Apparent volume of distribution of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Apparent volume of distribution(Vz/F) |
| Maximum observed blood/plasma concentration of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Maximum observed blood/plasma concentration (Cmax) |
| Amount of CB4211 excreted in urine over the sampling interval | 24 hours for Part A, 7 days for Part B | Amount of CB4211 excreted in urine over the sampling interval (Aeu) |
| Percentage of CB4211 excreted in urine | 24 hours for Part A, 7 days for Part B | Percentage of CB4211 excreted in urine (%fe) |
| Renal clearance of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Renal clearance (CLr) |
| Incidence of antidrug antibodies (ADAs) | Sample at Day -1 and 5 to 7 days postdose for Part A, Day -1, Day 9 prior to discharge and 5 to 7 days post final dose for Part B, and Day -1, Days 14 and 28 predose, and 5 to 7 days post final dose for Part C | Number of participants with antidrug antibodies (ADAs) |
| Area under the blood/plasma concentration time curve from time zero to infinity of CB4211 | 24 hours for Part A, 7 days for Part B, 28 days for Part C | Area under the blood/plasma concentration time curve from time zero to infinity (AUC0-inf) |
Other
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in body weight | 28 days for Part C only | Change from baseline in body weight |
| Exploratory biomarkers | Samples pre dose and post dose at 4, 8, 12, and 24 hours for Part A, at 7 days for Part B, and at 7, 14, 21 and 28 days for Part C | For Parts A, B, and C, exploratory biomarker endpoints include glucose, insulin, triglycerides, non-esterified free fatty acids (NEFA), ALT, adiponectin, and other biomarkers may also be measured in an exploratory fashion. Changes from baseline at 24 hours (Part A), Day 7 (Part B) and Days 7, 14, 21, and 28 (Part C) will be assessed in glucose, insulin; triglycerides, NEFA, ALT, adiponectin, and other biomarkers as required. |
| Proportion of subjects achieving various levels of liver fat reduction at end of treatment | 28 days for Part C | Proportion of subjects achieving various levels of liver fat reduction at end of treatment |
| Change from baseline in liver fat (as determined by magnetic resonance imaging-derived proton density fat fraction [MRI-PDFF]) | 28 days for Part C only | Change from baseline in liver fat (as determined by magnetic resonance imaging-derived proton density fat fraction \[MRI-PDFF\]) |
Countries
United States
Outcome results
None listed