Hepatic Impairment, Cholestatic Liver Disease, & NASH With Advanced Fibrosis & Normal Hepatic Function

Hepatic Impairment Clinical Trial

Official title:

Evaluation of Pharmacokinetics and Safety of Saroglitazar Magnesium in Participants With Normal Hepatic Function and With Hepatic Impairment, Cholestatic Liver Disease, NASH With Advanced Fibrosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04469920
• Other study ID #: SARO.19.003
• Status: Recruiting
• Phase: Phase 1
• Start date: July 16, 2020
• Est. completion date: October 2024

Study information

• Verified date: October 2023
• Source: Zydus Therapeutics Inc.
• Contact: Farheen A. Shaikh
• Phone: +1 6094534751
• Email: fshaikh[@]zydustherapeutics.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This will be a Phase 1, Open-label Study of Participants with Hepatic Impairment, Cholestatic Liver Disease, and NASH with Advanced Fibrosis and Normal Hepatic Function

Description:

Male and female participants 18-80 years of age (inclusive) with normal hepatic function or hepatic impairment/disease who meet all of the inclusion and none of the exclusion criteria. Subjects with hepatic impairment will be enrolled based upon the Child-Pugh-Turcotte (CPT) classification system for mild hepatic impairment (Group 1 CPT Class A without PHT; Group 2 CPT Class A with PHT), moderate hepatic impairment (Group 3 Decompensated CPT Class B), or severe hepatic impairment (Group 4 Decompensated CPT Class C). Group 5 will include subjects with cholestatic liver disease and Group 6 will include subjects with non-cirrhotic advanced fibrosis secondary to NASH (non-alcoholic steatohepatitis). The control group (Group 7) will consist of demographic matched subjects with normal hepatic function.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: October 2024
• Est. primary completion date: March 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Ability to comprehend and willingness to sign a written informed consent for the study.

2. Male or female aged 18 to 80 years (inclusive) at the time of signing the ICF.

3. Body mass index within the range 18.0 to 48.0 kg/m2 (inclusive) at screening.

4. Females must be non-pregnant, non-lactating and of non-childbearing potential or using highly efficient contraception for the full duration of the study.

5. Females of child-bearing potential and Males must agree to use contraception for the full duration of the study.

6. Ability to swallow and retain oral medication.

7. Groups 1 through 6 subjects may have medical findings consistent with their degree of hepatic dysfunction, as determined by medical history, physical examination, vital signs, ECGs, and clinical laboratory examinations at screening and check-in. Participants with abnormal findings considered not clinically significant by the Investigator are eligible.

8. Participants with hepatic impairment in Groups 1-4 will be classified at screening based on CPT score. If the hepatic impairment classification for the subject is not the same at screening and day -1, enrolment of the subject into a hepatic category group will be at the discretion of the hepatology Investigator.

9. Laboratory test values for Groups 1-4 hepatic impairment subjects must be clinically acceptable to the Investigator and meet all of the following parameters at Screening:

1. ALT/AST value = 10 × upper limit of normal (ULN)

2. Absolute neutrophil count (ANC) = 750/mm3

3. Platelets = 25,000/mm3

4. Hemoglobin = 8 g/dL

5. a-fetoprotein < 50 ng/mL or 50-80 ng/mL with concurrent negative imaging study (US, CT, MRI)

10. Group 2 must have evidence of PHT as manifested by one of the following:

1. presence of hepatic encephalopathy or ascites (on exam or imaging or medication to control these symptoms),

2. historical or current presence of varices by imaging or endoscopy,

3. historical or current presence of splenomegaly by imaging or physical exam,

4. previous Hepatic Venous Pressure Gradient Measurement (HVPG) >10 mmHg,

5. platelet count <150,000/mm3 (or /uL), or

6. Fibroscan® at screening >20 kPa.

11. Documented history of cholestatic liver disease (i.e. primary biliary cholangitis, primary sclerosing cholangitis) OR alkaline phosphatase at screening of >1.25 x ULN with AST/ALT <1.2 x ULN OR Historical presence of AMA (anti-mitochondrial antibody) >1:40 and elevated alkaline phosphatase > ULN at screening

12. Clinical diagnosis of NASH and the following criteria:

a. Screening Fibroscan® with liver stiffness > 8.5 kPa AND CAP >280 dB AND At least two criteria for metabolic syndrome modified from the NCEP

ATP III Guidelines, at screening:

i. Fasting glucose >100 mg/dL or receiving drug treatment for elevated glucose, ii. Fasting HDL cholesterol <40 mg/dL in men and <50 mg/dL in women or receiving drug treatment for low HDL cholesterol, iii. Fasting triglycerides > 150 mg/dL or receiving drug treatment for hypertriglyceridemia, iv. Waist circumference >102 cm for men or >88 cm for women or BMI >30 kg/m2, v. Systolic blood pressure >130 mmHg or diastolic blood pressure >85 mmHg or receiving drug treatment for hypertension

OR:

b. A historical liver biopsy within 6 months of screening consistent with NASH with stage 3 fibrosis and no documented weight loss >10% since date of liver biopsy

13. Subjects with normal hepatic function must match in age (± 10 years), gender, and weight (± 10 kg) with hepatic disease participants in the Groups 1-6.

14. Subjects should be in good health as determined by no clinically significant findings in the medical history, physical examination, vital signs, 12-lead electrocardiograms (ECGs), or laboratory examinations at Screening or Check-in.

15. Laboratory test values within normal limits or considered not clinically significant by the Investigator for subjects with normal hepatic function including ALT/AST < 1.2 × ULN at screening.

Exclusion Criteria:

1. Any significant, unstable medical condition or other instability that would prevent the subject from participating in the study as determined by the Investigator or designee.

2. History of malignancy of any type in the last 3 years of screening, with the exception of the following: in situ cervical or breast cancer or surgically excised non-melanoma skin cancers (i.e. basal cell or squamous cell carcinoma).

3. History of stomach or intestinal surgery or resection within the six months prior to screening that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy, cholecystectomy, and hernia repair will be allowed).

4. History of any significant drug allergy (such as anaphylaxis) deemed clinically relevant by the Investigator.

5. Any major surgery within 3 months of screening.

6. Donation of blood or blood products within 3 months prior to screening.

7. Current active infectious disease requiring systemic antibiotic, antifungal, or antiviral treatment or symptoms of active infectious disease within the two weeks prior to screening.

8. Use or intend to use any medications/products known to alter drug absorption, metabolism, or elimination processes, including St. John's Wort, within 21 days prior to screening, unless deemed acceptable by the Investigator.

9. Receiving or has received any investigational drug within the 30 days or 5 halflives (whichever is longer), before receiving Saroglitazar Magnesium.

10. Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2 by modification of diet in renal disease (MDRD) formula at screening.

11. Positive alcohol breath test at the time of check-in or those subjects who have current alcohol or substance abuse judged by the Investigator to potentially interfere with subject compliance or subject safety.

12. Positive test for drugs of abuse at screening or admission.

13. Any subject with poor peripheral venous access

14. Receipt of blood products within 1 month prior to check in.

15. Human immunodeficiency virus (HIV) type 1 antibody positive at screening for all groups.

16. Subjects who have had a change in hepatic disease status within 30 days of screening, as documented by the participant's medical history and deemed clinically significant by the Investigator.

17. Electrocardiogram QTcF > 500 msec, confirmed by repeat measurement OR presence of second- or third-degree atrioventricular (AV) block.

18. Subjects having -

1. History of gastrointestinal bleeding within 1 month prior to screening.

2. Current functioning organ transplant.

3. Evidence of severe ascites requiring frequent paracentesis in the opinion of investigator.

19. Subjects having a history of any of the following: hepatic encephalopathy, ascites, history or current presence of varices by imaging or endoscopy, history or current presence of splenomegaly by imaging or physical exam, previous HVPG >10, platelet count <150,000 (or /uL) at screening, or Fibroscan® at screening >20 kPa.

20. QT interval corrected for heart rate using Fridericia's method (QTcF) > 450 msec, confirmed by repeat measurement OR presence of second- or third-degree AV block.

21. Hepatitis B virus surface antigen (HBsAg) positive, Hepatitis C virus antibody (HCV-Ab) positive.

22. Subjects who use or intend to use any over the counter (vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations) or prescription medications within 30 days or 5 half-lives (whichever is longer) prior to enrolment, with the exception of hormone replacement therapy and therapies for hepatic disease and treatments of associated disorders that have been stable for at least 30 days prior to screening and until Day 1, unless deemed acceptable by the Investigator (or designee).

23. Other known cause of liver disease such as NASH, Alcoholic Steatohepatitis (ASH), autoimmune hepatitis, or acute or chronic viral hepatitis as determined by the Investigator and subject's medical records

24. Evidence of liver decompensation such as ascites, hepatic encephalopathy or prior history of variceal bleed.

25. No other known cause of liver disease such as Primary Biliary Cholangitis (PBC), Primary Sclerosing Cholangitis (PSC), Alcoholic Steatohepatitis (ASH), autoimmune hepatitis, or acute or chronic viral hepatitis as determined by the Investigator and subject's medical records

26. Platelet count <150,000 (or /uL)

27. Subjects who have taken any prescription medications or over-the-counter medications, including herbal products, within 14 days prior to start of study drug dosing, with the exception of vitamins, acetaminophen, hormonal contraceptive medications and/or any other over-the-counter product approved by the Investigator.

Related Conditions & MeSH terms

• Hepatic Impairment
• Liver Diseases

Intervention

Drug:
• Saroglitazar Magnesium 2 mg
1 tablet, single dose at Day 1
• Saroglitazar Magnesium 4 mg
1 tablet, single dose at Day 1

Locations

Country	Name	City	State
United States	Indiana University School of Medicine	Indianapolis	Indiana
United States	American Research Corporation at Texas Liver Institute	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Zydus Therapeutics Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	AUC from time zero to infinity (AUC0-8)	The area under the plasma concentration versus time curve from zero to infinity will be calculated by adding Ct/Kel to AUCt, where Ct is the last quantifiable concentration and Kel is the elimination rate constant.	Before dosing on Day 1 through Day 7
Primary	AUC from time zero to the last quantifiable concentration (AUC0-t)	The area under the plasma concentration versus time curve will be calculated using the linear trapezoidal rule from the zero time point to the last quantifiable concentration.	Before dosing on Day 1 through Day 7
Primary	Cmax	Maximum measured plasma concentration over the time span specified.	Before dosing on Day 1 through Day 7
Primary	Tmax	Time of the maximum measured plasma concentration.	Before dosing on Day 1 through Day 7
Primary	t1/2	The half-life will be calculated by the equation tHalf = 0.693/ Kel. Kel (The terminal elimination rate constant) will be obtained from the slope of the line, fitted by linear least squares regression, through the terminal points of the natural log of the concentration versus time plot for these points	Before dosing on Day 1 through Day 7
Primary	CL/F	Clearance	Before dosing on Day 1 through Day 7
Primary	Vz/F	Volume of distribution	Before dosing on Day 1 through Day 7
Secondary	Urine Pharmacokinetic: Ae	Amount of drug excreted during each collection interval	Before dosing on Day 1 through Day 5
Secondary	Incidence of AEs	Incidence and severity of AEs as a measure of safety and tolerability will be measured and reported.	Before dosing on Day 1 through Day 12
Secondary	Unbound Fraction	Unbound fraction in plasma of Saroglitazar	Day 1
Secondary	Unbound concentration	Unbound concentration in plasma of Saroglitazar	Day 1