Saroglitazar Magnesium for Treatment of Primary Biliary Cholangitis

Overview

Saroglitazar Magnesium 1 mg and 2 mg tablets for treatment of subjects with Primary Biliary Cholangitis (PBC)

Description

A Multicenter, Randomized, Double-blind, Placebo controlled, Phase 2b/3 Study to Evaluate the Efficacy and Safety of Saroglitazar Magnesium in Subjects with Primary Biliary Cholangitis

Eligibility

Inclusion Criteria:

1. Males or females, between 18 and 75 years of age, both inclusive at screening.
2. Subjects on ursodeoxycholic acid (UDCA) for at least 12 months at a therapeutic dose (at least 13 mg/kg per day) and a stable dose for 6 months prior to Screening Visit and having ALP ≥ 1.67 x ULN.

   OR Subjects who are unable to tolerate UDCA and did not receive UDCA for at least 3 months prior to the date of screening and having ALP ≥ 1.67 x ULN.

3. History of confirmed PBC diagnosis, based on American Association for the Study of Liver Disease [AASLD] and European Association for Study of the Liver [EASL] Practice Guidelines, as demonstrated by the presence of at least ≥ 2 of the following 3 diagnostic factors:
   • History of elevated ALP levels for at least 6 months prior to screening
   • Positive anti-mitochondrial antibodies (AMA) titer OR positive PBC specific antibodies (anti-GP210 and/or anti-SP100 and/or antibodies against the major M2 components [PDC-E2, 2-oxo-glutaric acid dehydrogenase complex]) if AMA is negative
   • Liver biopsy consistent with PBC
4. ALP ≥ 1.67 x ULN at both Visits 1 and 2 and < 30% variance between the levels from

   Visit 1 to Visit 2

5. Total bilirubin < 2 x ULN at screening (Visit 1)
6. Must provide written informed consent and agree to comply with the trial protocol.

Exclusion Criteria:

1. Consumption of 2 standard alcohol drinks per day if male and 1 standard alcohol drink per day if female for at least 3 consecutive months (12 consecutive weeks) within 5 year before screening (Note: 1 unit = 12 ounces of beer, 4 ounces of wine or 1 ounce of spirits/hard liquor).
2. History or presence of other concomitant liver diseases at screening:
   1. Chronic hepatitis B or C virus (HBV, HCV) infection. (Note: However, If the subject has been treated for the HCV infection and has been cured for a duration of more than 2 years from screening, such subjects can be enrolled in the study)
   2. Primary sclerosing cholangitis (PSC).
   3. Alcoholic liver disease.
   4. Autoimmune hepatitis (AIH) indicative of PBC with overlap syndrome.

        Note: The Paris criteria are commonly used to define the presence of PBC with features of
        AIH and have been endorsed by EASL and AASLD. According to these criteria, a diagnosis can
        be made in a patient with PBC as follows:
        At least two of the following:
        I. ALP > 2 x ULN or GGT > 5 x ULN. II. AMA positive III. Florid bile duct lesion on
        histology. AND
        At least two of the following three features:
        I. ALT > 5 x ULN. II. Immunoglobulin G serum levels > 2 x ULN or smooth muscle autoantibody
        positive.
        III. Moderate to severe interface hepatitis on histology. e. Hemochromatosis. f.
        Non-alcoholic steatohepatitis (NASH) on historical biopsy. 3.Cirrhosis with complications,
        including history or presence of: spontaneous bacterial peritonitis, hepatocellular
        carcinoma, ascites requiring treatment, encephalopathy, known large esophageal varices or
        history of variceal bleeding within one year prior to screening or history of hepatorenal
        syndrome.
        5.Medical conditions that may cause non-hepatic increases in ALP (e.g., Paget's disease) or
        which may diminish life expectancy to < 2 years, including known cancers.
        6.Use of thiazolidinediones or fibrates (within 12 weeks prior to screening). 7.Use of
        obeticholic acid (OCA), azathioprine, cyclosporine, methotrexate, mycophenolate,
        pentoxifylline, budesonide and other systemic corticosteroids (Note: Prednisone dose should
        not be more than 10 mg per day); potentially hepatotoxic drugs (including α-methyl-dopa,
        sodium valproic acid, isoniazid, or nitrofurantoin) (within 12 weeks prior to screening).
        9.History of bowel surgery (gastrointestinal [bariatric] surgery in the preceding 1 year or
        undergoing evaluation for gastrointestinal surgery (bariatric surgery for obesity,
        extensive small-bowel resection) or orthotopic liver transplant (OLT) or listed for OLT.
        10.Type 1 diabetes mellitus. 11.Unstable cardiovascular disease, including:
        a. Unstable angina, (i.e., new or worsening symptoms of coronary heart disease in the 12
        weeks before screening and throughout the Screening Period), acute coronary syndrome in the
        24 weeks before screening and throughout the Screening Period, acute myocardial infarction
        in the 12 weeks before screening and throughout the Screening Period or heart failure of
        New York Heart Association class (III - IV) or worsening congestive heart failure, or
        coronary artery intervention, in the 24 weeks before screening and throughout the Screening
        Period.
        b. History/current unstable cardiac dysrhythmias. c. Uncontrolled hypertension at
        screening. d. Stroke or transient ischemic attack in the 24 weeks before screening.
        12.History of intracranial hemorrhage, arteriovenous malformation, bleeding disorder,
        coagulation disorders, or screening blood tests that, in the opinion of the Investigator,
        indicate altered coagulability (e.g., PT, INR, aPTT) at screening.
        13.An uncontrolled thyroid disorder
          1. Uncontrolled hyperthyroidism: defined as any history of hyperthyroidism that has
             either not been treated with either radioactive iodine and/or surgery or that has been
             treated with radioactive iodine and/or surgery, but has required ongoing continuous or
             intermittent use of thyroid hormone synthesis inhibitors (i.e., methimazole or
             propylthiouracil) in the 24 weeks before screening.
          2. Uncontrolled hypothyroidism: defined as initiation of thyroid hormone replacement
             therapy or dose adjustment of replacement therapy in the 12 weeks before screening.
             14.History of myopathies or evidence of active muscle disease demonstrated by CPK ≥ 5
             x ULN at screening.
             15.Subjects whose ALT, AST, or ALP exceeds by more than 50% on Visit 2 reading
             compared to Visit 1. Note: If the ALT, AST, or ALP values on Visit 2 exceed by more
             than 50% from Visit 1, then a third value will be measured (within 1- 2 weeks) to
             assess for the trend. If the third value shows continued increase ≥ 10%, then subject
             is considered ineligible for randomization.
             16.Any of the following laboratory values at screening:
        a. Platelets < 50 × 109/L b. Albumin < 2.8 g/dL c. eGFR < 45 mL/min/1.73 m2 d. ALP > 10 x
        ULN e. ALT or AST > 250 U/L 17.Participation in another interventional clinical study and
        receipt of any other investigational medication (within 12 weeks prior to randomization up
        to end of study).
        18.History of malignancy in the past 5 years and/or active neoplasm with the exception of
        resolved superficial non-melanoma skin cancer.
        19.Contraindications to Saroglitazar Magnesium or has any conditions affecting the ability
        to evaluate the effects of Saroglitazar Magnesium.
        20.Known allergy, sensitivity, or intolerance to the study drug, comparator, or formulation
        ingredients.
        21.Pregnancy-related exclusions, including:
        a. Pregnant/lactating female (including positive pregnancy test at screening). b. Pregnancy
        should be avoided by male and female subjects either by true abstinence or the use of an
        acceptable effective contraceptive measures for the duration of the study and for at least
        1 month after the end of the study treatment. Refer Appendix 8 Contraceptive Guidance
        22.History or other evidence of severe illness or any other conditions that would make the
        subject, in the opinion of the Investigator, unsuitable for the study (such as poorly
        controlled psychiatric disease, HIV, coronary artery disease, or active gastrointestinal
        conditions that might interfere with drug absorption).
        23.Cirrhosis with Child-Pugh-Turcotte (CPT) Class B or C having score of 7 or above at
        screening 24.Subjects with Model for End Stage Liver Disease (MELD 3.0) score of 12 or
        above