Evaluate the Safety and Efficacy of Saroglitazar Magnesium in Patients With Fasting Triglyceride ≥500 mg/dL and ≤1500 mg/dL

SARO.15.001.04 is a multicenter, prospective, randomized, double-blind, placebo-controlled,
parallel arm, 12-week study designed to evaluate the safety and efficacy of Saroglitazar
Magnesium 1, 2 and 4 mg in patients with fasting triglyceride ≥500 mg/dL and ≤1500 mg/dL.

A total 124 subjects will be enrolled in a ratio of 1:1:1:1 to receive either Saroglitazar
Magnesium 1 mg, Saroglitazar Magnesium 2 mg, Saroglitazar Magnesium 4 mg, or placebo.

Inclusion Criteria:

1. Adults subjects (≥18 year) of either gender.

2. Average fasting TG-C ≥500 mg/dL and ≤1500 mg/dL (from Visits 2 and 2.1).

3. Able and willing to give written informed consent and comply with the requirements of
the study protocol.

Exclusion Criteria:

1. History of pancreatitis within 6 months of the initial screening visit (Visit 1);
patients that have an episode of pancreatitis after Visit 1 but before randomization
will not be randomized.

2. Patients with any history of pancreatitis may not be on GLP-1 agonists, DPP-4
inhibitors or pramlintide, with their last dose no sooner than 3 months prior to Visit
1; use of these agents by this population is prohibited throughout the duration of the
trial and follow-up period. [Patients without a history of pancreatitis on these
agents must be on a stable dose as of 3 months prior to Visit 1.]

3. History of >5% weight gain or weight loss or participation in weight gain/loss program
in past 3 months and not in the maintenance phase as of Visit 1.

4. Diabetic (as per ADA guideline) patients with HbA1c >9.5 %.

5. Patients on prandial/rapid acting insulin, thiazolidinediones (TZDs) or glitazars in
the 3 months prior to Visit 1.

6. Patients on unstable doses of basal insulin (i.e., glargine, detemir, NPH) with
unstable defined as a greater than 20% fluctuation in daily dose within the past 3
months.

7. Patients on anti-obesity medications within 6 months of Visit 1 (orlistat, lorcaserin,
phentermine, naltrexone/bupropion etc.).

8. Patients on drugs that may promote weight loss (i.e., anti-epileptic agents such as
topiramate, zonisamide and the anti-depressant bupropion) may not be taken, unless the
dose is stable for 3 months and the indication for use is not weight loss.

9. Patients on prohibited nutraceutical supplements contained in Annexure 1 that are
unwilling to wash-out starting at Visit 1 (and abstain from use throughout the
duration of the study, including follow-up).

10. Patients with unexplained hematuria prior to or first noted during Visit 1.

11. Patients with anemia who are undergoing repletion of deficiencies (iron, folate, B12)
not in the maintenance phase as of Visit 1.

12. Patients on concomitant lipid-lowering medications and not willing to participate in
Lead-in/Run-in Phase (Please refer Lead-in/Run-in Phase).

13. Patients having heart failure of NYHA class (III-IV), unstable angina, acute
myocardial infarction, stroke, transient ischaemic attack, any coronary
revascularisation procedure and hospitalization for acute coronary syndrome and
discharge within 6 months prior to screening.

14. Patients with Left Ventricular dysfunction (Left Ventricular Ejection Fraction (LVEF)
<40%, as measured through ECHO).

15. Uncontrolled hypertension (SBP >160 and/or DBP>100).

16. An uncontrolled thyroid disorder

- Uncontrolled hyperthyroidism is defined as any history of hyperthyroidism that
has either not been treated with either radioactive iodine (RAI) and/or surgery
-or- that has been treated with RAI and/or surgery, but has required ongoing
continuous or intermittent use of thyroid hormone synthesis inhibitors (i.e.,
methimazole or proplythiouracil) within 6 months of Visit 1.

- Uncontrolled hypothyroidism is defined as initiation of thyroid hormone
replacement therapy or dose adjustment of replacement therapy within 3 months of
Visit 1.

17. History of GI malabsorption or history of gastric bypass, banding, or diversional
bariatric surgery.

18. History of active liver disease or gall stones or hepatic dysfunction demonstrated by
AST and ALT ≥2 times of upper normal limit (UNL) or bilirubin ≥1.5 times UNL at Visit
1.

19. History of myopathies or evidence of active muscle diseases demonstrated by CPK ≥5
times UNL at Visit 1.

20. History of any other concurrent serious illness or malignancy (except successfully
treated basal and squamous cell carcinoma of the skin), within the past 5 years (e.g.
tuberculosis, HIV).

21. Positive HIV, hepatitis A (positivity of IgM), hepatitis B, or hepatitis C at Visit 1.

22. History of excessive consumption of alcoholic beverages (consumes >2 alcoholic drinks
per day or >14 alcoholic drinks per week, or engages in binge drinking). For the
remainder of the study, patients should agree to refrain from excessive alcohol
consumption (i.e., >2 alcoholic beverages per day), to maintain their current dietary
regimen, and to not alter their normal activity routines. (Note: patients should not
drink alcohol for at least 24 hrs prior to any site visit).

23. History of known allergy, sensitivity or intolerance to the study drugs and their
formulation ingredients.

24. Renal dysfunction demonstrated by abnormal eGFR <50 mL/min/1.73 m2.

25. History of clinically significant* systemic steroid therapy (intramuscular,
intravenous, intra-articular, or oral route) within 3 months of the Visit 1 or
anticipated requirement for systemic steroid therapy at Visit 1(however, topical,
ophthalmic and inhaled steroids are allowed).

* Clinically significant' (i.e., no more than 5 days of systemic steroids treatment
within 3 months of Visit 1)

26. NSAID use in excess of a reasonably prescribed dose and/or use in individuals with a
history of complications resulting from these agents.

27. Participation in any other clinical trial in the past 3 months in which
investigational product was taken and/or a medical device was utilized. Patients that
were screened but not randomized for another study must wait 30 days to participate in
Visit 1.

28. Pregnancy (including a positive urine and serum pregnancy test at Visit 1), lactation
or planned pregnancy/lactation during any time during the lead-in, study or follow-up
periods.

29. Patients on hormonal contraception or hormone replacement therapy containing estrogen
(progesterone based contraception and testosterone replacement therapy are permitted
granted that dosing is stable for at least 3 months prior to Visit 1).

30. Women of childbearing potential (WOCBP) and men, UNLESS using effective contraceptive
methods, such as an intra-uterine device or other mechanical contraception method with
condom or diaphragm and spermicide) throughout the study. For male patients,
contraception measures (condom and spermicide) must be taken during the study, either
by the male participant or his female partner. (Note: Enrolled females otherwise must
be surgically sterilize for at least the 6 months preceding Visit 1 or postmenopausal,
defined as 12 months with no menses without an alternative medical cause).