Overview

PK Study Comparing Metformin Eicosapentaenoate to a Combined Dose of Metformin Hydrochloride and Ethyl Ester EPA

Status:
Unknown status
Trial end date:
2014-07-01
Target enrollment:
0
Participant gender:
All
Summary
The primary objective of the study is to contrast the pharmacokinetic profiles of metformin and EPA delivered separately as co-administered products (metformin hydrochloride or Glucophage and icosapent ethyl or Vascepa) and together as the solid dose form (metformin eicosapentaenoate or TP-101) under fasted and fed conditions. A secondary objective is to evaluate the safety and tolerability of single and repeat single doses of TP-101.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Thetis Pharmaceuticals LLC
Treatments:
Eicosapentaenoic acid ethyl ester
Metformin
Criteria
Inclusion Criteria:

- Signed informed consent executed prior to protocol screening assessments;

- Men or women 18 to 65 years of age, inclusive (Women may be surgically sterile via
tubal ligation, bilateral oophorectomy or hysterectomy or who are postmenopausal for
>1 year. Women who are of childbearing potential must agree to practice adequate
contraception one month before the first dose of study medication and up to Day 16 of
the study. Adequate contraception may include, but is not limited to, abstinence,
monogamous relationship with vasectomized partner, barrier methods such as condoms or
diaphragms with spermicide or foam, intrauterine devices, and licensed hormonal
methods.);

- No history of chronic diseases, except for subjects with well-controlled hypertension
or well-controlled hyperlipidemia;

- BMI ≤30kg/m2;

- No significant medical history including diabetes or hypertension complicated by
hyperlipidemia (metabolic syndrome);

- Negative urine drug and alcohol tests at Screening; and,

- No metformin or omega-3 products within 2 months.

Exclusion Criteria:

- Abnormal findings on physical examination, EKG, vital signs, and clinical laboratory
testing, in the judgment of the investigator;

- Allergies to fish or shellfish;

- Impaired renal function (calculated eGFR <60 mL/min);

- Abnormal laboratory values for T3, T4 and TSH at the Screening Visit;

- Aspartate aminotransferase/alanine aminotransferase (AST/ALT) >2x upper limits of
normal (ULN) or serum bilirubin >1.5 mg/dL;

- Requirement of prescription medication within 14 days of the Screening Visit, with the
exception of prescription medications for the prevention of pregnancy, anti
hypertensives for hypertension, or statins for hyperlipidemia. Doses of one or two
anti-hypertensives and/or a statin must be stable for >1 month;

- Normal doses of over-the-counter medications, including vitamins are allowed but not
within 3 days of Visit 2 (first day of dosing);

- Current or history of abuse of alcohol or illicit drugs within the preceding year to
the Screening Visit;

- Participation in a dietary modification or an intensive weight loss program;

- Participation in another clinical trial of an investigational product within 3 months
prior to the Screening Visit;

- Smokers (use of tobacco in the past 3 months); or,

- Donation or loss of 400 mL blood or more in the last 8 weeks.