DDI Study of ASC41 in HV and the PK, Safety and Tolerability in Subjects With NAFLD.

• Status: Completed
• Trial end date: 2021-06-10
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective of this study is to evaluate the effect of itraconazole, a strong inhibitor)of cytochrome P4503A , and phenytoin a strong inducer of cytochrome P450 3A, CYP3A4, CYP1A2 and CYP2C19 on the pharmacokinetics of ASC41, a THR beta agonist tables in healthy subjects. The PK, Safety and Tolerability of ASC 41 in Subjects with NAFLD will also be evaluated. Approximately 24 subjects including 16 healthy volunteers (HVs) and 8 subjects with NAFLD will be enrolled. This study consists of 3 cohorts.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Gannex Pharma Co., Ltd.
• Treatments: Itraconazole; Phenytoin

Criteria

Key Inclusion Criteria:

• Part I Healthy subjects between 18 to 55 years of age

• Part II

1. Subjects with NAFLD

2. Subjects between 18 to 65 years of age

Key Exclusion criteria:

• Part I

1. A history of thyroid disease

2. A history of, or current liver disease, or liver injuries

3. Platelet count <150,000/mcL

4. INR> 1.2

5. History of, or current electrocardiogram (ECG) abnormalities, arrhythmias or heart valve diseases judged to be clinically significant by the investigator

• Part II

1. A history of thyroid disease

2. Current or history of cirrhosis or decompensated liver disease

3. AST or ALT > 5X ULN

4. DBIL > ULN

5. Acute or chronic liver disease other than NAFLD

6. A history of bariatric surgery

7. HbA1c >9.5% at screening

8. Testosterone or estrogen replacement therapy

9. Inducers or inhibitors of CYP3A4, including herbal therapies such as St John's Wort (CYP3A4 Inducer)