A Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of HPN-01 in Healthy Subjects

Non-Alcoholic Steatohepatitis (NASH) Clinical Trial

Official title:

A Randomized, Double-Blind, Placebo Controlled, Sequential Parallel Group, Single and Multiple Ascending Doses (SAD/MAD) Study Following Oral Administration in Healthy Subjects to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HPN-01

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04481594
• Other study ID #: HPN-01-US-101
• Status: Recruiting
• Phase: Phase 1
• Start date: September 8, 2020
• Est. completion date: July 2021

Study information

• Verified date: February 2021
• Source: Hepanova Inc.
• Contact: Michelle Pluviose, MS
• Phone: 201-416-7763
• Email: mpluviose[@]frontagelab.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a randomized, double-blind, placebo-controlled first-in-human study in which the safety, tolerability, pharmacokinetics and pharmacodynamics of orally administered HPN-01 will be evaluated in healthy subjects

Description:

This study aims to obtain safety, tolerability, pharmacokinetic and pharmacodynamic data when HPN-01 is orally administered as single doses and as multiple doses to healthy subjects. The study will be conducted in 2 parts: a single ascending dose (SAD) phase (Part 1) and a multiple ascending dose (MAD) phase (Part 2). One cohort of Part 1 will receive HPN-01 after a standard high fat/high calorie breakfast (the fed condition) to investigate the effect of food on the pharmacokinetics of HPN-01.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 72
• Est. completion date: July 2021
• Est. primary completion date: July 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Are capable of giving informed consent and complying with study procedures;

2. Are between the ages of 18 and 55 years, inclusive;

3. Female subjects have a negative pregnancy test result at screening and admission to

the study site, and meet one of the following criteria:

1. Using a medically acceptable form of birth control for at least 1 month prior to screening (3 months on oral contraceptives) [e.g., hormonal contraceptives (oral, patch, injectable or vaginal ring), implantable device (implantable rod or intrauterine device), or a double barrier (e.g., diaphragm, cervical cap, oral, patch or vaginal hormonal contraceptive, condom, spermicide, or sponge)]

2. Surgically sterile for at least 3 months prior to screening by one of the

following means:

• Bilateral tubal ligation
• Bilateral salpingectomy (with or without oophorectomy)
• Surgical hysterectomy
• Bilateral oophorectomy (with or without hysterectomy)

3. Postmenopausal, defined as the following:

• Last menstrual period greater than 12 months prior to screening
• Postmenopausal status confirmed by serum FSH and estradiol levels at screening;

4. Considered healthy by the Investigator, based on subject's reported medical history, full physical examination, clinical laboratory tests, 12-lead ECG, and vital signs;

5. Normal renal function (eGFR > 90 ml/min/1.75 m2) as determined by Investigator following review of clinical laboratory test results;

6. Non-smoker and has not been exposed to any products containing nicotine in the last 6 months;

7. Body mass index (BMI) of 18.0 to 32.0 kg/m2 inclusive and body weight not less than 50 kg;

8. Willing and able to adhere to study restrictions and to be confined at the clinical research center;

9. Male subjects must agree to utilize a highly effective method of contraception (condom plus spermicide) during heterosexual intercourse from clinic admission until 12 weeks following the end of study visit;

10. Male subjects with female partners of child-bearing potential must agree to use condoms for the duration of the study and until 12 weeks after dosing with the study drug and must refrain from donating sperm for this same period.

Exclusion Criteria:

1. Clinically significant history of gastrointestinal, cardiovascular, musculoskeletal, endocrine, hematologic, psychiatric, renal, hepatic, bronchopulmonary, neurologic, immunologic, lipid metabolism disorders, or drug hypersensitivity as determined by the Investigator;

2. Known or suspected malignancy;

3. Reported history of pancreatitis or gall stones;

4. Reported history of unexplained syncope, symptomatic hypotension or hypoglycemia;

5. Family history of long QTc syndrome;

6. History of chronic diarrhea, malabsorption, unexplained weight loss, food allergies or intolerance;

7. Poor venous access;

8. Positive blood screen for human immunodeficiency virus (HIV), hepatitis B core (IgG and IgM) and surface antigen (HBsAg), Hepatitis A antibody (IgM), hepatitis C antibody (IgG), or hepatitis E (IgG and IgM) at Screening;

9. Donated or lost >500 mL of blood in the previous 3 months prior to screening;

10. Taken an investigational drug or participated in a clinical trial within 3 months (or 5 half-lives) prior to first dose of study drug, whichever is longer;

11. Taken any prescription medications (with the exception of hormonal contraceptive) within 14 days or 5 half-lives (whichever is longer) of the first dose of study drug;

12. Hospital admission or major surgery within 6 months prior to screening;

13. A history of prescription drug abuse, or illicit drug use within 9 months prior to screening;

14. A history of alcohol abuse according to medical history (= 2 drinks per day for male and = 1 drink per day for female) within 9 months prior to screening;

15. A positive screen for alcohol, drugs of abuse at screening or admission;

16. An unwillingness or inability to comply with food and beverage restrictions during study participation;

17. Use of over-the-counter (OTC) medication within 7 days, and/or herbal medications (including St John's Wort, herbal teas, garlic extracts) within 7 days prior to first dose of study drug (Note: Use of acetaminophen at < 2 g/day is permitted until 24 hours prior to dosing);

18. Any condition or finding that in the Investigators opinion would put the subject or study conduct at risk if the subject were to participate in the study.

Related Conditions & MeSH terms

• Fatty Liver
• Non-alcoholic Fatty Liver Disease
• Non-Alcoholic Steatohepatitis (NASH)

Intervention

Drug:
• HPN-01
25 mg, 50 mg, 100 mg, 150 mg, 200 mg and 300 mg HPN-01 capsules
• Placebo
25 mg, 50 mg, 100 mg, 150 mg, 200 mg and 300 mg HPN-01 placebo capsules

Locations

Country	Name	City	State
United States	Frontage Clinical Services, Inc	Secaucus	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Hepanova Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Single-dose PK Parameter	Cmax of HPN-01	Up to 72 hours postdose
Primary	Single-dose PK Parameter	AUClast of HPN-01	Up to 72 hours postdose
Primary	Single-dose PK Parameter	AUCinf of HPN-01	Up to 72 hours postdose
Primary	Multiple-dose PK Parameters	Cmax of HPN-01	Up to 24 hours postdose
Primary	Multiple-dose PK Parameters	Ctau of HPN-01	Up to 24 hours postdose
Primary	Multiple-dose PK Parameters	AUCtau of HPN-01	Up to 24 hours postdose
Primary	Incidence of Adverse Events		Up to 15 days plus 6 days
Primary	Proportion of Participants with 12-lead ECG Abnormalities		Up to 15 days plus 6 days
Primary	Proportion of Participants with Clinical Laboratory Abnormalities		Up to 15 days plus 6 days
Secondary	Measurement of PD Biomarker Level of Fibroblast Growth Factor 19 (FGF19) Following Oral Single and Multiple Ascending Dose Administration		Up to 24 hours postdose
Secondary	Measurement of PD Biomarker Level of C4 Following Oral Single and Multiple Ascending Dose Administration		Up to 24 hours postdose