Safety Pilot Study of Farnesoid X Receptor (FXR) Agonist in Non-alcoholic Fatty Liver Disease (NAFLD) Patients

Non Alcoholic Fatty Liver Disease Clinical Trial

Official title:

A Safety Pilot Study of Px-104 in Non-alcoholic Fatty Liver Disease (NAFLD) Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01999101
• Other study ID #: PHS-Px-104-II-01
• Status: Completed
• Phase: Phase 2
• First received: November 19, 2013
• Last updated: September 28, 2016
• Start date: October 2013
• Est. completion date: June 2016

Study information

• Verified date: November 2014
• Source: Phenex Pharmaceuticals AG
• Contact: n/a
• Is FDA regulated: No
• Health authority: Austria: Austrian Medicines and Medical Devices Agency
• Study type: Interventional

Clinical Trial Summary

The primary aim of the study is to evaluate the safety and tolerability of Px-104 in NAFLD patients and to assess the influence of Px-104 on hepatic fat.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: June 2016
• Est. primary completion date: January 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• NAFLD patients

• Weight > 65 kg

• BMI > 25 and < 40

• Negative blood or urine pregnancy test (for females of childbearing potential) collected at screening followed by another negative serum pregnancy test collected within 24 hours prior to the first dose of study drug.

• Contraception: Female patients must be postmenopausal, surgically sterile, or if premenopausal, must be prepared to use at least two effective (=1% failure rate) method of contraception during the course of the study and for 14 days after the end of dosing. Male patients with female partners of child bearing potential must be prepared to use at least two effective methods of contraception with all sexual partners unless they have had a prior vasectomy

• Must be willing and able to give written informed consent and agree to comply with the study protocol.

• Sinus rhythm in 12-lead ECG

Exclusion Criteria:

• Evidence of excessive alcohol, drug or substance abuse (excluding marijuana use) within 1 year of first dose.

• History or other evidence of a medical condition associated with chronic liver disease other than.

• History or other evidence of decompensated liver disease (Child-Pugh Grade B or higher), coagulopathy, hyperbilirubinemia, hepatic encephalopathy, hypoalbuminemia, ascites, hepatic encephalopathy, and bleeding from esophageal varices are conditions consistent with decompensated liver disease.

• Concomitant intake of fibrates or statins (at least 4-6 weeks before start; considering half life of medication).

• Any clinically relevant findings in ECG (identified via 24h-Holter ECG or 12-Lead ECG) at screening

• History of any structural cardiac disease.

• In addition, patients with documented or presumed unstable coronary artery disease, stable or unstable cardiovascular disease or cerebrovascular disease.

• One or more of the following conditions: (1) poorly controlled hypertension, OR (2) screening or baseline blood pressure = 160 mmHg for systolic OR (3) screening or baseline blood pressure = 100 mmHg for diastolic blood pressure.

• Type I or II diabetes with HbA1C > 6.5% at screening and/or fasting plasma glucose > 7mmol/L (> 126 mg/dl).

• History or other evidence of a clinically relevant ophthalmologic disorder due to diabetes mellitus or hypertension or history or other evidence of severe retinopathy (e.g., cytomegalovirus, macular degeneration).

• Known sensibility to any ingredients contained in the investigational medicinal product (IMP)

• All conditions that do not allow magentic resonance (MR) assessments

• History of having received any investigational drug = 3 months and/or 6 x half-life prior to the first dose of study drug or the expectation that such drugs will be used during the study. Patients enrolled in this study cannot be enrolled in another study for either research, diagnostic or treatment purposes.

• Woman with childbearing potential unless using adequate contraception (see inclusion criteria); females who are pregnant or breast feeding.

• History of severe allergic

• Evidence of an active or suspected cancer, or a history of malignancy within the last 2 years, with the exception of patients with basal cell carcinoma that has been excised and cured.

• History of any systemic anti-neoplastic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) 6 months prior to the first dose of study drug or the expectation that such treatment will be needed at any time during the study.

• History of bleeding disorders or anticoagulant use

• History or other evidence of chronic pulmonary disease associated with functional limitation.

• History of uncontrolled severe seizure disorder.

• Poorly controlled thyroid dysfunction.

• History of major organ transplantation with an existing functional graft.

• Any signs of acute infection or inflammation

• History or other evidence of severe illness, or any other conditions which would make the patient, in the opinion of the investigator, unsuitable for the study.

• Any herbal supplements containing silymarin, tocopherol, vitamin C, riboflavins, proflavins, curcumin. (at least 4-6 months before the study)

• Positive test at screening for anti-Hepatits A virus (HAV) Immunoglobulin M (IgM), Hebatitis B surface antigen (HBsAg), Anti-Hepatits B core Antigen Immunglobulin M antibody (anti-HBc IgM Ab), or anti-HIV Ab.

• Subjects who have undergone surgery within the last 3 months.

• Subjects who have had a prior gastrointestinal surgery.

• Subjects who will be unavailable for the duration of the trial, who are unlikely to be compliant with the protocol, or who are felt to b unsuitable by the investigator for any other reason

• Imprisonment

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Fatty Liver
• Liver Diseases
• Non Alcoholic Fatty Liver Disease
• Non-alcoholic Fatty Liver Disease

Intervention

Drug:
• Px-104
28 days treatment

Locations

Country	Name	City	State
Austria	Division of Gastroenterology and Hepatology, Department of Internal Medicine III	Vienna

Sponsors (2)

Lead Sponsor	Collaborator
Phenex Pharmaceuticals AG	Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Changes in the Saccharose-Lactulose-Mannitol + Sucralose (SLM+S) Test to evaluate the intestinal permeability	Measurement of urinary concentrations of Saccharose, Lactulose, Mannitol and Sucralose by HPLC	baseline and day 27	No
Other	Assessment of liver steatosis by CAP-Fibroscan	Measurement of hepatic fat (%) by CAP-Fibroscan	baseline and day 28	No
Primary	Safety	Analysis of clinical chemistry, hematology, and assessment of clinical signs and adverse events over 28 days. Change day 28 vs. day 1	28 days	Yes
Secondary	Change of hepatocellular lipid content	Measurement of hepatic fat (%) by Magnetic resonance spectroscopy (MRS), change day 28 vs. day 1	day 1 and day 28	No
Secondary	Changes in oral glucose tolerance test (oGTT)	Measurement of plasma glucose level (mg/dL)	baseline and day 27	No
Secondary	Change from baseline in fibroblast growth factor 19 (FGF-19)	Measurement by ELISA (pg/mL)	days 1, 7, 14, 21 and 28	No
Secondary	Change from baseline in plasma bile acid concentration	Assessment by LC-MS/MS (µmol/L)	days 1, 7, 14, 21, and 28.	No
Secondary	Pharmacokinetics of Px-104 and conjugates	Measurement by LC-MS/MS (ng/mL). AUC, Cmax and other pk parameters	day 1 and day 28	No