Overview

FM101 Efficacy Study in Adults With Nonalcoholic Fatty Liver Disease or Nonalcoholic Steatohepatitis

Status:
Recruiting
Trial end date:
2022-07-03
Target enrollment:
0
Participant gender:
All
Summary
A Randomized Phase 2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of FM101 in Adults with Nonalcoholic Fatty Liver Disease or Nonalcoholic Steatohepatitis
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Future Medicine
Criteria
Inclusion Criteria:

Individuals must meet all of the following criteria to be included in the study:

1. Be able and willing to provide written informed consent to take part in the study, and
to comply with all the study's requirements.

2. Be a man or woman ≥18 years of age at screening.

3. Have c. Histologic confirmation of NASH no more than 12 months before the screening
visit date, demonstrating the existence of steatosis ≥5%, hepatocyte ballooning and
chronic inflammation (at least 1 point for each component), and stage 1 through stage
3 liver fibrosis according to the NASH Clinical Research Network (CRN); OR d. NAFLD
based upon demonstration of at least 3 of the following 5 components of the metabolic
syndrome below, at screening:

- Fasting plasma glucose ≥100 mg/dL , or undergoing drug treatment for elevated
plasma glucose concentrations

- High-density lipoprotein-cholesterol (HDL-c) concentration <40 mg/dL in male
patients, or <50 mg/dL in female patients, or undergoing drug treatment for
reduced serum HDL-c concentrations

- Serum triglyceride (TG) concentration ≥150 mg/dL, or undergoing drug treatment
for elevated serum TG concentrations

- Waist circumference >102 cm in male patients or >88 cm in female patients

- Systolic blood pressure ≥130 mm Hg or diastolic blood pressure ≥85 mm Hg, or
undergoing drug treatment for hypertension, or antihypertensive drug treatment in
a patient with a history of systemic hypertension

4. Serum ALT concentration >1 × upper limit of normal (ULN) at screening

5. Undergo MRI-PDFF that demonstrates ≥8% liver steatosis during the screening period.

6. Undergo MRE with a score ≥2.9 kPa during the screening period.

7. Women of childbearing potential (WoCBP) must have a negative serum beta human
chorionic gonadotropin (HCG) test result at screening.

Female patients must agree to use highly effective birth control throughout the study
and up to 30 days after the last dose of study drug has been taken. Highly effective
contraception measures include the following, but not limited to:

- Combined estrogen- and progestogen-containing hormonal contraception (oral,
intravaginal and transdermal);

- Progestogen-only hormonal contraception associated with inhibition of ovulation
(oral, injectable, and implantable);

- Intrauterine device, intrauterine hormone-releasing system, bilateral tubal,
occlusion ('tubal occlusion' includes 'tubal ligation');

- Vasectomized partner (only in the event that the vasectomized partner is the sole
sexual partner of the WoCBP);

- Sexual abstinence (defined as refraining from heterosexual intercourse) only in
the event that this is the preferred lifestyle of the patient.

Childbearing potential is defined as being fertile following menarche and until
becoming postmenopausal unless permanently sterile (hysterectomy, bilateral
salpingectomy, or bilateral oophorectomy).

A postmenopausal state is defined as no menses for ≥12 consecutive months without an
alternative medical cause.

Men with partners who are WOCBP must either be surgically sterile or agree to use a
barrier contraceptive for the duration of the study and up to 30 days after the last
dose of study drug.

8. Be willing to maintain a stable diet, including alcohol intake this applies, and
physical activity throughout the entire study.

Exclusion Criteria:

Individuals meeting any of the following criteria at screening or baseline are ineligible
to participate in this study:

1. Any patient who refuses to provide written informed consent to take part in the study,
and/or appears unwilling to comply with study-specific requirements.

2. Female persons who are pregnant, or are breastfeeding at screening, or who plan to
become pregnant during the study.

3. Body mass index (BMI) <25 kg/m2.

4. Fibrosis-4 index (FIB-4) >2.6 at screening.

5. Any of the following laboratory test abnormalities at screening:

1. Serum ALT and/or AST concentration >5 × upper limit of normal (ULN)

2. Total serum bilirubin (BR) concentration >ULN; if an established diagnosis of
Gilbert's syndrome exists and the direct serum BR result at screening is less
than or equal to ULN the patient may participate in the study

3. Serum albumin concentration ≤3.5 g/dL

4. International normalized ratio (INR) ≥1.3

5. Platelet count less than the lower limit of normal range (LLN)

6. Creatinine clearance rate <60 mL/minute as calculated by the modification of diet
in renal disease (MDRD) estimated glomerular filtration rate (eGFR) equation

7. Positive COVID-19 polymerase chain reaction (PCR) test result at screening NOTE:
Repeat testing of a given parameter or parameters that returned ineligible
results, may be performed during the same screening period in consultation with
the sponsor's Medical Monitor. An interval of at least 7 days should exist
between receipt of the ineligible test result and re-testing.

6. Chronic liver disease other than confirmed or suspected NASH, including but not
limited to the following diagnoses / entities:

1. Chronic hepatitis B virus infection (defined by the presence of hepatitis B
surface antigen at screening) and / or chronic hepatitis C virus (HCV) infection
(defined by the presence of detectable HCV ribonucleic acid (RNA) antibody
[anti-HCV] at screening). Patients whose anti-HCV antibody test at screening is
positive, but who test negative for HCV RNA at screening will be permitted to
participate in the study as long as there has been evidence of viral negativity
for at least 24 months prior to screening)

2. Autoimmune hepatitis (AIH), or confirmed overlap syndrome of AIH and either
primary biliary cholangitis or primary sclerosing cholangitis.

3. Primary biliary cholangitis, primary sclerosing cholangitis, secondary sclerosing
cholangitis whatever the basis for this, e.g. chronic pancreatitis resulting in
bile duct stricture formation, recurrent extrahepatic bile duct calculus
formation, arterial insult resulting in bile duct stricture formation

4. Wilson's disease, homozygous alpha-1-anti-trypsin deficiency, hemochromatosis,
drug-induced liver disease

5. Alcoholic liver disease

6. Suspected or confirmed hepatocellular carcinoma

7. Medical, histologic, and/or imaging history of hepatic cirrhosis.

8. Clinical, endoscopic, imaging and/or laboratory manifestations of portal hypertension,
such as spider nevi, splenomegaly, clinically evident ascites formation, non-bleeding
gastro-oesophageal varices.

9. Known history of human immunodeficiency virus (HIV) infection.

10. Chronic use (≥12 months) of any drug known to be associated with development of NAFLD
during the five years before the anticipated Day 1 visit date, e.g. amiodarone,
methotrexate, systemic glucocorticoids (unless employed at physiologic replacement
doses for management of confirmed adrenal insufficiency), tetracyclines, tamoxifen,
estrogens at doses greater than those used for hormone replacement therapy, anabolic
steroids (other than testosterone replacement preparations being taken at a
physiologic replacement dose for management of confirmed male hypogonadism), sodium
valproate, and other hepatotoxins, e.g. minocycline.

11. Use of the following medications:

1. GLP-1 agonists, unless on a stable dose for at least 3 months prior to screening

2. Thiazolidinediones, obeticholic acid or vitamin E at a daily dose >400 IU daily
within the 6 months before screening

3. Statin therapy and other lipid-modifying therapies must have been used at a
stable dose for ≥3 months prior to screening

4. Oral antidiabetic medication(s) (other than those specifically excluded) must
have been used / taken at a stable daily dose for ≥3 months prior to screening

12. History of significant alcohol consumption, defined as an average of >20 g/day in
female patients and >30 g/day in male patients, for a period of >3 consecutive months
within 1 year prior to screening, hazardous alcohol use (Alcohol Use Disorders
Identification Test score ≥8), or an inability to reliably quantify alcohol
consumption based upon judgment of the investigator.

13. Active substance abuse within the 1 year before the screening visit date, upon the
judgement of the investigator.

14. Weight change ≥7% within the 6 months prior to screening or ≥5% within the 3 months
prior to screening.

15. Prior or planned (during the study period) weight reduction surgery, e.g. sleeve
gastrectomy, Roux-en-Y gastrojejunostomy.

16. Type 1 diabetes mellitus by medical history.

17. Poorly controlled type 2 diabetes mellitus (this is defined as hemoglobin A1c (HbA1c)
>9.5% at screening, or a patient whose oral anti-diabetic medication dosing requires
adjustment >10% less than 2 months before the screening visit date.

18. Uncontrolled systemic hypertension (either treated or untreated) defined as systolic
blood pressure >160 mmHg or a diastolic blood pressure >100 mmHg at screening. A
retest of blood pressure, (after establishing good blood pressure control within a
reasonable period of time and up to the Baseline visit) is permissible at the
discretion of the Investigator.

19. Patients who demonstrate recent evidence (within 6 months of the anticipated date of
the Day 1 visit) of clinically evident and significant atheromatous cardiovascular
disease, e.g. unstable angina, acute coronary syndrome, myocardial infarction,
cerebrovascular accident [stroke], cerebrovascular ischemia, transient ischemic
attack, and / or peripheral vascular disease requiring intervention.

20. Has taken part in a clinical trial and been administered an active investigational
product being evaluated for the treatment of NASH, weight reduction and / or type 2
diabetes mellitus, during the 6 months prior to the anticipated Day 1 visit date.

21. Has participated in an investigational new drug trial during the 30 days prior to
screening visit date, or within 5 half-lives of an investigational agent, whichever is
longer.

22. Has a confirmed diagnosis of malignancy within 5 years prior to screening, except for
basal- or squamous-cell carcinoma of the skin that has been treated successfully, or
cervical carcinoma in situ that has been treated successfully. Patients with a history
of other malignancies that have been treated with curative intent and who have no
demonstrable disease recurrence within 5 years prior to screening may also be eligible
if approved following discussion with the Sponsor's Medical Monitor. Patients under
evaluation for malignant disease currently are not eligible for study participation.

23. Patients who are unable to undergo MRI studies, whatever the reason for this, e.g.
claustrophobia, the presence of a device or implant that would make imaging dangerous
for the patient.

24. Any other condition which, in the opinion of the Investigator, would impede compliance
with, hinder completion of the study, compromise the well-being of the patient, and /
or interfere with the study's endpoints.