Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

A Study of Oral Insulin to Reduce Liver Fat Content in Type 2 Diabetes Patients With Nonalcoholic Steatohepatitis (NASH)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04616014
Recruitment Status : Not yet recruiting
First Posted : November 4, 2020
Last Update Posted : March 3, 2021
Sponsor:
Information provided by (Responsible Party):
Oramed, Ltd.

Brief Summary:
A Study to Assess the Safety and Potential of Oral Insulin to Reduce Liver Fat Content in Type 2 Diabetes Patients with Nonalcoholic Steatohepatitis (NASH)

Condition or disease Intervention/treatment Phase
Nonalcoholic Steatohepatitis (NASH) Drug: ORMD-0801 QD Drug: ORMD-0801 BD Phase 2

Detailed Description:
An Open-Label Multi-Center Study to Assess the Safety and Potential of Oral Insulin to Reduce Liver Fat Content in Type 2 Diabetes Patients with Nonalcoholic Steatohepatitis (NASH)

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Intervention Model Description: This is an open, multi-center study
Masking: None (Open Label)
Masking Description: Open Label
Primary Purpose: Treatment
Official Title: An Open-Label Multi-Center Study to Assess the Safety and Potential of Oral Insulin to Reduce Liver Fat Content in Type 2 Diabetes Patients With Nonalcoholic Steatohepatitis (NASH)
Estimated Study Start Date : March 2021
Estimated Primary Completion Date : October 2021
Estimated Study Completion Date : October 2021


Arm Intervention/treatment
ORMD-0801 QD
8 mg QD, daily, in the morning
Drug: ORMD-0801 QD
8 mg, QD
Other Name: Oral Insulin

ORMD-0801 BD
8 mg BD, daily in the morning and in the evening
Drug: ORMD-0801 BD
8 mg, BD
Other Name: Oral Insulin




Primary Outcome Measures :
  1. Number of participants with treatment-related adverse events. [ Time Frame: Week 12 ]
    Safety of Oral Insulin will be measured by the number of treatment-related adverse events according to CTCAE version 5.0


Secondary Outcome Measures :
  1. Percent change in liver fat content [ Time Frame: Screening(Baseline) and Week 12 ]
    The percent change in liver fat content measured by MRI-Proton Density Fat Fraction from baseline to week 12

  2. Percent change in liver fibrosis [ Time Frame: Screening, Week 0, and Week 12 ]
    Percent change in liver fibrosis as measured by FibroScan Elasticity in units of kilo Pascals (kPa)

  3. Percent change in liver steatosis [ Time Frame: Screening, Week 0, and Week 12 ]
    Percent change in liver steatosis as measured by FibroScan Controlled Attenuation Parameter (CAP) in units of dB/meter



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female aged 18-70 years.
  • BMI ≥25.
  • Known type 2 DM according to American Diabetic Association (one of the three needed): Fasting Plasma Glucose ≥126 mg/dl or 2h postprandial (PG) following 75g OGTT ≥200 mg/dl or HbA1c > 6.5%28 or on treatment with metformin only or metformin in addition to no more than two of the following medications sulfonylurea, DPP-4 inhibitors, GLP-1 receptor agonists, Thiazolidinediones (TZDs).
  • Diagnosis of NAFLD by non-invasive determination of hepatic steatosis grade S1, defined as hepatic steatosis>8%. by MRI- PDFF and CAP FibroScan ≥ 238 dB/m.
  • Liver enzyme abnormalities: ULN≤5 times.
  • Fibrosis score 21≤F≤3 as defined by FibroScan measurement (Liver stiffness measurement, LSM) of 6 ≤ LSM ≤ 12 kPa.
  • Signature of the written informed consent.
  • Negative urineserum pregnancy test at Screening study entry for women of childbearing potential (WCBP).
  • Women of childbearing potential (WCBP) must have a negative urine pregnancy test result prior to the start of the run-in period and at. initiation of A negative urine and serum pregnancy test must be obtained prior to active dosing. Males and females of childbearing potential must use two methods of contraception (double barrier method), one of which must be an acceptable barrier method from the time of screening to the last dosing study visit (22 weeks). Barrier methods of contraception include male condoms plus spermicide, diaphragm with spermicide plus male condom, cervical cap with spermicide plus male condom, or oral contraceptives. Acceptable methods of birth control include abstinence, oral contraceptives, surgical sterilization, vasectomy, the contraceptive patch, and the contraceptive ring. If a subject is not usually sexually active but becomes active, he or his partner should use medically accepted forms of contraception. Sperm donations will not be allowed for the duration of the study and for 90 days after the last dose of study drug.
  • Females of non-childbearing potential are defined as postmenopausal who a) had more than 24 months since last menstrual cycle with menopausal levels of FSH (FSH Level > 40), b) who are surgically menopausal (surgical sterility defined by tubal occlusion, bilateral oophorectomy, bilateral salpingectomy or hysterectomy).
  • For hypertensive patients, hypertension must be controlled by stable dose of anti-hypertensive medication for at least 2 months prior to screening (and the stable dose can be maintained throughout the study) with BP < 150/<95 mmHg
  • Patients previously treated with vitamin E (>400IU/day), Polyunsaturated fatty acid (>2g/day) or Ursodeoxycholic acid fish oil can be included if drugs are stopped at least 3 months prior to enrolment and up to the end of the study.
  • Glycaemia must be controlled (Glycosylated Hemoglobin A1C ≤8.5%) while any HbA1c increment should not exceed 1% during 6 months prior to enrolment).
  • Patients who are willing to participate in the study, have to have their own self-monitoring blood glucose devices.

Exclusion Criteria:

  • Patients with active (acute or chronic) liver disease other than NASH (e.g. viral hepatitis, genetic hemochromatosis, Wilson disease, alpha-1 antitrypsin deficiency, alcohol liver disease, drug induced liver disease) at the time of enrolment.
  • ALT or AST > 5 times ULN.
  • Abnormal synthetic liver function (serum albumin ≤3.5gm%, INR >1.3).
  • Known alcohol and/or any other drug abuse or dependence in the last five years.
  • Weight >120 Kg (264.6 lbs.).
  • Known history or presence of clinically significant, cardiovascular, gastrointestinal, metabolic (other than diabetes mellitus), neurologic, pulmonary, endocrine, psychiatric, neoplastic disorder or nephrotic syndrome.
  • History or presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs including bile salt metabolites (e.g. inflammatory bowel disease (IBD), previous intestinal (ileal or colonic) operation, chronic pancreatitis, celiac disease or previous vagotomy.
  • Weight loss of more than 5% within 6 months prior to enrolment.
  • History of bariatric surgery.
  • Uncontrolled blood pressure BP ≥150/≥95.
  • Non-type 2 DM (type 1, endocrinopathy, genetic syndromes etc.).
  • Patients with HIV.
  • Daily alcohol intake >20 g/day (2 units/day) for women and >30 g/day (3 units/day) for men.
  • Treatment with anti-diabetic medications other than metformin and more than two of the following medications sulfonylurea, DPP-4 inhibitors, GLP-1 receptor agonists, TZDs.
  • Metformin, fibrates, statins, not provided on a stable dose in the last 6 months.
  • Patients who are treated with valproic acid, Tamoxifen, methotrexate, amiodarone.
  • Chronic treatment with antibiotics (e.g. Rifaximin).
  • Homeopathic and/or Alternative treatments. Any treatment must be stopped before the screening period.
  • Uncontrolled hypothyroidism defined as Thyroid Stimulating Hormone >2X the upper limit of normal (ULN). Thyroid dysfunction controlled for at least 6 months prior to screening is permitted.
  • Patients with renal dysfunction: eGFR< 40 ml/min.
  • Unexplained serum creatinine phosphokinase (CPK) >3X the upper limit of normal (ULN). Patients with a reason for CPK elevation may have the measurement repeated prior to enrolment; a CPK retest > 3X ULN leads to exclusion.
  • Subjects meeting criteria for contraindication for MRI - including the following:

    • History of severe claustrophobia impacting ability to perform MRI during the study, even despite mild sedation/treatment with as anxiolytic.
    • Subjects with metal implants, devices, paramagnetic objects contained within the body and excessive or metal-containing tattoos.
    • Subjects unable to lie still within the environment of the MRI scanner or maintain a breath-hold for the required period to acquire images, even despite mild sedation/treatment with an anxiolytic.
  • Subject participated in a clinical research study involving a new chemical entity within 4 weeks of study entry.
  • Known allergy to soy.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04616014


Contacts
Layout table for location contacts
Contact: Miriam Kidron, PhD +972 50-766-5423 miriam@oramed.com
Contact: Meir Silver, Ph.D. +972-54-633-5855 meir@oramed.com

Sponsors and Collaborators
Oramed, Ltd.
Investigators
Layout table for investigator information
Study Chair: Miriam Kidron, PhD Oramed, Ltd.
Publications:
Layout table for additonal information
Responsible Party: Oramed, Ltd.
ClinicalTrials.gov Identifier: NCT04616014    
Other Study ID Numbers: ORA-D-N01B
First Posted: November 4, 2020    Key Record Dates
Last Update Posted: March 3, 2021
Last Verified: October 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Fatty Liver
Non-alcoholic Fatty Liver Disease
Liver Diseases
Digestive System Diseases
Insulin
Insulin, Globin Zinc
Hypoglycemic Agents
Physiological Effects of Drugs