Natural Soybean-derived Femarelle ®for Patients With Non Alcoholic Fatty Liver Disease

This is a Single -arm, open-label, before-and after exploratory trial of 90 days of Femarelle ® to improve NAFLD and the metabolic syndrome.

Ingestion of Femarelle will improve non alcoholic steatohepatitis and the metabolic syndrome in patients suffering from these conditions.

Subjects will receive treatment with Femarele 530 mg (1 capsule twice a day) for 90 days and will then be monitored off study treatment for an additional 4 weeks.

Study Overview

• Status: Withdrawn
• Conditions: Nash
• Intervention / Treatment: Drug: Femarelle

• Study Type: Interventional
• Phase: Phase 4

Contacts and Locations

Study Locations

• Israel
  • Jerusalem, Israel, 91120
    • Hadassah Medical Organization, Jerusalem, Israel

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Biopsy proven NASH
2. If suffering from diabetes may be treated by up to 2 oral medications, with stable doses for 2 months.

3. If participating in sexual activity that could lead to pregnancy, the study volunteer must agree that two reliable methods of contraception will be used simultaneously while receiving the protocol-specified medication and for 1 month after stopping the medication.

   NOTE: Hormonal-based methods alone are not sufficient. At least two of the following methods MUST be used appropriately unless documentation of menopause, sterilization, or azoospermia is present:

   • Condoms (male or female) with or without a spermicidal agent. - Condoms are recommended because their appropriate use is the only contraception method effective for preventing HIV transmission
   • Diaphragm or cervical cap with spermicide
   • IUD
   • Hormonal-based contraception

   Study subjects who are not of reproductive potential (girls who have not reached menarche or women who have been post-menopausal for at least 24 consecutive months or have undergone hysterectomy and/or bilateral oophorectomy are eligible without requiring the use of contraceptives. Written or oral documentation communicated by clinician or clinician's staff is required by one of the following:

   • Physician report/letter
   • Operative report or other source documentation in the patient record (a laboratory report of azoospermia is required to document successful vasectomy)
   • Discharge summary
   • Laboratory report of azoospermia
   • FSH measurement elevated into the menopausal range as established by the reporting laboratory.
4. Ability and willingness of subject or legal guardian/representative to provide informed consent.

Exclusion Criteria:

1. Pregnancy or Breast-Feeding

2. Continuous use of the following medications for more than 3 days within 30 days of study entry:

   • Immunosuppressives
   • Immune modulators
   • Systemic glucocorticoids
   • Anti-neoplastic agents
3. Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
4. Serious illness requiring systemic treatment and/or hospitalization within 30 days prior to entry.
5. Surgery within the previous 3 months.
6. Any serious infectious, cardiac, pulmonary, or kidney disease
7. Hypersensitivity to Femarelle ®
8. Malignancy of the uterus or breast
9. Past thromboembolic event

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Collaborators and Investigators

• Sponsor: Hadassah Medical Organization

Study record dates

Study Major Dates

• Study Start: January 1, 2012

Study Registration Dates

• First Submitted: January 3, 2011
• First Submitted That Met QC Criteria: January 3, 2011
• First Posted (Estimate): January 4, 2011

Study Record Updates

• Last Update Posted (Estimate): August 28, 2012
• Last Update Submitted That Met QC Criteria: August 27, 2012
• Last Verified: August 1, 2011

More Information

Terms related to this study

• Other Study ID Numbers: 0172-10-HMO-CTIL