Medical Dissolution of Cholesterol Gallstones Using Oral Aramchol - A Proof of Concept Phase IIa Study

Gallstones Clinical Trial

Official title:

Medical Dissolution of Cholesterol Gallstones Using Oral Aramchol - A Proof of Concept Phase IIa Study

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02325492
• Other study ID #: Aramchol006
• Status: Terminated
• Phase: Phase 2
• First received: November 12, 2014
• Last updated: October 1, 2015
• Start date: October 2014
• Est. completion date: October 2015

Study information

• Verified date: December 2014
• Source: Galmed Pharmaceuticals Ltd
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

This is a one center, Phase IIa, randomized, double blind, placebo controlled study designed to evaluate the efficacy and safety of two Aramchol doses in subjects 18 to 75 years of age, with newly formed cholesterol gallstones in their gallbladder following bariatric surgery confirmed by gallbladder ultrasound ..

Description:

This is a one center, Phase IIa, randomized, double blind, placebo controlled study designed to evaluate the efficacy and safety of two Aramchol doses in subjects 18 to 75 years of age, with newly formed cholesterol gallstones in their gallbladder following bariatric surgery confirmed by gallbladder ultrasound performed in a period of 3 & 6 months following surgery before entering the study. All patients have ultrasonography evidence of clear gallbladder before the bariatric surgery.

Eligible subjects will be enrolled into three treatments arms: Aramchol 400 mg and 600 mg tablets and placebo tablets in ratio 1:1:1.

The subjects will be evaluated at study sites for 6 scheduled visits: at weeks -4 - 0 screening visit, Day 0 - baseline, weeks 2, 4, 8& 12 (Termination/early termination visit).

During the screening period the presence and number of cholesterol gallstones will be evaluated by gallbladder Ultrasound.

During the study the following assessments will be performed:

• Vital signs will be measured at each study visit.

• A physical examination will be performed at the screening visit, and termination/early termination visit.

• The following safety blood tests will be performed: complete blood count (CBC), serum chemistry (including electrolytes, liver enzymes, direct and total bilirubin, glucose, HbA1C, lipid profile which include cholesterol, HDL, LDL and VLDL, CPK, creatinine, urea, albumin, alkaline phosphatase), coagulation (fibrinogen, PT/INR, aPTT), ESR and urinalysis during the screening visit, baseline, week 2, 4, 8 and 12 (termination/early termination) visits. Serology (HBV, HCV and HIV) will be performed during the screening visit. β-hCG in women of child bearing potential will be performed during the screening visit.

• Body weight will be measured in screening, baseline and end of treatment visits. Height will be measured during the screening visit.

• ECG will be performed during the screening and end of treatment visits.

• Blood for Metabolomics will be collected at baseline and end of treatment visits.

• Ultrasound will be performed at screening visit, baseline, week 4, 8 and termination/early termination visits.

• Adverse events will be monitored throughout the study.

• Concomitant Medications will be monitored throughout the study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 10
• Est. completion date: October 2015
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Male or female age 18 to 75 years.

2. Presence of newly formed gallstones (size up to 6 mm) with or without sludge diagnosed by ultrasound within 3 or 6 months after bariatric surgery following normal ultrasound.

3. Bariatric surgery conducted during the last 12 months

4. Patients with "sleeve gastrectomy" or laparoscopic banding of the upper stomach will be included.

5. Signature of the written informed consent.

6. Negative pregnancy test at study entry for females of child bearing potential.

7. Females of child bearing potential practicing reliable contraception throughout the study period (not including oral contraceptives).

8. Hypertensive patients must be well 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).

9. Patients treated with vitamin E(>400IU/die), or Polyunsaturated fatty acid (>2g/d) or Ursodeoxycholic acid or fish oil can be included if drugs are stopped at least 3 months prior to study enrollment to the study and up to it end.

10. For patients with type 2 Diabetes, glycaemia must be controlled (Glycosylated Hemoglobin A1C = 8% while any HbA1C increment should not exceed 1% during 6 month prior to enrollment). If glycaemia is controlled by medications, qualitative change is not permitted within 3 months prior to randomization and should be avoided during the study. Treatments with Metformin, Sulfamides and Insulin are authorized. Sulfamides and insulin are permitted if glycaemia is self-monitored by the patient.

Exclusion Criteria:

1. Patients with ultrasonography evidence of gallstones in gallbladder before having the bariatric surgery.

2. Patients with no clear ultrasonography evidence of gallstones -free gallbladder during the year prior their bariatric surgery.

3. Patients with ultrasonography evidence of gallstones more than 1 year following bariatric surgery.

4. Patients with ultrasonography evidence of gallstones in size greater than 9 mm less than 1 year following bariatric surgery.

5. Weight >140 Kg or BMI >40

6. Known alcohol and/or any other drug abuse or dependence in the last five years

7. Known history or presence of clinically significant cardiovascular, hepatic, gastrointestinal, neurologic, pulmonary, endocrine, psychiatric, neoplastic disorder or nephritic syndrome.

8. History or presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs including bile salt metabolism (e.g. inflammatory bowel disease (IDB); previous intestinal (ileal or colonic) operation; chronic pancreatic; celiac disease or previous vagotomy

9. Uncontrolled blood pressure

10. Patients with HIV

11. Patients with renal dysfunction eGFR< 60.

12. Patients with pancreatitis, cholangitis or cholecystitis in the previous 4 months.

13. Women who are pregnant or breastfeeding

14. Type 1 Diabetes.

15. .Metformin, Fibrates, Statins, Insulin, Sulfonilurea not provided on a stable dose in the last 6 months.

16. Patients who are treated with Valproic acid, Tamoxifen, Methotreksate, Amiodaron.

17. Treatment with Rifaximin.

18. Homeopathic and/or Alternative treatments. Any treatment should be stopped before the screening period.

19. Serum creatine phosphokinase (CPK), ALT, AST and/or alkaline phosphatase >3X the upper limit of normal (ULN). Patients with an intermittent CPK elevation may have the repeated measurement prior to randomization; a CPK retest > 3X ULN leads to exclusion.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cholecystolithiasis
• Cholelithiasis
• Gallstones

Intervention

Drug:
• Aramchol

• Placebo

Device:
• Ultrasound

Locations

Country	Name	City	State
Israel	Assuta Medical Center	Tel Aviv

Sponsors (1)

Lead Sponsor	Collaborator
Galmed Pharmaceuticals Ltd

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Complete dissolution of existing gallstones proven by repeated US examined gallbladder	Change from baseline measured by US scan	At baseline and week 12	No
Secondary	Decrease of more than a 50% in number of stones. (change from baseline)	change from baseline measured by US scan	At baseline and week 12	No
Secondary	Prevention of formation of new gallstones during the study period	change from baseline measured by US scan	At baseline and week 12	No
Secondary	Dissolution of sludge.	change from baseline measured by US scan	At baseline and week 12	No