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Clinical Trials/NCT00805805
NCT00805805
Completed
Phase 3

Phase III Trial of Tetrathiomolybdate (TM) in Primary Biliary Cirrhosis

George Brewer1 site in 1 country29 target enrollmentApril 2006

Overview

Phase
Phase 3
Intervention
Tetrathiomolybdate
Conditions
Primary Biliary Cirrhosis
Sponsor
George Brewer
Enrollment
29
Locations
1
Primary Endpoint
Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The University of Michigan is conducting a study investigating a potential new treatment aimed at slowing/halting progression of primary biliary cirrhosis. This will be a 2 arm double blind study in which half of the patients will be randomly selected to receive a placebo (capsule with no active ingredient) and half will receive the new treatment drug, tetrathiomolybdate. Neither the patient nor the treating physician will know which arm the patient is in. The length of the study for each patient is 24 months of drug therapy. Lab draws will be necessary weekly for the first 6 weeks of the study, followed by every other week for 3 weeks, and then monthly for the remainder of the 2 year period. In addition, intermittent history and physicals and urine samples will also be necessary. There is no cost to you for any experimental treatment. All patients in both arms will continue on ursodiol and receive standard of care treatment

Registry
clinicaltrials.gov
Start Date
April 2006
End Date
December 2008
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

George Brewer

Professor

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Generally medically healthy
  • Age 18 and older
  • Documented primary biliary cirrhosis
  • Alkaline phosphatase \> 137

Exclusion Criteria

  • Severe liver decompensation
  • Requirement for renal dialysis
  • Pregnancy or nursing
  • Meld score \> 15 (13-15 will require a physician's clinical judgment)
  • Uncontrolled congestive heart failure
  • Severe diabetic neuropathy
  • Severe pulmonary disease
  • Advanced cancer
  • Requirement for steroid therapy
  • Uncontrolled ascites, variceal hemorrhage or spontaneous bacterial peritonitis

Arms & Interventions

1

Tetrathiomolybdate with ursodiol

Intervention: Tetrathiomolybdate

2

Placebo with ursodiol

Intervention: Placebo

Outcomes

Primary Outcomes

Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement

Time Frame: 2 years

Secondary Outcomes

  • Improvement in drug treated group vs placebo group in serum CRP or interleukin-1-beta-levels(2 years)

Study Sites (1)

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