Status:

COMPLETED

Effect of CER-001 on Plaque Volume in Homozygous Familial Hypercholesterolemia (HoFH) Subjects

Lead Sponsor:

Cerenis Therapeutics, SA

Conditions:

Homozygous Familial Hypercholesterolemia

Eligibility:

All Genders

12+ years

Phase:

PHASE2

Brief Summary

The available medications used to treat HoFH are targeted at reducing circulating levels of total and LDL-cholesterol. These measures can retard the progression of cardiovascular disease, however, the...

Eligibility Criteria

Inclusion

  • Male or female subject 12 years or older
  • Subject presents with Homozygous FH

Exclusion

  • Weight \>100 kg
  • Subjects with significant health problems in the recent past including blood disorders, cancer, or digestive problems
  • Female subjects of child-bearing potential
  • Known major hematologic, renal , hepatic, metabolic, gastrointestinal or endocrine dysfunction
  • Contraindication to MRI scanning that would preclude the use of contrast-enhanced 3TMRI

Key Trial Info

Start Date :

November 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2014

Estimated Enrollment :

23 Patients enrolled

Trial Details

Trial ID

NCT01412034

Start Date

November 1 2011

End Date

August 1 2014

Last Update

August 18 2015

Active Locations (9)

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Page 1 of 3 (9 locations)

1

Clinical Research Facility

Hartford, Connecticut, United States, 06102

2

Clinical Research Facility

North Massapequa, New York, United States, 11758

3

Clinical Research Facility

Chicoutimi, Quebec, Canada, G7H 7P2

4

Clinical Research Facility

Québec, Quebec, Canada, G1V4M6