Study to Evaluate the Effects of MBX-8025 in Patients With HoFH

PHASE2CompletedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

April 30, 2015

Primary Completion Date

February 29, 2016

Study Completion Date

February 29, 2016

Conditions
Homozygous Familial Hypercholesterolemia
Interventions
OTHER

Run-In Period: Placebo

2 capsules, once a day for two weeks

DRUG

MBX-8025 50 mg (Dose Escalation Period 1)

"1 capsule once a day for 4 weeks~(MBX-8025 50 mg capsule)"

DRUG

MBX-8025 50 mg or 100 mg (Dose Escalation Period 2)

"1 capsule once a day for 4 weeks~(MBX-8025 50 mg or 100 mg capsule)"

DRUG

MBX-8025 50 mg, 100 mg or 200 mg (Dose Escalation Period 3)

"1 or 2 capsules once a day for 4 weeks~(MBX-8025 50 mg, 100 mg or two (2) 100 mg capsules)"

Trial Locations (5)

G7H 7K9

Ecogene-21, Chicoutimi

H1T 1C8

Montreal Heart Institute, Montreal

75 013

Endocrinologie metabolisme et prevention cardiovasulaire, Institut E3M et IHU cardiometabolique (ICAN), Hôpital Pitié Salpêtrière, Paris

6525 GA

Radbound UMC, Nijmegen

N-0373

Lipidklinikken, Oslo Universitetssykehus, Oslo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY