Efficacy and Safety of Gemcabene in Patients With Homozygous Familial Hypercholesterolemia on Stable, Lipid-Lowering Therapy (COBALT-1)

NCT02722408 | Completed Phase 2 Results

• 1 other identifier: GEM-201
• Study Type: interventional
• Target: 8
• Locations: 3 countries
• Sites: 7

Brief Summary

The purpose of this study was to assess the efficacy, safety, and tolerability of multiple doses of Gemcabene in patients with HoFH on stable, lipid-lowering therapy.

Conditions

Hypercholesteremia

Keywords

LDL-C; Lipid Regulator

Outcome Measures

Primary Outcomes (3)

• Percent Change From Baseline in LDL-C at Day 28

  Baseline, day 28

• Percent Change From Baseline in LDL-C at Day 56

  Baseline, day 56

• Percent Change From Baseline in LDL-C at Day 84

  Baseline, day 84

Secondary Outcomes (46)

• Change From Baseline in Fasting LDL-C

  Baseline, days 28, 56 and 84

• Percent Change From Baseline in Fasting Non-HDL-C

  Baseline, days 28, 56 and 84

• Change From Baseline in Fasting Non-HDL-C

  Baseline, days 28, 56 and 84

• Percent Change From Baseline in Fasting Total Cholesterol (TC)

  Baseline, days 28, 56 and 84

• Change From Baseline in Fasting Total Cholesterol (TC)

  Baseline, days 28, 56 and 84

Study Arms (1)

Gemcabene

EXPERIMENTAL

Participants with homozygous familial hypercholesterolemia (HoFH) on stable lipid lowering therapy received 300 milligram (mg) of Gemcabene, orally once daily from day 1 to 28 followed by 600 mg of Gemcabene, orally once daily from day 29 to 56 followed by 900 mg of Gemcabene, orally once daily from day 57 to 84. Participants were followed until Day 112.

Drug: Gemcabene

Interventions

Gemcabene DRUG

300 mg tablet orally once daily for four weeks followed by 600 mg tablet orally once daily for four weeks followed by 900 mg tablet orally once daily for four weeks.

Gemcabene

Eligibility Criteria

• Age: 17 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Provision of written and signed informed consent (by patient or legal guardian) prior to any study-specific procedure;
• Male or female ≥17 years of age at time of consent;
• Diagnosis of HoFH by genetic confirmation (including compound heterozygosity) or a clinical diagnosis based on either (1) a history of an untreated LDL-C concentration \>500 mg/dL (12.92 mmol/L) together with either appearance of xanthoma before 10 years of age, or evidence of heterozygous familial hypercholesterolemia in both parents or, if history is unavailable, (2) LDL-C \>300 mg/dL (7.76 mmol/L) on maximally tolerated lipid-lowering drug therapy;
• Currently on a stable, low-fat, low-cholesterol diet in combination with a pre-existing, regulatory-approved, not excluded lipid-lowering therapy (i.e., statins, monoclonal antibodies to PCSK9, cholesterol absorption inhibitors, bile acid sequestrants, or nicotinic acid, or any combination thereof) at a stable dose for at least 4 weeks prior to the Screening Visit;
• Fasting LDL-C value \>130 mg/dL (3.36 mmol/L) at the Screening Visit;
• Physical examination, including vital signs, that is within normal limits or clinically acceptable to the Investigator;
• Weight ≥50 kg;
• Female patients must not be pregnant or lactating. Women of child-bearing potential must have a negative serum pregnancy test at the Screening Visit and negative urine dipstick on Day 1 prior to dosing in order to qualify for the study. Women who are surgically sterile or are clinically confirmed to be post-menopausal (i.e., documented amenorrhea for ≥1 year in the absence of other biological or physiological causes) are not considered to be of child-bearing potential; and
• Women of child-bearing potential must agree to use acceptable methods of contraception throughout the duration of the study and for 30 days after the last dose of study drug. For this study, double-barrier contraception is required.

You may not qualify if:

• Other forms of primary hyperlipoproteinemia and secondary causes of hypercholesterolemia (e.g., nephrotic syndrome or hypothyroidism);
• Abnormal liver function test at the Screening Visit (aspartate aminotransferase or alanine aminotransferase \>2 × the upper limit of normal \[ULN\]; total bilirubin \>1.5 × ULN; or alkaline phosphatase \>2 × ULN based on appropriate age and gender normal values). Patients with bilirubin \>1.5 × ULN and history of Gilbert's syndrome may be included; reflexive direct bilirubin testing will be used to confirm Gilbert's syndrome;
• Moderate (Grade B) or severe (Grade C) chronic hepatic impairment according to the Child Pugh classification;
• Active liver disease (e.g., cirrhosis, alcoholic liver disease, hepatitis B virus \[HBV\], hepatitis C virus \[HCV\], autoimmune hepatitis, liver failure, liver cancer), history of liver transplant, or known diagnosis of human immunodeficiency virus (HIV);
• Triglycerides value \>400 mg/dL (4.52 mmol/L) at the Screening Visit;
• Moderate to severe renal insufficiency defined as an estimated GFR \<30 mL/min/1.73m2 (calculated using The Chronic Kidney Disease Epidemiology Collaboration equation) at the Screening Visit;
• Abnormal urinalysis (proteinuria greater than trace or any male or non-menstruating female with greater than trace hematuria), confirmed by reflexive urine protein:creatinine ratio testing;
• Uncontrolled thyroid disease: hyperthyroidism or hypothyroidism as defined by thyroid stimulating hormone (TSH) below the lower limit of normal or \>1.5 × ULN, respectively, at the Screening Visit. If controlled, treatment should be stable for at least 3 months prior to the Screening Visit;
• Type 1 diabetes mellitus or uncontrolled type 2 diabetes mellitus (hemoglobin A1c \[HbA1c\] value \>8%), or any diabetic patient taking insulin and/or thiazolidinediones;
• New York Heart Association Class III or IV heart failure;
• Myocardial infarction, severe or unstable angina pectoris, coronary angioplasty, coronary artery bypass graft, or other major cardiovascular events resulting in hospitalization within 3 months of the Screening Visit. Patients with adequately treated stable angina, per Investigator assessment, may be included;
• Uncontrolled cardiac arrhythmia or prolonged QT on the Screening Visit or Day 1 prior to dosing ECG (QTcF \>450 msec for men and \>470 msec for women) or known family history of prolonged QT or unexplained sudden cardiac death;
• Uncontrolled hypertension, defined as sitting systolic blood pressure \>180 mmHg or diastolic blood pressure \>110 mmHg, and confirmed by repeat measurement;
• Currently receiving cancer treatments or, in the Investigator's opinion, at risk of relapse for recent cancer;
• Use of fibrate lipid-lowering agent 6 weeks prior to the Screening Visit;

Sponsors & Collaborators

• NeuroBo Pharmaceuticals Inc.: lead

Study Sites (7)

Westside Medical Associates of Los Angeles

Beverly Hills, California, United States

Location

Robarts Research Institute

London, Ontario, Canada

Location

Ecogene-21

Chicoutimi, Quebec, Canada

Location

Montreal Heart Institute

Montreal, Quebec, Canada

Location

Wolfson Medical Center Internal Medicine Dept.

Holon, Israel

Location

Center for Research, Prevention and Treatment of Atherosclerosis - Cardiology Department of Medicine Kiryat Hadassah

Jerusalem, Israel

Location

Ziv Medical Center Internal Medicine Department

Safed, Israel

Location

Related Publications (1)

• Gaudet D, Durst R, Lepor N, Bakker-Arkema R, Bisgaier C, Masson L, Golden L, Kastelein JJ, Hegele RA, Stein E. Usefulness of Gemcabene in Homozygous Familial Hypercholesterolemia (from COBALT-1). Am J Cardiol. 2019 Dec 15;124(12):1876-1880. doi: 10.1016/j.amjcard.2019.09.010. Epub 2019 Sep 26.

  PMID: 31685212 DERIVED

MeSH Terms

Conditions

Hypercholesterolemia

Interventions

gemcabene

Condition Hierarchy (Ancestors)

Hyperlipidemias; Dyslipidemias; Lipid Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases

Results Point of Contact

• Title: Vice President Clinical Operations
• Organization: NeuroBo Pharmaceuticals

info@neurobopharma.com

+1 (857) 702-9600

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 12, 2016
• First Posted: March 30, 2016
• Study Start: June 1, 2016
• Primary Completion: April 1, 2017
• Study Completion: July 1, 2017
• Last Updated: June 25, 2020
• Results First Posted: June 25, 2020

Record last verified: 2020-06

Locations

CA (3); IL (3); US (1)