A Study to Evaluate the Effect of Mipomersen on Cardiac Repolarization Conducted in Healthy Subjects

Sponsor

Kastle Therapeutics, LLC (Industry)

Overall Status

Completed

CT.gov ID

NCT01090661

Collaborator

Ionis Pharmaceuticals, Inc. (Industry)

Enrollment

Location

Arms

Duration (Months)

29.9

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

To assess the electrocardiogram (ECG) effects of mipomersen administered as a 200-mg subcutaneous (SC) therapeutic and a 200-mg intravenous (IV; [2-hour infusion]) supra-therapeutic dose relative to placebo in healthy adult male and female subjects; and to evaluate the safety and pharmacokinetics (PK) of mipomersen when administered as a single therapeutic (200 mg) SC and a single, supra-therapeutic (200 mg) IV dose.

Condition or Disease	Intervention/Treatment	Phase
Healthy	Drug: mipomersen sodium Drug: mipomersen sodium Drug: moxifloxacin hydrochloride (Avelox®) Drug: placebo Drug: placebo	Phase 1

Detailed Description

This will be a randomized, double-blind, single-site, crossover study in healthy male and female subjects to determine if mipomersen administered as a single therapeutic (200 mg) SC and a single supra-therapeutic (200 mg) IV dose delays cardiac repolarization as determined by the measurement of QT/corrected QT (QTc) interval. A total of 60 healthy male and female subjects will be enrolled in this 4-way crossover study, randomly assigned to 1 of 8 treatment sequences, and cross over into 4 treatment periods where each subject will receive both a single SC injection and a single IV infusion during each period.

Study Design

Study Type:

Interventional

Actual Enrollment :

60 participants

Allocation:

Randomized

Intervention Model:

Crossover Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

A Randomized Double-Blinded Crossover Trial to Define the ECG Effects of Mipomersen (ISIS 301012) Using a Therapeutic and Supratherapeutic Dose Compared to Placebo and Moxifloxacin (a Positive Control) in Healthy Men and Women: A Thorough ECG Trial

Study Start Date :

Mar 1, 2010

Actual Primary Completion Date :

May 1, 2010

Actual Study Completion Date :

May 1, 2010

Arms and Interventions

Arm	Intervention/Treatment
Experimental: mipomersen IV (supra-therapeutic dose) 200 mg of mipomersen IV / placebo SC	Drug: mipomersen sodium 200 mg of mipomersen intravenous (IV) (single dose) Other Names: ISIS 301012 Drug: placebo placebo subcutaneous (SC) single dose
Experimental: mipomersen SC (therapeutic dose) 200 mg of mipomersen SC / placebo IV	Drug: mipomersen sodium 200 mg of mipomersen subcutaneous (SC) (single dose) Other Names: ISIS 301012 Drug: placebo placebo intravenous (IV) single dose
Active Comparator: moxifloxacin IV 400 mg of moxifloxacin IV / placebo SC	Drug: moxifloxacin hydrochloride (Avelox®) 400 mg of moxifloxacin intravenous (IV) single dose Drug: placebo placebo subcutaneous (SC) single dose
Placebo Comparator: placebo Placebo IV / placebo SC	Drug: placebo placebo intravenous (IV) single dose Drug: placebo placebo subcutaneous (SC) single dose

Outcome Measures

Primary Outcome Measures

change from baseline in QTcF (corrected Frederica's CT interval) [ECG monitoring up to 24 hours post dose]

Secondary Outcome Measures

ECG intervals (QTcB (corrected Bazett's QT interval), HR (heart rate, PR, QRS, and QT) [ECG monitoring up to 24 hours post dose]
change in ECG morphological patterns [ECG monitoring up to 24 hours post dose]
Correlation between delta delta QTc interval and plasma mipomersen concentrations [ECG monitoring up to 24 hours post dose]
Incidence of treatment-emergent Adverse Events [Assessed at each visit]
mipomersen plasma pharmacokinetic (PK) parameters: Area Under the Curve (AUC 0-22.5h), Maximum Concentration (Cmax), Time to Maximum Concentration (Tmax) [Serial PK sampling up to 24 hours post dose]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 45 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Written informed consent provided before any study-related procedures are performed.
Body mass index (BMI) of 19 to 32 kg/m2 inclusive.
Subjects can not have consumed nicotine or nicotine-containing products for at least 6 months before Screening.
Subjects are nonpregnant and nonlactating, surgically sterile, postmenopausal, abstinent, or subject or partner is willing to use a reliable method of contraception during the study and 5 months after the last dose of investigational product.

Exclusion Criteria:

History of risk factors for Torsades de Pointes, known Long QT Syndrome, heart failure, myocardial infarction, angina, or clinically significant abnormal laboratory assessments or family history of Long QT or Brugada Syndrome.
Abnormal screening ECG that is interpreted by the Investigator to be clinically significant.
Use of concomitant medications (prescribed or over-the-counter), without the approval of the Investigator and Sponsor, within 7 days before the first dose of investigational product.
Clinically significant abnormal findings on the physical examination, ECG, blood pressure, heart rate, medical history, or clinical laboratory results at Screening or before dosing.
History of clinically significant allergies or hematological, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease.
Positive test for HIV antibody, hepatitis C antibody, or hepatitis B surface antigen.
Positive test for drugs of abuse, alcohol, or cotinine at Screening or before dosing or history of drug or alcohol abuse or dependence within 1 year before Screening.
History of cancer, with the exception of basal cell carcinoma.