Thorough QT/QTc (Corrected QT Interval) Study to Evaluate the Effect of Custirsen on Cardiac Repolarization

NCT ID: NCT01874561

Last Updated: 2016-10-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 155 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-05-31
• Study Completion Date: 2014-01-31

Brief Summary

This is a 3-arm, parallel-group, active- and placebo-controlled, double-blind, randomized study, to compare treatment with intravenous custirsen at 640 mg (highest intended therapeutic dose) with placebo. The purpose of this study is to assess the effect of custirsen treatment on cardiac conduction and repolarization (electrical activity of the heart) in healthy subjects. The positive control employed to demonstrate assay sensitivity consists of a group receiving a single oral dose of 400 mg moxifloxacin on day 7. The moxifloxacin arm is un-blinded but the ECG readings are blinded.

Detailed Description

The effects of custirsen will be evaluated following administration of a single dose following dose-titration period combined with dexamethasone pretreatment. On days -1 and 7, subjects will undergo a full ECG assessment for 24 hours. On day 1, randomization and assignment to the treatment groups will be performed prior to drug administration. Subjects will remain in the study center throughout the treatment period. All subjects will be discharged at the end of day 8 procedures, 24 hours after the last dose of custirsen has been administered. Subjects in groups 1 and 2 will return for an additional visit on day 9, 10 and 14 (±2 days) (approximately 7 days after the last study drug administration). Subjects in group 3 will not return for a follow-up visits.

Conditions

Cardiac Conduction and Repolarization

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Group 1

Group 1: investigational product (custirsen) will receive:

• 320 mg of custirsen + 5 mg of dexamethasone on day 1
• 480 mg of custirsen + 5 mg of dexamethasone on day 3
• 640 mg of custirsen + 3 mg of dexamethasone on day 5
• 640 mg of custirsen on day 7 under fasting conditions

Group Type: EXPERIMENTAL

Custirsen

Intervention Type: DRUG

Custirsen will be administered iv using an infusion pump over a 2-hour period.

Group 2

Group 2: placebo (normal saline) will receive:

• placebo + 5 mg of dexamethasone on day 1
• placebo + 5 mg of dexamethasone on day 3
• placebo + 3 mg of dexamethasone on day 5
• placebo on day 7 under fasting conditions

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo (commercially available normal saline) will be administered iv using an infusion pump over a 2-hour period.

Group 3

Group 3: positive control (moxifloxacin) will receive:

• placebo + 5 mg of dexamethasone on day 1
• placebo + 5 mg of dexamethasone on day 3
• placebo + 3 mg of dexamethasone on day 5
• 400 mg of moxifloxacin + placebo (immediately after moxifloxacin administration) on day 7 under fasting conditions

Group Type: ACTIVE_COMPARATOR

Moxifloxacin

Intervention Type: DRUG

Moxifloxacin (400 mg) will be administered orally with 240 mL of room temperature still water.

Interventions

Custirsen

Custirsen will be administered iv using an infusion pump over a 2-hour period.

Intervention Type: DRUG

Placebo

Placebo (commercially available normal saline) will be administered iv using an infusion pump over a 2-hour period.

Intervention Type: DRUG

Moxifloxacin

Moxifloxacin (400 mg) will be administered orally with 240 mL of room temperature still water.

Intervention Type: DRUG

Other Intervention Names

custirsen sodium; Normal saline

Eligibility Criteria

Inclusion Criteria

1. The subject is a man aged 18 through 45 years of age with a body mass index (BMI) of 18 through 30 kg/m2 at screening.

2. The subject is in good health as determined by medical history, ECG, vital signs measurements, physical examination, and clinical laboratory tests.

3. The subject must be able to understand and comply with the requirements of the study (eg, all medication, dietary, exercise, tobacco, and alcohol restrictions).

4. The subject must provide written informed consent to participate in the study after reading the information and consent form, and after having an opportunity to discuss the study with the investigator or delegate.

Exclusion Criteria

• The subject has an ECG abnormality that may interfere with the accurate assessment of the QT interval, including intraventricular conduction delays (QRS >120 msec or PR >200 as measured at the screening and check-in visits) and complete or incomplete bundle branch blocks.
• The subject has a resting QTcF interval of ≤360 msec and/or ≥450 msec measured at screening or day -2.

• The subject has a known clinically significant (in the opinion of the investigator) cardiovascular disorder, including coronary artery disease, valvular heart disease, cardiomyopathies, or an ECG abnormality suggestive of prior myocardial infarction, angina pectoris, chamber enlargement, or hypertrophy. Notwithstanding, subjects with known significant disorders will be excluded.
• The subject has a known clinically significant arrhythmia or rhythm disturbance observed on the screening and/or day -2 12-lead ECG.
• The subject has a supine pulse rate outside of the range of 40 to 100 bpm (following at least a 10-minute rest) measured at screening or day -2.
• The subject has a supine blood pressure outside of the range of 90 to 139 mm Hg systolic or 50 to 89 mm Hg diastolic (following at least a 10-minute rest) measured at screening and on day -2. Note: The blood pressure measurement may be repeated up to 3 times to meet eligibility requirements. In this case, the average of these 3 measurements must meet eligibility criteria.
• The subject reports a history of, or risk factors for, Torsades de Pointes (eg, congestive heart failure, serum electrolyte abnormalities) including a family history of arrhythmia, sudden unexplained death at a young age (before 40 years) in a first-degree relative, or long QT syndrome, or a personal history of syncope.

3. The subject has low serum potassium and/or magnesium and/or corrected calcium blood levels (less than 3.5 milliequivalent/liter (mEq/L), 1.8 mEq/L, and 8.9 mg/dL, respectively) at screening and/or day-2.

4. The subject has any condition that may possibly interfere with drug absorption, distribution, metabolism, or excretion (eg, previous surgery on the gastrointestinal tract [including removal of parts of stomach, bowel, liver, gall bladder, or pancreas] or stomach banding).

5. The subject has an abnormality in medical history, physical examination, biochemistry, hematology, coagulation, serology, or urinalysis at the screening or admission visit that is considered clinically significant by the investigator or meets grades 2-4 Common Terminology Criteria for Adverse Events (CTCAE) v.4 criteria, or in the opinion of the investigator, could interfere with the objective of the study or the safety of the subject. Notwithstanding, the following values must remain within the normal range values (as determined by the Physician Reference Laboratory [PRL]) in order for a subject to be eligible for the study: calcium, magnesium, potassium, creatinine, ALT, AST, GGT, hemoglobin, absolute lymphocyte count, absolute 50 mg/dL in asymptomatic subjects and absolute leukocyte count values as low as 3.1x109/L in African American subjects will be considered for enrollment at the investigator's discretion. Lastly, the upper limit value for exclusion is modified for the following values and is as follows: INR>1.2, total bilirubin>1.2 mg/dL, serum amylase >143 U/L, LDH>261 U/L, and CPK>367 U/L, which do not normalize upon repeat testing, will be exclusionary.

6. The subject has used one of the prohibited drugs, substances or foods as follows:

• any investigational product within 60 days (or 5 half-lives, whichever is longer) preceding the study
• any prescription or nonprescription medication (including herbal remedies, vitamins, or dietary supplements) or vaccine within 14 days of the first day of study drug administration (day 1) or within 5 half-lives before the first day of study drug administration, whichever is longer. Exceptions are locally acting medications (eg, topical creams), which are not allowed within 5 days of study drug administration, and the occasional use of acetaminophen (up to 3 g/day) and ibuprofen (up to 1200 mg/day).
• consumption of grapefruit, grapefruit juice, Seville oranges, pomelo-containing products, within the 14 days prior to day -1 and then throughout the entire study
• consumption of excessive amounts of alcoholic beverages, defined as more than 3 drinks per day (beer, wine, or distilled spirits), or unwillingness to comply with the restricted use of alcohol during the study (96 hours prior to admission and until 48 hours after the last study drug administration), history of alcoholism, or evidence of drug/chemical abuse
• positive urine drug (cocaine, amphetamines, barbiturates, opiates, phencyclidine, benzodiazepines, tetrahydrocannabinol), cotinine, or alcohol screen at the screening visit or admission
• consumption of quinine (eg, tonic water) within 7 days prior to admission

7. The subject has any other condition, which, in the opinion of the investigator, makes the subject inappropriate for the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Teva Branded Pharmaceutical Products R&D, Inc.

INDUSTRY

Sponsor Role: collaborator

Achieve Life Sciences

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Teva Investigational Site 10565

Lenexa, Kansas, United States

Countries

United States

Other Identifiers

TV1011-TQT-108

Identifier Type: -

Identifier Source: org_study_id