Study of the Effect of GS-6615 in Subjects With LQT-3

NCT ID: NCT01849003

Last Updated: 2014-11-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-05-31
• Study Completion Date: 2014-11-30

Brief Summary

This mechanism of action study is to evaluate the effect of oral GS-6615 on the QTc interval in participants with Long QT-3 syndrome. This study will be performed in six cohorts of participants in a sequential manner, four single-dose cohorts followed by two multiple-dose cohorts. Duration of treatment for the single-dose cohorts and multiple-dose cohorts will be 1 day and 7 days, respectively. Participants will be confined at the study center from check-in until completion of assessments at discharge.

Participants will be continuously monitored using real-time telemetry throughout the in-clinic confinement. Physical examinations including vital signs, laboratory analysis, electrocardiograms (ECGs), Holter recordings and echocardiography (ECHO) will be performed at defined time points throughout the study period. Assessment of adverse events and concomitant medications will continue throughout the duration of the study.

Conditions

Long QT Syndrome

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 1

Participants will receive a single 10 mg dose of GS-6615.

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Cohort 2

Participants will receive a single 20 mg dose of GS-6615.

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Cohort 3

Participants will receive a single 30 mg dose of GS-6615.

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Cohort 4

Participants will receive a single 60 mg dose of GS-6615.

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Cohort 5

Participants will receive single doses of GS-6615 as follows:

• Day 1: 20 mg (loading dose)
• Day 2: 40 mg (loading dose)
• Days 3-7: 6 mg (maintenance dose) once daily

If a participant has a QTcF value of ≤ 420 msec on 2 consecutive time points after the 20 mg dose on Day 1, the participant will receive the maintenance dose of 6 mg on Day 2.

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Cohort 6

Participants will receive single doses of GS-6615 as follows:

• Day 1: 50 mg (loading dose)
• Day 2-3: 10 mg once daily
• Days 4-7: 20 mg once daily

Group Type: EXPERIMENTAL

GS-6615

Intervention Type: DRUG

GS-6615 tablet(s) administered orally

Interventions

GS-6615

GS-6615 tablet(s) administered orally

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Males and females between ages 18-65 years (inclusive) at time of screening

2. Documented LQT-3 genotype with one of the following mutations: delta KPQ, R1623Q, N1325S, E1784K, S1787N, D1790G, G1631D, 1795insD, delF1617, R1644H, L409P, F2004L, I1768V, T1304M, A1330T, or F1596I3.

3. QTc > 480 msec in lead V5 at screening

4. Weight of at least 50 kg with body mass index (BMI) between 18 and 30 kg/m^2 (inclusive)

5. Females of childbearing potential must have a negative serum pregnancy test at screening and check-in

6. Females of childbearing potential must agree to utilize protocol recommended highly effective contraception methods from three weeks prior to the single dose of study drug and for 30 days following the single dose of study drug

a. Females who utilize hormonal contraceptive as one of their birth control methods must have used the same method for at least 3 months prior to study dosing

7. Males must agree to utilize a protocol recommended highly effective method of contraception during heterosexual intercourse throughout the study period and for 90 days following last dose of study drug. Periodic abstinence and withdrawal are not acceptable methods of contraception

8. Males must refrain from sperm donation from Day -2 through completion of the study and continuing for at least 90 days from the date of last dose of study drug

9. Willing and able to comply with the requirements of the protocol and directions from the clinic staff

10. Willing to avoid consumption of grapefruit, grapefruit juice and Seville oranges within 2 weeks prior to the single dose of study drug until discharge from the clinic

11. Willing to avoid consumption of nicotine (including nicotine gum) and alcoholic beverages within 2 weeks prior to the single dose of study drug until discharge from the clinic

12. Understand and willing to sign informed consent

Exclusion Criteria

1. Ongoing or history of any medical or surgical condition that, in the judgment of the Investigator, might jeopardize the individual's safety or interfere with the absorption, distribution, metabolism or excretion of the study drug

2. History of meningitis or encephalitis, seizures, migraines, tremors, myoclonic jerks, sleep disorder, anxiety, syncope, head injuries or a family history of seizures

3. Any abnormal electrocardiographic (ECG) findings (except QTc > 460 msec) at screening judged to be clinically significant by the investigator

4. Any abnormal laboratory value or physical examination finding at screening or check-in that is judged by the investigator as clinically significant

5. History of positive serology test for HIV, or hepatitis B or C

6. Positive urine drug test for ethanol, barbiturates, cocaine, opiates, or amphetamines at screening or check-in

7. Positive urine cotinine test at check-in

8. Current treatment with drugs affecting the QT interval

9. Current treatment with sodium-channel blockers, eg, flecainide and mexiletine

10. Current treatment with strong or moderate inhibitors or inducers of cytochrome P450 (CYP)3A4 and 1A2

11. Prior treatment with ranolazine within 7 days prior to study drug administration

12. Use of systemic prescription medications or over-the-counter (OTC) medication, including multivitamins, and dietary and herbal supplement within 2 weeks or 5 times the terminal half-lives of the medication (whichever is longer) prior to the single dose of study drug, and for the duration of the study

13. Use of any experimental or investigational drug or device within 30 days prior to the single dose of study drug or 5 half-lives of the drug, whichever is longer

14. Females who are pregnant or lactating

15. History of drug or alcohol abuse within 12 months prior to initial dosing of study drug

16. Psychosocial or addictive disorders that would interfere with ability to give informed consent or could compromise compliance with the protocol

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Gilead Sciences

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Elizabeth Layug, MD

Role: STUDY_DIRECTOR

Gilead Sciences

Locations

University of Rochester Medical Center/Strong Memorial Hospital

Rochester, New York, United States

Countries

United States

Other Identifiers

GS-US-279-0110

Identifier Type: -

Identifier Source: org_study_id