Study to Investigate the Effect of GSK1014802 on Ambulatory Blood Pressure

NCT ID: NCT00955396

Last Updated: 2017-10-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2009-12-31

Brief Summary

In this study the investigators will determine whether there is any effect of GSK1014802 on ambulatory blood pressure. This will be a randomized, double-blind, placebo-controlled, repeat dose, 2 period cross-over study conducted in healthy male and female subjects. Approximately 60 subjects will be randomised to receive GSK1014802 400 mg bid and placebo for 36 days with at least 1 week between treatment sessions. A follow-up will occur 7-14 days after the last dose.

Detailed Description

This study, previously posted by GlaxoSmithKline (GSK), was transitioned to Convergence Pharmaceuticals, Ltd., which spun off from GSK. Convergence Pharmaceuticals, Ltd., has now been acquired by Biogen.

Conditions

Healthy Volunteer

Keywords

sodium channel blocker; ambulatory blood pressure

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

Period 1

Group Type: OTHER

GSK1014802

Intervention Type: DRUG

Tablets

Placebo

Intervention Type: DRUG

Tablets

Period 2

Group Type: OTHER

GSK1014802

Intervention Type: DRUG

Tablets

Placebo

Intervention Type: DRUG

Tablets

Interventions

GSK1014802

Tablets

Intervention Type: DRUG

Placebo

Tablets

Intervention Type: DRUG

Other Intervention Names

BIIB074 and CNV1014802

Eligibility Criteria

Inclusion Criteria

• Male or female between 18 and 65 years of age inclusive.
• Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests, liver function and cardiac monitoring.
• A female subject is eligible to participate if she is of:

Non-childbearing potential Child-bearing potential and agrees to use a contraception method.

• Male subjects must agree to use a contraception methods
• Body weight ≥ 50 kg and BMI within the range 19 - 40.0 kg/m2 (inclusive).
• Arm circumference ≥ 24 and ≤ 42 cm at mid level.
• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion Criteria

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
• Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
• A positive pre-study drug screen.
• Alcohol levels above the legal limit for driving at screening and the detection of any alcohol within 24 h prior to the start of dosing in Treatment Periods 1 and 2.
• A positive test for HIV antibody.
• History of regular excessive alcohol consumption within 6 months of the study
• The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
• Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
• Use of prescription or non-prescription drugs, including any antihypertensive agent including diuretics, vitamins, herbal and dietary supplements
• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy
• Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 90 day period.
• Pregnant females as determined by positive serum or urine hCG test at screening or prior to dosing.
• Lactating females.
• Unwillingness or inability to follow the procedures outlined in the protocol.
• Subject is mentally or legally incapacitated.
• Subjects who work at night or whose work schedule includes rotating night time (10:00 PM to 6:00 AM) work.
• Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.
• Average daily caffeine intake equivalent to > 4 cups of coffee or > 6 cups of tea.
• Consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices from 7 days prior to the first dose of study medication.
• Consumption of aged cheeses and meats, soy sauce and other tyramine rich sources within 1 day prior to the baseline assessments.
• Current or past history of symptomatic orthostatic hypotension or history of unexplained vasovagal episode(s).
• History of known or suspected seizures, including infantile febrile, unexplained significant and recent loss of consciousness or history of significant head trauma with loss of consciousness or a family history (first degree relative) of epilepsy or seizures (fits).
• Any history of suicidal behaviour or suicidal ideation of type 4 or 5 on the C-SSRS within 3 months of the screening visit.
• History or currently diagnosed sleep apnea.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Biogen

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Biogen Medical Director

Role: STUDY_DIRECTOR

Biogen

Locations

GSK Investigational Site

Buffalo, New York, United States

Countries

United States

Other Identifiers

SCB113210

Identifier Type: -

Identifier Source: secondary_id

113210

Identifier Type: -

Identifier Source: org_study_id