Safety, Tolerability and Pharmacokinetics of Repeat Doses of GSK1014802.

NCT ID: NCT00908154

Last Updated: 2017-10-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 51 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-05-31
• Study Completion Date: 2008-12-31

Brief Summary

GSK1014802 is a use-dependent sodium channel blocker and an effective anticonvulsant in animal models.

This study is being conducted to obtain information regarding the safety, tolerability and pharmacokinetics of repeated doses of GSK1014802 administered for up to 28 days in healthy male or female subjects. In addition, the effect of food on the pharmacokinetics of GSK1014802 will be investigated.

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

Bipolar Depression; Bipolar Disorder

Keywords

sodium channel blocker; bipolar disorder; repeat dose

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Cohort 1

Group Type: OTHER

Placebo

Intervention Type: DRUG

Tablets to match GSK1014802

GSK1014802

Intervention Type: DRUG

Sodium channel blocker

Cohort 4

Group Type: OTHER

Placebo

Intervention Type: DRUG

Tablets to match GSK1014802

GSK1014802

Intervention Type: DRUG

Sodium channel blocker

Cohort 3

Group Type: OTHER

Placebo

Intervention Type: DRUG

Tablets to match GSK1014802

GSK1014802

Intervention Type: DRUG

Sodium channel blocker

Cohort 2

Group Type: OTHER

Placebo

Intervention Type: DRUG

Tablets to match GSK1014802

GSK1014802

Intervention Type: DRUG

Sodium channel blocker

Interventions

Placebo

Tablets to match GSK1014802

Intervention Type: DRUG

GSK1014802

Sodium channel blocker

Intervention Type: DRUG

Other Intervention Names

BIIB074 and CNV1014802

Eligibility Criteria

Inclusion Criteria

• Healthy as determined by a responsible physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring.

• Male or female (of non-child bearing potential) subjects aged between 18 and 55 years.
• A female subject is eligible to participate if she is of non-childbearing potential.
• Male subjects must agree to use an acceptable form of contraception.
• Body weight ≥ 50 kg and BMI within the range 19 - 29.9 kg/m2 (inclusive)
• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
• QTcB or QTcF < 450 msec; or QTc < 480 msec in subjects with Bundle Branch Block.

Exclusion Criteria

• The subject has a positive pre-study drug/alcohol screen.

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
• A positive test for HIV antibody.
• History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units (males), or defined as an average weekly intake of greater than 14 units or an average daily intake of greater than 2 units (females).
• Current or past history of symptomatic orthostatic hypotension or history of unexplained vasovagal episode(s).
• 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 (60 h) 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 vitamins, herbal and dietary supplements (including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication.
• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
• Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
• Pregnant females.
• Lactating females.
• Unwillingness or inability to follow the procedures outlined in the protocol.
• History of sensitivity to heparin or heparin-induced thrombocytopenia.
• Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.
• . 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.
• 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).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 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

London, , United Kingdom

Countries

United Kingdom

Other Identifiers

SCB107727

Identifier Type: -

Identifier Source: secondary_id

107727

Identifier Type: -

Identifier Source: org_study_id