Use Of GW274150 In The Prophylactic Treatment Of Migraine

Study Description

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Brief Summary:

Nitric oxide (NO) is likely to be involved in the development of migraine headache. Nitric oxide synthase (NOS) is an important chemical involved in the production of NO. Reduction of NOS, and therefore NO, may be an effective technique for the prevention of migraine headache. GW274150 is a highly selective inhibitor of NOS and offers the potential of anti-inflammatory activity in migraine through a novel mechanism of action. The intent of this study is to investigate the safety and efficacy of GW274150 for the prophylactic treatment of migraine headache.

Condition or disease	Intervention/treatment	Phase
Migraine Disorders	Drug: GW274150; Other: Placebo	Phase 2

Study Design

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Study Type :	Interventional (Clinical Trial)
Actual Enrollment :	430 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Masking:	Double (Participant, Investigator)
Primary Purpose:	Prevention
Official Title:	A Multicentre, Two-part, Randomised, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Tolerability and Pharmacokinetics of the iNOS Inhibitor GW274150 Administered up to 120mg Daily for 12 Weeks in the Prophylactic Treatment of Migraine.
Study Start Date :	October 2005
Actual Primary Completion Date :	September 2007
Actual Study Completion Date :	September 2007

Arms and Interventions

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Arm	Intervention/treatment
Experimental: Arm 1; GW274150 - 5mg or 30mg	Drug: GW274150; The tablets used in this study will contain either 5mg or 30mg of GW274150 Other: Placebo; Placebo to Match GW274150
Placebo Comparator: Arm 2; Placebo to match GW274150	Drug: GW274150; The tablets used in this study will contain either 5mg or 30mg of GW274150 Other: Placebo; Placebo to Match GW274150

Outcome Measures

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Primary Outcome Measures :

1. Occurrence of a migraine headache day on each day during the 4-week baseline period and the 12-week treatment period. [ Time Frame: 12 Weeks ]

Secondary Outcome Measures :

1. Change from baseline in the number of migraine headache days, migraine attacks, mean peak migraine pain severity and mean migraine headache duration for each 4 week treatment period and over the entire treatment period. [ Time Frame: 12 Weeks ]

Eligibility Criteria

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Ages Eligible for Study:	18 Years to 55 Years (Adult)
Sexes Eligible for Study:	Female
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

• Suffering from migraine with or without aura.
• Migraine for at least one year, and the age of onset was prior to 50 years.
• Consistent migraine headache over time and has had at least 3 migraine headache attacks but less than 15 days with headache (migraine or non-migraine) per month in each of the three months prior to the Screening Visit and maintains this requirement during the baseline period.
• Able to distinguish migraine headache attacks as discreet attacks from other headaches (i.e. tension-type headaches).
• No clinically significant abnormality identified on the medical or laboratory evaluation. A subject with a clinical abnormality or laboratory parameters outside the reference range may be included only if the doctor considers that the finding will not introduce additional risk factors and will not interfere with the study procedures.
• Written informed consent prior to entry into the study.
• Females who are: a) non-childbearing potential or, b) of child-bearing potential, has a negative pregnancy test at screen, and is taken adequate contraceptive measures.

Exclusion Criteria:

• As a result of the medical interview, physical examination or screening investigations, that the doctor considers the subject unfit for the study.
• Headache for 15 days per month or greater in any of the three months (90 days) preceding the Screening Visit.
• History of alcohol, substance or drug abuse within the last year.
• Taken a migraine prophylactic medication within 1 month of the Screening Visit.
• Uses an opiate as first line acute treatment for migraine attacks.
• History of ergotamine, triptan, opioid, or combination medication intake on greater than/equal 10 days per month on a regular basis for greater than/equal 3 months.
• History of simple analgesic intake on greater than/equal 15 days per month for greater than/equal 3 months.
• Failed two or more adequate treatments of migraine prophylaxis, where failure is defined as a lack of efficacy with a treatment duration of at least 8 weeks or withdrawal of treatment due to treatment intolerance.
• Uncontrolled hypertension at the Screening Visit, defined as systolic blood pressure >140mmHg or diastolic blood pressure >90mmHg.
• Taking cyclosporine and/or aminoglycosides.
• Evidence of renal impairment - calculated creatinine clearance <60ml/min or clinically relevant finding on urinalysis.
• History of drug or other allergy which, in the opinion of the doctor, makes the subject unsuitable for participation in the study.
• Concurrently participating in another clinical study or investigational drug trial or has participated within the previous 3 months or is planning to participate in another drug or device study at any time during this study (screening through follow-up) or has had previous exposure to GW274150 in Part 1 of the study.
• Felt to be at risk of non-compliance (for taking study medication or for completing the electronic diary (e-diary)), in the doctor's opinion.
• Pregnant or nursing women.
• History of, or risk factors for, HIV, Hepatitis B and Hepatitis C.
• Past or present disease, which as judged by the doctor, may affect the outcome of this study. These diseases include, but are not limited to history of liver or renal disease in the 6 months prior to screening.
• Clinically significant abnormalities in safety laboratory analysis at the Screening Visit, particularly any abnormal liver or pancreatic function test at the Screening Visit.
• Not covered by social security.

Contacts and Locations

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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

  Show 62 Study Locations

Sponsors and Collaborators

GlaxoSmithKline

Investigators

Study Director:	GSK Clinical Trials	GlaxoSmithKline

More Information

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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party:	GlaxoSmithKline
ClinicalTrials.gov Identifier:	NCT00242866 History of Changes
Other Study ID Numbers:	NOS103325
First Posted:	October 21, 2005
Last Update Posted:	May 9, 2016
Last Verified:	September 2015

Keywords provided by GlaxoSmithKline:

Migraine; Productivity; Efficacy; without aura; iNOS; Safety	Nitric Oxide; Pharmacokinetics; GW274150; with aura; Prophylaxis; Quality of Life

Additional relevant MeSH terms:

Migraine Disorders; Headache Disorders, Primary; Headache Disorders	Brain Diseases; Central Nervous System Diseases; Nervous System Diseases