A Double Blind Placebo-controlled, Parallel Group Study to Assess the Efficacy and Safety of Frovatriptan in the Acute Treatment of Migraine

NCT00821483 | Completed Phase 3 DMC

• 1 other identifier: FRESH
• Study Type: interventional
• Target: 298
• Locations: 0 countries
• Sites: N/A

Brief Summary

The purpose of this study is:

1. 1.To compare the efficacy of a single dose of Frovatriptan 2.5 mg with that of placebo in acute treatment of up to one migraine attract
2. 2.To assess recurrence rate between two group
3. 3.To assess the safety and tolerability

Conditions

Migraine

Outcome Measures

Primary Outcomes (1)

• A comparison between Frovatriptan and placebo for the proportion of patients who have complete(grade 0) or almost complete(grade 1) relief of headache at 2 hours after taking Frovatriptan

  at 2 hours

Study Arms (2)

1: placebo

PLACEBO COMPARATOR

Drug: Frovatriptan

2 Frovatriptan

ACTIVE COMPARATOR

Drug: Frovatriptan

Interventions

Frovatriptan DRUG

2.5mg, qd

1: placebo; 2 Frovatriptan

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adults aged 18 to 65 years
• The patients must have a history of migraine according to the criteria of the Headache Classification Committee of the International Headache Society(IHS), over the previous 1 year. The patient must have experienced one to eight moderate or severe migraine attacks(with or without aura) each month over at least the previous two months
• Onset of migraine disease must have occurred before the patients was 50 years of age
• Able and willing to sign informed consent, and able and willing to comply with study procedures, including the completion of diary cards.

You may not qualify if:

• Pregnant or lactating females, or women intend to become pregnant or breast feed during the study period, or women of childbearing potential not using adequate contraception. Females of reproductive potential must have a negative pregnancy test at screening
• Clinically significant renal dysfunction(creatinine≥2.0mg/dl) or hepatic dysfunction(ALT,AST≥2 ULN)
• Patients with clinically significant abnormal ECGs or with resting diastolic blood pressure above 95mmHg
• Patients with clinically significant cardiovascular or cerebrovascular disease
• Patients with a history of clinically relevant allergy, including allergy to triptan
• Previous treatment with Frovatriptan at any time or treatment with an investigational drug within 30 days before screening visit
• Patients with a diagnosis of vertebrobasilar or hemiplegic(prolonged atypical aura) migraine(IHS criteria)
• Potentially unco-operative patients, those unable to provide informed consent, and those unable to complete the diary
• patients who habitually abuse headache medication including ergotamine-containing compounds, and patients with a history of alcohol and/or medicine abuse, in the Investigator's opinion
• Patients who are not able to tell that they are having a migraine headache
• Patients who have 15 or more headache days per month, on average, or those taking symptomatic medication for headaches on more than two days per week, on average
• Treatment with a monoamine-oxidase inhibitor(MAOI) within two weeks of the screening visit
• Patients who are taking prophylactic migraine medication, unless dose has been stabilized for 30 days and it expected to continue for the duration of the study

Sponsors & Collaborators

• SK Chemicals Co., Ltd.: lead

MeSH Terms

Conditions

Migraine Disorders

Interventions

frovatriptan

Condition Hierarchy (Ancestors)

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

Study Officials

• Sun U Kwon, professor

  Department of Neurology, Asan Medical Center, University of Ulsan

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 12, 2009
• First Posted: January 13, 2009
• Study Start: November 1, 2006
• Primary Completion: February 1, 2008
• Study Completion: February 1, 2008
• Last Updated: April 18, 2013

Record last verified: 2013-04