A Randomized Trial of Frovatriptan for the Intermittent Prevention of Menstrual Migraine

Condition(s) targeted: Menstrually Associated Migraine

Intervention: Frovatriptan (Drug); Frovatriptan (Drug); Placebo (Drug)

Phase: Phase 3

Status: Completed

Sponsored by: Endo Pharmaceuticals

Official(s) and/or principal investigator(s):
Arthur Elkind, MD, Principal Investigator

The primary objective of this study was to determine whether frovatriptan was effective in the prevention of menstrually associated migraine (MAM) headaches when compared to placebo. Secondary objectives included determining the effectiveness of frovatriptan in reducing the incidence, severity and duration of MAM headaches and associated symptoms, to evaluate the safety and tolerability of the two frovatriptan dosing regimens and to compare the effectiveness of these regimens in the prevention of MAM headaches. In this cross-over study, patients treated each of 3 perimenstrual periods (PMPs) with placebo, frovatriptan 2. 5 mg daily (QD) and 2. 5 mg twice daily (BID) for 6 days, starting 2 days before the anticipated onset of a MAM headache.

A statistically significant reduction in the incidence of MAM headache (p<0. 0001) was observed with both dosing regimens of frovatriptan when compared to placebo. Additionally, the frovatriptan BID regimen was superior to the frovatriptan QD regimen in the prevention of MAM headache (p<0. 001). Significant reductions in MAM headache severity and duration, the incidence of associated symptoms and characteristics, and the use of rescue medication were observed when the PMP was treated with frovatriptan, compared to placebo. Both dose regimens of frovatriptan were equally well tolerated and no cardiovascular or other safety and tolerability concerns arose with repeated administration of frovatriptan over a 6 day period.

Study design: Prevention, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Safety/Efficacy Study

Primary outcome: Incidence of menstrually associated migraine (MAM) headache in the treated peri-menstrual period (PMP)

Secondary outcome:

Incidence of moderate or severe MAM headaches

Incidence of severe MAM headaches

Duration of MAM headaches

Maximum headache intensity

Incidence of MAM headache associated symptoms and characteristics

Duration of MAM headache associated symptoms

Maximum functional impairment score during MAM headache

Incidence of moderate or severe functional impairment during MAM headache

Duration of moderate or severe functional impairment during MAM headache

Incidence of use of rescue medication for the treatment of a MAM headache

Patient satisfaction score at the end of each 6 day treated PMP

Adverse events

Standard hematology and biochemistry

12-lead ECGs, physical exam, vital signs

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Female.

Criteria:

Inclusion Criteria:

- Females aged 18 years and over

- 12 month or more documented history of menstrual migraine headache, according to

International Headache Society classification

- An average frequency of MAM attacks in at lease 3 out of 4 menstrual cycles

- Regular predictable menstrual periods

- Able to accurately predict the onset of MAM headaches occurring between Day -2 and Day

+4 of menses

- Able and willing to sign informed consent to comply with study procedures, including

completion of diary cards

Exclusion Criteria:

- More than three migraine attacks per month that were not MAM attacks

- Coronary artery disease including coronary vasospasm

- Significant cerebrovascular disease including basilar or hemiplegic migraine

- Uncontrolled hypertension

- Severe hepatic or renal insufficiency

- More than 15 headache days per month

- Any other condition or serious illness which would interfere with optimal

participation in the study

- History of clinically relevant allergy, including that to frovatriptan or other

triptans

- Pregnant or breast feeding or intending to become pregnant or to breast-feed during

study period

- Participated in other frovatriptan menstrual migraine prevention studies

- Use of another investigation drug within 30 days or 5 half-lives (whichever is longer)

before the screening visit

Endo Pharmaceuticals, Chadds Ford, Pennsylvania 19317, United States

Last updated: March 24, 2008