Dose Comparison Study of Topiramate in Pediatric Subjects With Basilar/Hemiplegic Migraine

Inclusion Criteria:

• Must meet International Headache Society (IHS) classification of pediatric migrainewith aura: familial hemiplegic migraine (International Classification of HeadacheDisorders [ICHD] 1.2.4), sporadic hemiplegic migraine (ICHD 1.2.5) or basilar-typemigraine (ICHD 1.2.6).

• Average of 4 migraine-days/month during the 3 months prior to screening.

• 4 migraine-days during prospective baseline period.

• At least one of the subject's migraines during the previous 3 months must have beenaccompanied by their characteristic basilar-type or hemiplegic neurologic symptoms ofmoderate to severe degree.

• 6-18 years of age.

• Weigh more than 25 kg.

• If female, subjects must:

1. be premenarchal or otherwise incapable of pregnancy, or

2. have practiced one of the following methods of contraception for at least onemonth prior to study entry: hormonal contraceptives, spermicide and barrier,intrauterine device, spousal/partner sterility, or

3. be practicing abstinence and agree to continue abstinence or to use an acceptablemethod of contraception (as listed above) should sexual activity commence. If (b) or (c), the subject must have a negative urine pregnancy test within one week ofstudy entry.

• Able to take oral medication in tablet form

• Willing and able to:

1. read and comprehend written instructions,

2. complete the assessment forms,

3. return for regular visits, and d) adhere to medication regimens.

Exclusion Criteria:

• Previously failed topiramate therapy for migraine prophylaxis or those whodiscontinued topiramate due to adverse events.

• Have taken topiramate within 14 days prior to the start of the prospective baselineperiod.

• Have 15 or more headache-days during the prospective baseline period.

• Have cluster headaches or chronic migraine.

• Have migraine aura without headache exclusively.

• Currently have a more painful condition than their migraine pain.

• Have taken any medications for migraine prophylaxis, within 2 weeks of the start ofthe prospective baseline period.

• Progressive neurological disorders or a structural disorder of the brain

• Overuse analgesic or migraine-specific agents for abortive treatment of migraine:

• >10 treatment days/month of ergot-containing medication, triptans, or opioids;

• >15 treatment days/month with simple analgesics (including NSAIDs)

• Require any injections of corticosteroids or local anesthetics within 60 days of visit 1 or botulinum toxin within 120 days prior to Visit 1.

• Have previously failed more than 2 adequate trials of an established prophylacticanti-migraine regimen.

• Subjects starting non-pharmacologic prophylactic approaches within 1 month prior toVisit 1. Non-pharmacologic prophylactic approaches started at least 1 month prior toVisit 1 should be continued throughout the study.

• Have taken carbonic anhydrase inhibitors or triamterene within 1 month prior to Visit

• History of nephrolithiasis.

• Require continuing treatment with anticonvulsant therapy for a non-migraine condition.

• Significant major psychiatric disorder (e.g., major depression) or subjects receivinganti-psychotic medication.

• History of attempted suicide or suicidal tendencies.

• History of substance abuse.

• Pregnant or lactating females.

• Clinically unstable neurological, cardiovascular, gastrointestinal, musculoskeletal,pulmonary or other disease.

• Active liver disease.

• AST and/or ALT levels greater than 2 times the upper limit of normal range.

• Received an investigational drug or used an investigational device within 30 days ofstudy entry.