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Clinical Trials/NL-OMON48626
NL-OMON48626
Completed
Phase 3

Randomized Controlled Trial of Lasmiditan Over Four Migraine Attacks - H8H-MC-LAIJ

Eli Lilly0 sites37 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Headache
Sponsor
Eli Lilly
Enrollment
37
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Eli Lilly

Eligibility Criteria

Inclusion Criteria

  • \- Are of an acceptable age to provide informed consent according to the local regulations and are at least 18 years of age at time of screening (Visit 1\) with migraine with or without aura fulfilling the IHS (International Headache Society) diagnostic criteria 1\.1 or 1\.2\.1\.
  • \- History of disabling migraine for at least 1 year.
  • \- Migraine onset before the age of 50 years.
  • \- History of 3 to 8 migraine attacks per month (\< 15 headache days per month).
  • \- MIDAS score \>\=11\.
  • \- Able and willing to complete an eDiary to record the details of each migraine attack treated with study drug.
  • \- women of child\-bearing potential must agree to use a highly effective method of contraception (that is, one with less than 1% failure rate) such as combination oral contraceptives, implanted/ injected contraceptives, intrauterine devices, or sterile partner until 30 days after the last dose of study medication.
  • \- Agree not to post any personal medical data or information related to the study on any website or social media site until the entire trial has completed.
  • \- Are able and willing to give signed informed consent

Exclusion Criteria

  • \-Known hypersensitivity to lasmiditan, or to any excipient of lasmiditan oral tablets
  • \- increased risk of seizures
  • \-History of recurrent dizziness and/or vertigo
  • \-History of diabetes mellitus with complications
  • \-History of orthostatic hypotension with syncope
  • \-Significant renal or hepatic impairment
  • \-Patients who, in the investigator\*s judgment, are actively suicidal
  • \-History, within past 12 months, of chronic migraine or other forms of primary or secondary chronic headache disorder (eg, hemicranias continua, medication overuse headache where headache frequency is \>\=15 headache days per month
  • \- Use of more than 3 doses per month of either opioids or barbiturates
  • \- Initiation of or a change in concomitant medication to reduce the frequency of migraine episodes within 3 months prior to Screening/Visit 1

Outcomes

Primary Outcomes

Not specified

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