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NCT02605174 · ClinicalTrials.gov registry record · Phase 3

Three Doses of Lasmiditan (50 mg, 100 mg and 200 mg) Compared to Placebo in the Acute Treatment of Migraine

A Phase 3 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 3
Development phase
3,005
Enrollment target

NCT02605174: Completed Phase 3 study, sponsored by Eli Lilly and Company.

NCT02605174 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 3,005 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (289% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02605174, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 3
Development phase
3,005 participants
Enrollment target

Study Summary

This is a prospective randomized, double-blind, placebo-controlled study in participants with disabling migraine (Migraine Disability Assessment (MIDAS) score ≥ 11).

Primary Outcome

The percentage of participants defined as mild, moderate, or severe headache pain becoming none.

Interventions

  • DRUG Placebo
  • DRUG Lasmiditan 50 mg
  • DRUG Lasmiditan 100 mg
  • DRUG Lasmiditan 200 mg

Trial Details

FieldValue
Enrollment Target 3,005 participants
Start Date 2016-05
Est. Completion 2017-06-30
Phase Phase 3
Eli Lilly and Company

1,341 total trials

What the finished NCT02605174 record still lists

NCT02605174 is an interventional study that assigns participants to a tested intervention. Its 3,005 participants enrollment target places it among the larger protocols in the corpus, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (289% higher).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02605174 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02605174 about?

NCT02605174 is a clinical study titled "Three Doses of Lasmiditan (50 mg, 100 mg and 200 mg) Compared to Placebo in the Acute Treatment of Migraine". This is a prospective randomized, double-blind, placebo-controlled study in participants with disabling migraine (Migraine Disability Assessment (MIDAS) score ≥ 11).

What is the current status of trial NCT02605174?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 3,005 participants. The study started on 2016-05. Estimated completion is 2017-06-30.

What interventions are being tested in trial NCT02605174?

The interventions under investigation include: Placebo (DRUG), Lasmiditan 50 mg (DRUG), Lasmiditan 100 mg (DRUG), Lasmiditan 200 mg (DRUG).

Who is sponsoring clinical trial NCT02605174?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02605174's enrollment target sits among peer trials

3,005 79th of 2000 higher than 1,922 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02605174, the US trial registry maintained by the National Library of Medicine. NCT02605174 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.