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NCT07310290 · ClinicalTrials.gov registry record

Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks

A clinical trial of Migraine, sponsored by AbbVie.

Recruiting
Registry status
189
Enrollment target
3
Study locations

NCT07310290 is a study of Migraine that is actively recruiting participants, run by AbbVie. The registered enrollment target is 189 participants, below the 356-participant average among 102 other Migraine trials with a reported enrollment target (47% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT07310290, a study of Migraine, is actively recruiting participants, sponsored by AbbVie.

RECRUITING
Registry status
189 participants
Enrollment target
3
Study locations

Study Summary

Migraine is a neurological disease characterized by moderate or severe headaches, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will assess changes in migraine attack severity for adult participants treating with oral ubrogepant across migraine attacks. Ubrogepant is a drug that is approved for the acute treatment of migraine in adults. Approximately 189 participants will be enrolled in approximately 15 sites across the US. Participants will receive ubrogepant as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for up to 13 weeks. There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

Conditions Studied

Study Locations (3)

California

  • Neurology and Pain Specialty Center /ID# 278508 - Aliso Viejo

Illinois

  • Chicago Headache Center & Research Inst /ID# 272345 - Naperville

Nebraska

  • Tri City Research Center, LLC /ID# 278800 - Grand Island

Trial Details

FieldValue
Enrollment Target 189 participants
Start Date 2026-01-27
Est. Completion 2027-03

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT07310290

The ClinicalTrials.gov registry entry for NCT07310290 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 189 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 356-participant average among 102 other Migraine trials with a reported enrollment target (47% lower). The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 0 interventions.

NCT07310290 reports 3 study locations spanning 3 distinct geographic areas - top geographies include California, Illinois, Nebraska.

Frequently Asked Questions

What is clinical trial NCT07310290 about?

NCT07310290 is a clinical study titled "Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks". Migraine is a neurological disease characterized by moderate or severe headaches, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will assess changes in migraine attack severity for adult participants treating with oral ubrogepant across migraine attacks. Ubrogep...

What is the current status of trial NCT07310290?

This trial is currently recruiting. The enrollment target is 189 participants. The study started on 2026-01-27. Estimated completion is 2027-03.

What conditions does trial NCT07310290 study?

This clinical trial studies the following conditions: Migraine.

Who is sponsoring clinical trial NCT07310290?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07310290 being conducted?

This trial has 3 study locations across California, Illinois, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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