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RECRUITING

Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in Adult Participants With Migraine

NCT06543914 · View on ClinicalTrials.gov ↗

Study Summary

Migraine is a neurological disease characterized by moderate or severe headache, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will evaluate the effectiveness of atogepant in treating adult participants with migraine in a real-world setting. Atogepant is an approved drug for preventive treatment of migraine in adults. Approximately 1000 adult participants who are prescribed atogepant by their doctors will be enrolled in this study across the world. Participants will receive atogepant oral tablets as prescribed per standard clinical practice and will be followed for 2 years. 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 (20)

New York

  • Dent Neurologic Institute - Amherst /ID# 267606 — Amherst
  • Northwell Health - Great Neck /ID# 280705 — Great Neck
  • Northwell Health /ID# 267596 — New York

Alabama

  • Neurology and Neurodiagnostics of Alabama /ID# 267614 — Hoover
  • Rehabilitation & Neurological Services /ID# 267612 — Huntsville

California

  • Kenneth Martinez MD, A Medical Corp /ID# 267834 — Aliso Viejo
  • Los Angeles Headache Center /ID# 267570 — Los Angeles

Brussels Capital

  • Cliniques Universitaires UCL Saint-Luc /ID# 270545 — Brussels
  • Universitair Ziekenhuis Brussel /ID# 269799 — Jette

Liege

  • Centre Hospitalier Régional de la Citadelle /ID# 270539 — Liège
  • Groupe Sante CHC - Clinique du MontLegia /ID# 270218 — Liège

Arizona

  • Barrow Neurological Institute - Dignity Health St. Joseph's Hosp and Medical Ctr /ID# 267610 — Phoenix

Florida

  • Alcanza Clinical Research, LLC /ID# 267838 — Lake Mary

Kentucky

  • Norton Cancer Institute - St. Matthews /ID# 267605 — Louisville

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2024-11-26
Est. Completion 2029-02

Sponsor

AbbVie

603 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06543914

The ClinicalTrials.gov registry entry for NCT06543914 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 603 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06543914 reports 20 study locations spanning 14 distinct geographic areas — top geographies include New York, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06543914 about?

NCT06543914 is a clinical study titled "Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in Adult Participants With Migraine". Migraine is a neurological disease characterized by moderate or severe headache, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will evaluate the effectiveness of atogepant in treating adult participants with migraine in a real-world setting. Atogepant is an app...

What is the current status of trial NCT06543914?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2024-11-26. Estimated completion is 2029-02.

What conditions does trial NCT06543914 study?

This clinical trial studies the following conditions: Migraine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT06543914?

This trial is sponsored by AbbVie, which has 603 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06543914 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Florida, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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