Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Dose-finding Trial With Lu-AG09222 in Adults With Migraine Who Have Not Been Helped by Prior Preventive Treatments
NCT06323928 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this trial is to determine which doses of Lu AG09222 are recommended to help prevent migraines. People who join this trial have already tried 1 to 4 other available medications to prevent their migraines, but these medications have not helped them.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Lu AG09222
Study Locations (20)
Florida
- K2 Medical Research - Winter Garden — Clermont
- Clinical Neuroscience Solutions, Inc. — Jacksonville
- K2 Medical Research, LLC - Maitland — Maitland
- Aqualane Clinical Research — Naples
- K2 Medical Research Tampa LLC — Tampa
- Premiere Research Institute Palm Beach — West Palm Beach
California
- Profound Research - Neurology Center of Southern California — Carlsbad
- Neurology Center of North Orange County — Fullerton
- CenExel CNS — Los Alamitos
- ASCLEPES Research Centers — Sherman Oaks
North Carolina
- Accellacare of Cary - Cary Medical Group — Cary
- Headache Wellness Center — Greensboro
- Raleigh Medical Group — Raleigh
Missouri
- Clinical Research Professionals — Chesterfield
- Healthcare Research Network — Hazelwood
New York
- Dent Neurosciences Research Center, Inc. — Amherst
- North Suffolk Neurology, PC. — Port Jefferson Station
Alabama
- Accel Research Sites Network - Neurology and Neurodiagnostic of Alabama — Hoover
Connecticut
- Ki Health Partners LLC DBA New England Institute for Clinical Research — Stamford
Iowa
- Accellacare and McFarland Clinic — Ames
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 874 participants |
| Start Date | 2024-04-01 |
| Est. Completion | 2026-04-30 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06323928
The ClinicalTrials.gov registry entry for NCT06323928 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 874 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is H. Lundbeck A/S, which has 17 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 2 interventions — of which Placebo is the first listed. 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: NCT06323928 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, North Carolina. 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 NCT06323928 about?
NCT06323928 is a clinical study titled "A Dose-finding Trial With Lu-AG09222 in Adults With Migraine Who Have Not Been Helped by Prior Preventive Treatments". The purpose of this trial is to determine which doses of Lu AG09222 are recommended to help prevent migraines. People who join this trial have already tried 1 to 4 other available medications to prevent their migraines, but these medications have not helped them.
What is the current status of trial NCT06323928?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 874 participants. The study started on 2024-04-01. Estimated completion is 2026-04-30.
What conditions does trial NCT06323928 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.
What interventions are being tested in trial NCT06323928?
The interventions under investigation include: Placebo (DRUG), Lu AG09222 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06323928?
This trial is sponsored by H. Lundbeck A/S, which has 17 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06323928 being conducted?
This trial has 20 study locations across Alabama, California, Connecticut, Florida, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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