NCT05016661Phase 2Terminated

Extension Study of ABP-20001 to Evaluate Safety and Efficacy of Repeat Treatments of ABP-450 for Migraine Prevention

Study sponsor: AEON Biopharma, Inc. · AEON

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

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Primary completion2024-07-31Actual

Enrollment · participants466Actual

Source updated2024-09-20Last update listed in the registry record

Version history

Changes to this trial

Last 12 months

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No recorded changes are available for this view and time period. Our history may be incomplete; this does not establish that the trial stayed unchanged.

Study details

Conditions studied

Migraine

Treatments or interventions studied

ABP-450DrugAlso known as prabotulinumtoxinA

Primary outcomes · main study measures

Read the study measures

measure: Incidence of Treatment Emergent Adverse Events; description: The primary safety endpoint will be the incidence of TEAEs throughout the study when dosed with ABP-450 (low dose) or ABP-450 (high dose).; timeFrame: Baseline to Week 52 - End of Study; measure: Change in Monthly Migraine Days; description: The primary efficacy endpoint will be the change in mean Monthly Migraine Days (MMD) from Baseline to intervals throughout the study.; timeFrame: Baseline to Week 52 - End of Treatment Period

History coverage

Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.

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