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A Study to Evaluate AI-09 In Participants With Glabellar Lines
NCT07321834 · View on ClinicalTrials.gov ↗
Study Summary
Phase 2 clinical study to evaluate the efficacy, safety, and tolerability of AI-09, a Ready-to-Use Liquid Injectable Botulinum Toxin.
Conditions Studied
Interventions
- BIOLOGICAL AI-09 Ready Use Injectable Botulinum Toxin
- BIOLOGICAL Vehicle
Study Locations (5)
Florida
- Center for Clinical and Cosmetic Research — Aventura
- Research Institute of the Southeast, Inc. — West Palm Beach
Louisiana
- Delricht Research — New Orleans
Tennessee
- Tennessee Clinical Research Center — Nashville
Texas
- Research Your Health — Plano
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 68 participants |
| Start Date | 2025-12-03 |
| Est. Completion | 2026-02 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07321834
The ClinicalTrials.gov registry entry for NCT07321834 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 68 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eirion Therapeutics, which has 1 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 Glabellar Lines appearing as the primary indexed condition, and to 2 interventions — of which AI-09 Ready Use Injectable Botulinum Toxin 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: NCT07321834 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Florida, Louisiana, Tennessee. 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 NCT07321834 about?
NCT07321834 is a clinical study titled "A Study to Evaluate AI-09 In Participants With Glabellar Lines". Phase 2 clinical study to evaluate the efficacy, safety, and tolerability of AI-09, a Ready-to-Use Liquid Injectable Botulinum Toxin.
What is the current status of trial NCT07321834?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 68 participants. The study started on 2025-12-03. Estimated completion is 2026-02.
What conditions does trial NCT07321834 study?
This clinical trial studies the following conditions: Glabellar Lines. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07321834?
The interventions under investigation include: AI-09 Ready Use Injectable Botulinum Toxin (BIOLOGICAL), Vehicle (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07321834?
This trial is sponsored by Eirion Therapeutics, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07321834 being conducted?
This trial has 5 study locations across Florida, Louisiana, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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