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Prescreening Study to Identify Potential Stargardt Participants for ACDN-01 Clinical Trials (STARPATH)
NCT06445322 · View on ClinicalTrials.gov ↗
Study Summary
This is an observational prescreening study. Individuals who are eligible for prescreening will undergo testing procedures that may be used to determine eligibility in ACDN-01 clinical trials.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Prescreening Assessments
Study Locations (8)
Texas
- Retina Foundation of Texas — Dallas
- Retina Consultants of Texas — Houston
California
- University of San Francisco — San Francisco
Florida
- Vitreo Retinal Associates — Gainesville
Maryland
- Wilmer Eye Institute at John Hopkins — Baltimore
Massachusetts
- Massachusetts Eye and Ear — Boston
Michigan
- University of Michigan Kellogg Eye Center — Ann Arbor
Ohio
- Cincinnati Eye Institute — Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-06-20 |
| Est. Completion | 2030-08-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06445322
The ClinicalTrials.gov registry entry for NCT06445322 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 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ascidian Therapeutics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Stargardt Disease appearing as the primary indexed condition, and to 1 intervention — of which Prescreening Assessments 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: NCT06445322 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Texas, California, Florida. 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 NCT06445322 about?
NCT06445322 is a clinical study titled "Prescreening Study to Identify Potential Stargardt Participants for ACDN-01 Clinical Trials (STARPATH)". This is an observational prescreening study. Individuals who are eligible for prescreening will undergo testing procedures that may be used to determine eligibility in ACDN-01 clinical trials.
What is the current status of trial NCT06445322?
This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2024-06-20. Estimated completion is 2030-08-31.
What conditions does trial NCT06445322 study?
This clinical trial studies the following conditions: Stargardt Disease, Cone Rod Dystrophy, Stargardt Disease 1, Juvenile Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06445322?
The interventions under investigation include: Prescreening Assessments (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06445322?
This trial is sponsored by Ascidian Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06445322 being conducted?
This trial has 8 study locations across California, Florida, Maryland, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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