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Exploring Outcomes and Characteristics of Myasthenia Gravis 2
NCT06002945 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this prospective observational study is to create a network repository of clinical data and biological samples to help researchers learn more about myasthenia gravis.
Conditions Studied
Interventions
- OTHER Blood sample
Study Locations (10)
North Carolina
- University of North Carolina — Chapel Hill
- Duke University Medical Center — Durham
- Wake Forest University — Winston-Salem
California
- University of California-Irvine — Irvine
- Cedars Sinai Medical Center — Los Angeles
Connecticut
- Yale University — New Haven
District of Columbia
- George Washington University — Washington D.C.
Illinois
- University of Chicago — Chicago
Massachusetts
- Massachusetts General Hospital — Boston
South Carolina
- Medical University of South Carolina — Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2021-01-12 |
| Est. Completion | 2026-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06002945
The ClinicalTrials.gov registry entry for NCT06002945 describes a study currently listed as active not 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 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,283 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 Myasthenia Gravis appearing as the primary indexed condition, and to 1 intervention — of which Blood sample 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: NCT06002945 reports 10 study locations spanning 7 distinct geographic areas — top geographies include North Carolina, California, Connecticut. 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 NCT06002945 about?
NCT06002945 is a clinical study titled "Exploring Outcomes and Characteristics of Myasthenia Gravis 2". The goal of this prospective observational study is to create a network repository of clinical data and biological samples to help researchers learn more about myasthenia gravis.
What is the current status of trial NCT06002945?
This trial is currently active not recruiting. The enrollment target is 400 participants. The study started on 2021-01-12. Estimated completion is 2026-12.
What conditions does trial NCT06002945 study?
This clinical trial studies the following conditions: Myasthenia Gravis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06002945?
The interventions under investigation include: Blood sample (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06002945?
This trial is sponsored by Yale University, which has 1,283 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06002945 being conducted?
This trial has 10 study locations across California, Connecticut, District of Columbia, Illinois, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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