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A Phase 3 Study of Ersodetug in Patients With Tumor Hyperinsulinism
NCT06881992 · View on ClinicalTrials.gov ↗
Study Summary
The objectives of this study are to evaluate the glycemic efficacy, safety, and tolerability of ersodetug as add-on to standard of care (SOC) therapy for treatment of hypoglycemia in patients with Tumor Hyperinsulinism (Tumor HI).
Conditions Studied
Interventions
- DRUG Ersodetug
Study Locations (13)
Illinois
- Investigative Site — Chicago
Maryland
- Investigative Site — Bethesda
Massachusetts
- Investigative Site — Boston
Minnesota
- Investigative Site — Rochester
New York
- Investigative Site — New York
Ohio
- Investigative Site — Canton
Oregon
- Investigative Site — Portland
Texas
- Investigative Site — Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 16 participants |
| Start Date | 2025-04-16 |
| Est. Completion | 2027-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06881992
The ClinicalTrials.gov registry entry for NCT06881992 describes a study currently listed as recruiting. It is categorized as Phase 3, 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 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rezolute, 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 1 condition, with Tumor Hyperinsulinism (Tumor HI) appearing as the primary indexed condition, and to 1 intervention — of which Ersodetug 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: NCT06881992 reports 13 study locations spanning 13 distinct geographic areas — top geographies include Illinois, Maryland, Massachusetts. 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 NCT06881992 about?
NCT06881992 is a clinical study titled "A Phase 3 Study of Ersodetug in Patients With Tumor Hyperinsulinism". The objectives of this study are to evaluate the glycemic efficacy, safety, and tolerability of ersodetug as add-on to standard of care (SOC) therapy for treatment of hypoglycemia in patients with Tumor Hyperinsulinism (Tumor HI).
What is the current status of trial NCT06881992?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 16 participants. The study started on 2025-04-16. Estimated completion is 2027-09.
What conditions does trial NCT06881992 study?
This clinical trial studies the following conditions: Tumor Hyperinsulinism (Tumor HI). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06881992?
The interventions under investigation include: Ersodetug (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06881992?
This trial is sponsored by Rezolute, 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 NCT06881992 being conducted?
This trial has 13 study locations across Illinois, Maryland, Massachusetts, Minnesota, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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