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Efficacy and Safety Study of Narsoplimab in Pediatric Patients With High-Risk Hematopoietic Stem Cell Transplant TMA
NCT05855083 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the safety and efficacy of narsoplimab in pediatric patients with thrombotic microangiopathies (TMA) following hematopoietic stem cell transplant (HSCT).
Conditions Studied
Interventions
- DRUG Biological: narsoplimab
Study Locations (16)
Other
- Omeros Investigational Site — Halle
- Omeros Investigational Site — Hanover
- Omeros Investigational Site — Haifa
- Omeros Investigational Site — Jerusalem
- Omeros Investigational Site — Ramat Gan
- Omeros Investigational Site — Tel Aviv
- Omeros Investigational Site — Utrecht
- Omeros Investigational Site — Pamplona
New York
- Omeros Investigational Site — New York
- Omeros Investigational Site — Valhalla
California
- Omeros Investigational Site — San Diego
Florida
- Omeros Investigational Site — Gainesville
Massachusetts
- Omeros Investigational Site — Boston
Missouri
- Omeros Investigational Site — St Louis
Texas
- Omeros Investigational Site — Houston
Washington
- Omeros Investigational Site — Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2023-05-01 |
| Est. Completion | 2025-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05855083
The ClinicalTrials.gov registry entry for NCT05855083 describes a study currently listed as 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 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Omeros Corporation, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Hematopoietic Stem Cell Transplantation appearing as the primary indexed condition, and to 1 intervention — of which Biological: narsoplimab 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: NCT05855083 reports 16 study locations spanning 8 distinct geographic areas — top geographies include Other, New York, California. 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 NCT05855083 about?
NCT05855083 is a clinical study titled "Efficacy and Safety Study of Narsoplimab in Pediatric Patients With High-Risk Hematopoietic Stem Cell Transplant TMA". The purpose of this study is to evaluate the safety and efficacy of narsoplimab in pediatric patients with thrombotic microangiopathies (TMA) following hematopoietic stem cell transplant (HSCT).
What is the current status of trial NCT05855083?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2023-05-01. Estimated completion is 2025-12.
What conditions does trial NCT05855083 study?
This clinical trial studies the following conditions: Hematopoietic Stem Cell Transplantation, Thrombotic Microangiopathies. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05855083?
The interventions under investigation include: Biological: narsoplimab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05855083?
This trial is sponsored by Omeros Corporation, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05855083 being conducted?
This trial has 16 study locations across California, Florida, Massachusetts, Missouri, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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