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Survival and Dialysis Independency in Highly Sensitized Patients After Desensitization With Imlifidase and Tx of Kidneys
NCT05714514 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this follow-up study is to learn about long-term patient survival and graft function in highly sensitized patients who have received desensitization treatment with imlifidase or standard of care (SoC) in order to enable kidney transplantation in clinical study ConfIdeS (20-HMedIdeS-17, NCT04935177).
Conditions Studied
Interventions
- DRUG Imlifidase administered in the ConfIdeS study
- OTHER Best available treatment administered in the ConfIdeS study
Study Locations (14)
Illinois
- Northwestern University, Dept. General Surgery, Div. Transplantation — Chicago
- University of Chicago, Department of Surgery, Clinical Research Center — Chicago
New York
- New York University (NYU) Langone Transplant Institute, NYU Langone Health — New York
- Columbia University — New York
Texas
- Houston Methodist Hospital — Houston
- Methodist Hospital Specialty and Transplant — San Antonio
Alabama
- University of Alabama at Birmingham (UAB) Hospital — Birmingham
California
- Cedars-Sinai Medical Center — Los Angeles
Maryland
- John Hopkins Hospital — Baltimore
Massachusetts
- Massachusetts General Hospital — Boston
Missouri
- Washington University School of Medicine — St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2023-04-21 |
| Est. Completion | 2029-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05714514
The ClinicalTrials.gov registry entry for NCT05714514 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 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hansa Biopharma AB, which has 3 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 Kidney Transplantation in Highly Sensitized Patients appearing as the primary indexed condition, and to 2 interventions — of which Imlifidase administered in the ConfIdeS study 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: NCT05714514 reports 14 study locations spanning 11 distinct geographic areas — top geographies include Illinois, New York, Texas. 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 NCT05714514 about?
NCT05714514 is a clinical study titled "Survival and Dialysis Independency in Highly Sensitized Patients After Desensitization With Imlifidase and Tx of Kidneys". The goal of this follow-up study is to learn about long-term patient survival and graft function in highly sensitized patients who have received desensitization treatment with imlifidase or standard of care (SoC) in order to enable kidney transplantation in clinical study ConfIdeS (20-HMedIdeS-17, N...
What is the current status of trial NCT05714514?
This trial is currently active not recruiting. The enrollment target is 64 participants. The study started on 2023-04-21. Estimated completion is 2029-12-31.
What conditions does trial NCT05714514 study?
This clinical trial studies the following conditions: Kidney Transplantation in Highly Sensitized Patients. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05714514?
The interventions under investigation include: Imlifidase administered in the ConfIdeS study (DRUG), Best available treatment administered in the ConfIdeS study (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05714514?
This trial is sponsored by Hansa Biopharma AB, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05714514 being conducted?
This trial has 14 study locations across Alabama, California, Illinois, Maryland, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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