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RECRUITING

An Observational Extension Study for Adult Patients Treated in Study R5459-RT-1944 Who Receive a Kidney Transplant

NCT05106387 · View on ClinicalTrials.gov ↗

Study Summary

The main purpose of this study is to continue to see how vonsetamig works in the body and to monitor the outcomes after kidney transplant for participants previously treated in the R5459-RT-1944 study (NCT05092347). No study drug will be given during this study.

Interventions

  • DRUG Noninterventional

Study Locations (9)

California

  • Cedars-Sinai Medical Center — Los Angeles
  • University of California Irvine — Orange
  • Connie Frank Transplant Center at UCSF — San Francisco

Connecticut

  • Yale University of Medicine — New Haven

Illinois

  • Comprehensive Transplant Center — Chicago

Maryland

  • John Hopkins Hospital — Baltimore

Minnesota

  • University of Minnesota — Minneapolis

New York

  • New York University Langone Health — New York

Pennsylvania

  • Penn Transplant Institute — Philadelphia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-10-19
Est. Completion 2027-12-24

Sponsor

Regeneron Pharmaceuticals

290 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05106387

The ClinicalTrials.gov registry entry for NCT05106387 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 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Regeneron Pharmaceuticals, which has 290 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 Chronic Kidney Disease (CKD) appearing as the primary indexed condition, and to 1 intervention — of which Noninterventional 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: NCT05106387 reports 9 study locations spanning 7 distinct geographic areas — top geographies include California, Connecticut, Illinois. 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 NCT05106387 about?

NCT05106387 is a clinical study titled "An Observational Extension Study for Adult Patients Treated in Study R5459-RT-1944 Who Receive a Kidney Transplant". The main purpose of this study is to continue to see how vonsetamig works in the body and to monitor the outcomes after kidney transplant for participants previously treated in the R5459-RT-1944 study (NCT05092347). No study drug will be given during this study.

What is the current status of trial NCT05106387?

This trial is currently recruiting. The enrollment target is 20 participants. The study started on 2023-10-19. Estimated completion is 2027-12-24.

What conditions does trial NCT05106387 study?

This clinical trial studies the following conditions: Chronic Kidney Disease (CKD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05106387?

The interventions under investigation include: Noninterventional (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05106387?

This trial is sponsored by Regeneron Pharmaceuticals, which has 290 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05106387 being conducted?

This trial has 9 study locations across California, Connecticut, Illinois, Maryland, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial