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NCT06958796 · ClinicalTrials.gov registry record · Phase 4

Strategic Help With Immunoglobulin to Enhance Protect Against Late Disease (CMV)

A Phase 4 study of Kidney Transplant; Complications and Liver Transplant, Complications, sponsored by Camille N. Kotton, MD.

Recruiting
Registry status
Phase 4
Development phase
80
Enrollment target
2
Study locations

NCT06958796 is a Phase 4 study of Kidney Transplant; Complications and Liver Transplant, Complications that is actively recruiting participants, run by Camille N. Kotton, MD. The registered enrollment target is 80 participants, below the 118-participant average among 19 other Kidney Transplant; Complications trials with a reported enrollment target (32% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT06958796, a Phase 4 study of Kidney Transplant; Complications and Liver Transplant, Complications, is actively recruiting participants, sponsored by Camille N. Kotton, MD.

RECRUITING
Registry status
Phase 4
Development phase
80 participants
Enrollment target
2
Study locations

Study Summary

This study is being done to find out if administering CytoGam® after the end of standardly prescribed preventive antiviral treatment can help transplant recipients with a high risk for developing late CMV disease after a liver and/or kidney transplant.

Interventions

  • DRUG Cytomegalovirus Immune Globulin Intravenous (Human) monthly for three months

Study Locations (2)

Massachusetts

  • Massachusetts General Hospital - Boston

Texas

  • University of Texas Southwestern - Dallas

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2025-11-27
Est. Completion 2028-05-31
Phase Phase 4

Sponsor

Camille N. Kotton, MD

1 total trials

What the Registry Record Tells You About NCT06958796

The ClinicalTrials.gov registry entry for NCT06958796 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 118-participant average among 19 other Kidney Transplant; Complications trials with a reported enrollment target (32% lower). The listed sponsor is Camille N. Kotton, MD, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Kidney Transplant; Complications appearing as the primary indexed condition, and to 1 intervention - of which Cytomegalovirus Immune Globulin Intravenous (Human) monthly for three months is the first listed.

NCT06958796 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Massachusetts, Texas.

Frequently Asked Questions

What is clinical trial NCT06958796 about?

NCT06958796 is a clinical study titled "Strategic Help With Immunoglobulin to Enhance Protect Against Late Disease (CMV)". This study is being done to find out if administering CytoGam® after the end of standardly prescribed preventive antiviral treatment can help transplant recipients with a high risk for developing late CMV disease after a liver and/or kidney transplant.

What is the current status of trial NCT06958796?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2025-11-27. Estimated completion is 2028-05-31.

What conditions does trial NCT06958796 study?

This clinical trial studies the following conditions: Kidney Transplant; Complications, Liver Transplant, Complications, Cytomegalovirus, Organ Transplant, Simultaneous Liver-Kidney Transplantation; Complications.

What interventions are being tested in trial NCT06958796?

The interventions under investigation include: Cytomegalovirus Immune Globulin Intravenous (Human) monthly for three months (DRUG).

Who is sponsoring clinical trial NCT06958796?

This trial is sponsored by Camille N. Kotton, MD, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06958796 being conducted?

This trial has 2 study locations across Massachusetts, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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