Efgartigimod in Kidney Transplant Recipients With AMR - SHAMROCK

Efgartigimod in Kidney Transplant Recipients With AMR - SHAMROCK

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Purpose of this Study

We are doing this study to find out if an experimental drug called efgartigimod (the study drug) is a safe and effective option for people experiencing kidney rejection. We want to know if it can decrease antibody-mediated rejection following a transplant by removing the antibodies that target and damage the cells of the donated kidney.

Who Can Participate?

Eligibility

Adults ages 18-80 who:
  • Received a kidney transplant at least 6 months ago
  • Are diagnosed with biopsy-confirmed antibody-mediated rejection
  • Are using an immunosuppressing medication for maintenance following their transplant
For more information, contact the study team at lynnette.moats@duke.edu.

Age Range

18-80

Sex/Genders

Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No

What is Involved?

Description

If you choose to join this study, you will get a random assignment (fair, equal chance) to 1 of 3 groups. Depending on your group assignment, you may:
  • Take the study drug for 48 weeks; OR
  • Take a placebo (inactive substance with no drug in it) for 48 weeks; OR
  • Take a combination of the study drug (first 24 weeks) and a placebo (second 24 weeks)
The study will last for about 20 months, and it involves at least 20 study visits. The study visits will include the following procedures: study drug injections, physical exams, blood draws, biopsies, chest x-ray, electrocardiograms, and genetic tests.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

No

Spanish Materials Available

No

Study Details

Full Title

A Multicenter, Randomized, Double-Blinded, Placebo-Controlled,
Phase 2 Study to Evaluate the Safety, Tolerability, and Efficacy of
Efgartigimod in Kidney Transplant Recipients With
Antibody-Mediated Rejection

Principal Investigator

Goni
Katz-Greenberg

Protocol Number

PRO00116061

NCT ID

NCT06503731

Phase

II

Enrollment Status

Pending Open to Enrollment