CMVIG Prophylaxis in Belatacept Conversion Kidney Transplant Recipients
Recruiting now · Phase 1/Phase 2
Conditions studied: Kidney Transplant; Complications, CMV
In brief
The purpose of this study is to study how CMVIG interacts with the body and to see if it might work to prevent kidney transplant patients from becoming infected with CMV.
Key facts
- Study ID
- NCT07096453
- Run by
- University of Minnesota
- People needed
- 30
- Starts
- 2025-10-02
- Expected to finish
- 2027-08-01
- Last updated by the study team
- 2025-10-31
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult (18-70 year old) kidney transplant recipients
- Patients transitioning from conventional CNI-based immunosuppression to co-stimulatory blockade (belatacept) immunosuppression OR patients who are stable on belatacept immunosuppression at the time of initial CYTOGAM infusion
- CMV Ig Seronegative Recipient who received a CMV Ig seropositive Donor
- EBV IgG Positive
You may not qualify if…
- Pregnant people
- Subjects unwilling to sign consent and complete follow up visits
- Subjects with IgA immunodeficiency
- Subjects who are receiving IgG therapy or who have received IgG therapy within two months of study enrollment
- Patients who do not speak English and would need a translator and translated consent materials in order to obtain informed consent
Where it is running
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
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