120 Participants NeededMy employer runs this trial

Siplizumab for Kidney Transplant Rejection

(MODERNIZE1 Trial)

Recruiting at 6 trial locations
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Nefro Avillion Clinical Development, LLC
Must be taking: Anti-rejection medicines
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether siplizumab, an experimental therapy, can prevent kidney transplant rejection in individuals with end-stage kidney disease. Participants will divide into three groups: two will receive different doses of siplizumab, and the third will receive rabbit anti-thymocyte globulin (rATG), an existing immunosuppressive drug. The trial aims to assess how well participants' bodies accept the transplanted kidney and compare the effects and safety of siplizumab to rATG. Individuals who recently received a kidney from a living or recently deceased donor and have no history of certain infections or major health issues may qualify for participation. As a Phase 2 trial, this research measures the treatment's effectiveness in an initial, smaller group, allowing participants to contribute to significant advancements in kidney transplant care.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop your current medications, but you will continue taking the usual anti-rejection medicines given before, during, and after a kidney transplant.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that siplizumab is generally safe for people. Studies have found that most individuals tolerate it well, with few serious side effects. In earlier research with kidney transplant patients, siplizumab was considered safe. Safety studies also revealed that siplizumab remains active in the body for a short time after administration, helping to control its effects.

This trial compares two doses of siplizumab to rabbit anti-thymocyte globulin (rATG), with a focus on siplizumab's safety. While specific side effect data from this trial phase is not yet available, past evidence suggests that patients usually tolerate the treatment well.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about siplizumab for kidney transplant rejection because it offers a novel approach to preventing rejection. Unlike the standard treatments, such as rabbit anti-thymocyte globulin, which broadly suppress the immune system, siplizumab specifically targets the CD2 receptor on T cells. This targeted action could mean fewer side effects and a more precise way to prevent the immune system from attacking the transplanted kidney. Additionally, by exploring both low and high doses of siplizumab, researchers hope to optimize its effectiveness and safety.

What evidence suggests that this trial's treatments could be effective for kidney transplant rejection?

This trial will compare siplizumab with rabbit anti-thymocyte globulin to prevent kidney transplant rejection. Research has shown that siplizumab might be a promising option for this purpose. Studies have found that siplizumab is generally safe and may work well with other medications to prevent rejection. Its unique mechanism could make it more effective than some current treatments. Early results suggest it can reduce the activity of certain immune cells that might otherwise attack the new kidney. While more information is needed, these initial findings are encouraging for those considering siplizumab as a treatment option.12356

Are You a Good Fit for This Trial?

This trial is for adults with end-stage kidney disease who are getting a kidney transplant from a living or deceased donor (not an identical twin). The donated kidney must have been kept cold for less than 30 hours. Women able to become pregnant must use effective birth control.

Inclusion Criteria

Women of childbearing potential must agree to use highly effective methods of contraception
I received a kidney transplant from a donor who was not an HLA match.
I received a kidney that was preserved for less than 30 hours before transplant.

Exclusion Criteria

Crossmatch positive (except isolated positive B cell crossmatches)
Presence of current or historical DSA via single-antigen bead assay or local standard of care within 3 months prior to transplant
ABO-incompatible recipient
See 11 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either siplizumab or rATG as induction therapy along with standard immunosuppressive therapy

12 weeks
Multiple visits for treatment administration and monitoring

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessments of adverse events and pharmacokinetics

12 months
Regular visits for safety assessments and laboratory evaluations

Final Analysis

Final analysis performed to evaluate the safety and efficacy of siplizumab compared to rATG

End of study

What Are the Treatments Tested in This Trial?

Interventions

  • Rabbit anti-thymocyte globulin
  • Siplizumab

Trial Overview

The study compares two doses of siplizumab and rabbit anti-thymocyte globulin (rATG) to see which better prevents rejection after a kidney transplant. Participants are randomly assigned to one of three groups, all receiving standard anti-rejection medicines as well.

How Is the Trial Designed?

3

Treatment groups

Experimental Treatment

Active Control

Group I: Low dose siplizumabExperimental Treatment1 Intervention
Group II: High dose siplizumabExperimental Treatment1 Intervention
Group III: Rabbit anti-thymocyte globulinActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Nefro Avillion Clinical Development, LLC

Lead Sponsor

Citations

NCT07508787 | A Study Comparing Siplizumab With ...

The goal of this clinical trial is to learn if siplizumab can prevent rejection of a kidney transplant in adult participants with end stage kidney disease.

Siplizumab - an overview | ScienceDirect Topics

A study examining the safety profile, pharmacokinetics, and pharmacodynamics of siplizumab in renal allograft recipients showed an acceptable safety profile.

Siplizumab combination therapy with belatacept or ...

Given its unique binding and mechanisms of action, siplizumab may offer a more effective rejection prevention option than alefacept when combined with CTLA4-Ig.

Study of Siplizumab-Based Treatment in Patients ... - RecruitMe

The purpose of this research study is to see if the anti-rejection medications that patients normally take after transplant can be reduced or stopped completely ...

TCD601 for Kidney Transplant Rejection Prevention

After the first dose, the treatment reduced NK cell activity, but this effect diminished by day 33. 83.4% and 91.5%, respectively,

6.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/19917362/

Safety profile, pharmacokinetics, and pharmacodynamics ...

Siplizumab exhibited an acceptable safety profile in this study. Detectable siplizumab concentrations were maintained for 3 days after the second dose