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NCT02956005 · ClinicalTrials.gov registry record · NA

Envarsus XR in African American Renal Transplant Recipients

A NA study, sponsored by Georgetown University.

Terminated
Registry status
NA
Development phase
18
Enrollment target

NCT02956005: Clinical Trial NA study, sponsored by Georgetown University.

NCT02956005 is a NA study that was terminated before completion, run by Georgetown University. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02956005, a NA study, was terminated before completion, sponsored by Georgetown University.

TERMINATED
Registry status
NA
Development phase
18 participants
Enrollment target

Study Summary

The purpose of this study is to collect data prospectively on African American patients who are taking the immunosuppressant Envarsus post kidney transplant. We are looking to see if African American renal transplant recipients that receive Envarsus will have less tubular injury and calcenurin inhibitor toxicity compared with patients that receive tacrolimus IR. African americans have the higher rates of CYP3A5 which is associated with the need of higher tacrolimus dose to achieve an adequate level and this many times is associated with signs and symptoms of tacrolimus toxicity such as tremors, headaches and neuropathies. The retrospective cohort will be African American patients that will be matched by age, gender, type of kidney transplant (living vs deceased) and level of sensitization

Primary Outcome

Data not collected - study terminated prematurely when PI left institution.

Interventions

  • DRUG ENVARSUS®

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2016-09
Est. Completion 2018-09
Phase NA
Georgetown University

227 total trials

Why NCT02956005 stopped before completion

NCT02956005 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which ENVARSUS® is the first listed.

NCT02956005 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02956005 about?

NCT02956005 is a clinical study titled "Envarsus XR in African American Renal Transplant Recipients". The purpose of this study is to collect data prospectively on African American patients who are taking the immunosuppressant Envarsus post kidney transplant. We are looking to see if African American renal transplant recipients that receive Envarsus will have less tubular injury and calcenurin inhib...

What is the current status of trial NCT02956005?

This trial is currently terminated. It is a NA study. The enrollment target is 18 participants. The study started on 2016-09. Estimated completion is 2018-09.

What interventions are being tested in trial NCT02956005?

The interventions under investigation include: ENVARSUS® (DRUG).

Who is sponsoring clinical trial NCT02956005?

This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02956005's enrollment target sits among peer trials

18 1863rd of 2000 higher than 130 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02956005, the US trial registry maintained by the National Library of Medicine. NCT02956005 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.