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Renal Allograft Tolerance Through Mixed Chimerism

NCT01780454 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2021-04-19

Study results available
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Summary

This study will examine the safety and effectiveness of a combination kidney and bone marrow transplant from a haplo-identical related donor. An investigational medication and other treatments will be given prior to and after the transplant to help protect the transplanted kidney from being attacked by the body's immune system

Conditions

Interventions

DRUG

MEDI-507

T-Cell Depleting Agent

DRUG

Rituximab

B-Cell Depleting Agent

RADIATION

Total Body Irradiation

Bone Marrow Depletion

RADIATION

Thymic Irradiation

Sponsors & Collaborators

  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • A. Benedict Cosimi, M.D. · Massachusetts General Hospital

  • David Sachs, M.D. · Massachusetts General Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2018-06-30
Completion
2020-06-30

Countries

  • United States

Study Locations

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Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01780454 on ClinicalTrials.gov