Survival and Dialysis Independency in Highly Sensitized Patients After Desensitization With Imlifidase and Tx of Kidneys

Description

The goal of this follow-up study is to learn about long-term patient survival and graft function in highly sensitized patients who have received desensitization treatment with imlifidase or standard of care (SoC) in order to enable kidney transplantation in clinical study ConfIdeS (20-HMedIdeS-17, NCT04935177).

Conditions

Kidney Transplantation in Highly Sensitized Patients

Study Overview

Study Details

Study overview

The goal of this follow-up study is to learn about long-term patient survival and graft function in highly sensitized patients who have received desensitization treatment with imlifidase or standard of care (SoC) in order to enable kidney transplantation in clinical study ConfIdeS (20-HMedIdeS-17, NCT04935177).

A Prospective, Long-term Confirmatory Follow up Trial in Highly Sensitized Patients Treated With Imlifidase or Standard of Care in the ConfIdeS (20-HMedIdeS-17) Trial

Survival and Dialysis Independency in Highly Sensitized Patients After Desensitization With Imlifidase and Tx of Kidneys

Condition
Kidney Transplantation in Highly Sensitized Patients
Intervention / Treatment

-

Contacts and Locations

Birmingham

University of Alabama at Birmingham (UAB) Hospital, Birmingham, Alabama, United States, 35249

Baltimore

John Hopkins Hospital, Baltimore, Maryland, United States, 21287

New York

New York University (NYU) Langone Transplant Institute, NYU Langone Health, New York, New York, United States, 10016

New York

Columbia University, New York, New York, United States, 10032

Houston

Houston Methodist Hospital, Houston, Texas, United States, 77030

San Antonio

Methodist Hospital Specialty and Transplant, San Antonio, Texas, United States, 78229

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Signed Informed Consent obtained before any trial-related procedures.
  • 2. Previous participation in the clinical trial ConfIdeS.
  • 1. Inability by the judgement of the investigator to participate in the trial for any reason.

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Hansa Biopharma AB,

Therese Åkerfeldt, STUDY_DIRECTOR, Hansa Biopharma AB

Study Record Dates

2029-12-31