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RHD Genotype Matched Red Cells for Anti-D

Children's Hospital of Philadelphia (CHOP) logo

Children's Hospital of Philadelphia (CHOP)

Status and phase

Completed
Early Phase 1

Conditions

Anti-D Antibodies
Sickle Cell Disease

Treatments

Biological: D+ RH genotype matched red cell units for transfusion

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04156906
19-016566
R01HL147879-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This is a pilot study to evaluate the feasibility and safety of providing RH genotype matched D+ Red Blood Cells (RBCs) to chronically transfused patients with sickle cell disease (SCD) who type D+ but have formed anti-D and are currently transfused with D- RBC (Red Blood Cell) units.

Full description

Red blood cell transfusion remains a critical therapy for patients with sickle cell disease (SCD). A major problem is the high rate of alloimmunization (antibody formation against transfused red cells) that occurs in patients with SCD. Recent studies performed by Investigators and others demonstrate RH genetic variants in patients and donors is a major risk factor leading to Rh alloimmunization. Anti-D formation in D+ patients occurs frequently, and once identified, providing D- cells for all subsequent transfusions can be challenging. These anti-D antibodies in D+ patients suggest exposure to different or variant D protein on donor cells. Investigators will test whether transfusion of patients with anti-D with RHD genotyped matched red cells is feasible, safe and can decrease D- donor unit demand.

Enrollment

5 patients

Sex

All

Ages

8+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects age > 8 years old
  • Diagnosis of SCD, all genotypes
  • Require chronic red cell transfusion therapy
  • History of anti-D
  • RH genotype predicts D+ expression

Exclusion criteria

  • Rare RH genotype that would preclude sufficient RBC units
  • Antigen negative requirements due to alloimmunization that would preclude sufficient RBC units

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

D+ RH genotype matched Red Blood Cell Transfusion
Experimental group
Description:
Investigators will provide one red cell unit of D+ RH genotype matched RBCs at the first transfusion study visit. The remainder of units will be provided per clinical standard of care, i.e. D-, CEK-matched, and negative for all other antigens the patient is alloimmunized against. If laboratory monitoring shows no reappearance of anti-D and no signs of increased red cell hemolysis, the patient will receive one unit of D+ RH genotype matched RBCs at the 2nd transfusion study visit, and if tolerated, D+ red cell exposures will increase by one unit per study visit until all units required are D+.
Treatment:
Biological: D+ RH genotype matched red cell units for transfusion

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Stella Chou, MD

Data sourced from clinicaltrials.gov

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