Safety and Efficacy Study of Human T Lymphoid Progenitor (HTLP) Injection After Partially HLA Compatible Allogeneic Hematopoietic Stem Cell Transplantation in SCID Patients — HTLP Necker

Pediatric Patients Clinical Trial

Official title:
A Phase I/II Study Evaluating the Safety and the Efficacy of Human T Lymphoid Progenitor (HTLP) Injection to Accelerate Immune Reconstitution After Partially HLA Compatible Allogeneic Hematopoietic Stem Cell Transplantation in SCID Patients

Status Recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the safety and the efficacy of Human T Lymphoid Progenitor (HTLP) injection to accelerate immune reconstitution after partially HLA compatible allogeneic hematopoietic stem cell transplantation in SCID patients.

Clinical Trial Description

Not provided ;

Study Design

Related Conditions & MeSH terms

Any Type of Severe Combined Immunodeficiency (SCID)
Partial HLA Incompatible Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)
Pediatric Patients
Severe Combined Immunodeficiency

Clinical Trial Details

NCT number	NCT03879876
Study type	Interventional
Source	Assistance Publique - Hôpitaux de Paris
Contact	Marina CAVAZZANA, MD & PhD
Phone	+33 1 44 49 50 68
Email	m.cavazzana@aphp.fr
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	May 13, 2020
Completion date	June 3, 2025

View Details

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