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RECRUITING
NCT05768035
PHASE1/PHASE2

Safety and Efficacy of SMART101 in Adult Patients With Hematological Malignancies After Haploidentical HSCT With Post-transplant Cyclophosphamide

Sponsor: Smart Immune SAS

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the safety and the efficacy of SMART101 (Human T Lymphoid Progenitors (HTLP)) injection to accelerate immune reconstitution after haploidentical hematopoietic stem cell transplantation (HSCT) with post-transplant cyclophosphamide (PT-Cy) in adult patients with hematological malignancies.

Official title: An Open-label, Multi-center Phase I/II Study to Assess the Safety and the Efficacy of SMART101 After Haploidentical Peripheral Blood Stem Transplantation With Post-transplant Cyclophosphamide in Subjects With Hematological Malignancies

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2023-06-06

Completion Date

2026-07

Last Updated

2023-09-25

Healthy Volunteers

No

Interventions

BIOLOGICAL

Allogeneic T cell progenitors, cultured ex-vivo

Injection of T cell progenitors 6 days after haplo HSCT and 2 days after the last administration of cyclophosphamide

Locations (4)

Institut Paoli Calmettes

Marseille, France

Centre hospitalier universitaire de Nantes

Nantes, France

Hôpital Saint-Louis

Paris, France

CHU Toulouse- Institut Universitaire du cancer Toulouse- Oncopole

Toulouse, France