Safety and Efficacy of SMART101 in Pediatric and Adult Patients With Hematological Malignancies After T Cell Depleted Allo-HSCT

Recruiting Phase 1 Phase 2 Interventional Study
Hematological Malignancies
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
36 (estimated)
Sponsor
Smart Immune SAS · Industry
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About This Trial

The purpose of this study is to evaluate the safety and the efficacy of SMART101 (Human T Lymphoid Progenitor (HTLP)) injection to accelerate immune reconstitution after T cell depleted allogeneic hematopoietic stem cell transplantation (HSCT) in adult and pediatric patients with hematological malignancies.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: Group A (adults): 1. Adult patients affected by: * Acute leukemia (AML, ALL) defined as: * Acute Myeloid Leukemia (AML): * High risk AML in CR1; any adverse genetic abnormality, secondary or therapy related AML excluding good risk genetic abnormalities …
Contacts

Frédéric LEHMANN, MD

+32 (0) 492 46 23 55

frederic.lehmann@smart-immune.com

CONTACT

Laura SIMONS, MD, PhD

laura.simons@smart-immune.com

CONTACT