An Exploratory, Open-label, Multicenter Study to Evaluate the Safety and Efficacy of a Two-dose Regimen of ATIR101, a T-lymphocyte Enriched Leukocyte Preparation Depleted ex Vivo of Host Alloreactive T-cells (Using Photodynamic Treatment), in Patients With a Hematologic Malignancy, Who Received a CD34-selected Hematopoietic Stem Cell Transplantation From a Haploidentical Donor
ATIR101, developed by Kiadis Pharma, targets hematologic malignancies post haploidentical stem cell transplantation. The market for hematologic malignancies is substantial, with increasing demand for innovative therapies that reduce transplant-related complications such as graft-versus-host disease (GVHD). The competitive landscape includes other immunotherapies and stem cell transplant approaches. Successful outcomes from this trial could position Kiadis Pharma favorably against competitors, potentially leading to partnerships or acquisition interest. Diligence should focus on regulatory pathways and reimbursement strategies, given the complexity of the treatment regimen and patient population.
Indication: Acute Myeloid Leukemia
Modality: protein therapy
Target: T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreactive T-cells (using photodynamic treatment)
Sponsor: Kiadis Pharma
Source URL: ClinicalTrials.gov
Source updated: May 18, 2021
Ingested: Jun 13, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreactive T-cells (using photodynamic treatment)
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Condition raw: Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Myelodysplastic Syndrome
Condition normalized: Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Myelodysplastic Syndrome
Modality raw: protein therapy
Modality normalized: protein therapy
Target raw: T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreactive T-cells (using photodynamic treatment)
Target normalized: T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreactive T-cells (using photodynamic treatment)