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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
The purpose of this study is to determine whether a repeat dose administration of ATIR101 is safe and effective when infused in patients with a hematologic malignancy following a T-cell depleted stem cell graft from a related haploidentical donor. All patients are planned to receive two ATIR101 doses of 2×10E6 viable T-cells/kg, unless the second dose is reduced or halted for safety reasons.
Study CR-AIR-008 is an exploratory, open-label, multicenter study. After signing informed consent, patients will receive a hematopoietic stem cell transplantation (HSCT) from a related, haploidentical donor, followed by a first ATIR101 infusion at a dose of 2×10E6 viable T-cells/kg between 28 and 32 days after the HSCT. Patients will receive a second ATIR101 infusion at a dose of 2×10E6 viable T-cells/kg between 70 and 74 days after the HSCT. To evaluate safety of the second dose administration, the first 6 patients treated will be evaluated for the occurrence of dose limiting toxicity (DLT), defined as acute GvHD grade III/IV within 120 days post HSCT (or within 42 days after the second ATIR101 infusion in case of prior dose delays). If within the first 6 patients no DLT is observed, treatment of the remaining 9 patients will continue with two ATIR101 doses of 2×10E6 viable T cells/kg. If within the first 6 patients at least 2 patients show DLT, the second ATIR101 infusion will be adjusted to a dose of 1×10E6 viable T cells/kg. If in one of the next 3 patients treated at this lower dose again DLT is observed, the second ATIR101 infusion will be halted and the remaining patients will be given only a single dose of ATIR101. All patients treated with ATIR101 will be followed up until 12 months after the HSCT. Assessments will be performed at weekly visits from the day of the first ATIR101 infusion (Week 4) until 6 weeks after the second ATIR101 infusion (Week 16), at monthly visits from 4 until 6 months after the HSCT, and every 3 months from 6 until 12 months after the HSCT.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Algemeen Ziekenhuis Sint-Jan
Bruges, Belgium
Institut Jules Bordet
Brussels, Belgium
Universitair Ziekenhuis Gasthuisberg
Leuven, Belgium
Centre Hospitalier Universitaire de Liège
Liège, Belgium
Juravinski Hospital and Cancer Centre
Hamilton, Ontario, Canada
Maisonneuve-Rosemont Hospital
Montreal, Quebec, Canada
University Hospital Centre Zagreb
Zagreb, Croatia
University Medical Center Mainz
Mainz, Germany
Hospital de Santa Maria, Clinica Universitaria Hematologia
Lisbon, Portugal
Heartlands Hospital
Birmingham, United Kingdom
Start Date
October 9, 2015
Primary Completion Date
July 1, 2018
Completion Date
December 17, 2018
Last Updated
May 18, 2021
15
ACTUAL participants
ATIR101
BIOLOGICAL
Haploidentical hematopoietic stem cell transplantation (HSCT)
PROCEDURE
TBI regime
PROCEDURE
Non-TBI regime
PROCEDURE
Lead Sponsor
Kiadis Pharma
NCT06285890
NCT06220162
NCT05376111
Data Source & Attribution
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