CompletedPhase 2NCT02500550
Safety and Efficacy of Two Doses of ATIR101, a T-lymphocyte Enriched Leukocyte Preparation Depleted of Host Alloreactive T-cells, in Patients With a Hematologic Malignancy Who Received a Hematopoietic Stem Cell Transplantation From a Haploidentical Donor
Studying Acute myeloid leukemia with 11q23 abnormalities
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Kiadis Pharma
- Principal Investigator
- Denis Claude Roy, Prof MDMaisonneuve-Rosemont Hospital (Montreal, Canada)
- Intervention
- ATIR101(biological)
- Enrollment
- 15 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2015 – 2018
Study locations (11)
- 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
- Hammersmith Hospital, London, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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