Safety and Efficacy of ATIR101 as Adjunctive Treatment to Blood Stem Cell Transplantation From a Haploidentical Family Donor Compared to Post-transplant Cyclophosphamide in Patients With Blood Cancer

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE III, RANDOMIZED CONTROLLED STUDY TO COMPARE SAFETY AND EFFICACY OF A HAPLOIDENTICAL HSCT AND ADJUNCTIVE TREATMENT WITH ATIR101 VERSUS A HAPLOIDENTICAL HSCT WITH POST-TRANSPLANT CYCLOPHOSPHAMIDE IN PATIENTS WITH HEMATOLOGIC MALIGNANCY

Intervention/treatment:
ATIR101 / ANTI-THYMOCYTE GLOBULIN (RABBIT) / FLUDARABINE PHOSPHATE / MELPHALAN HCL / RITUXIMAB / THIOTEPA / CYCLOPHOSPHAMIDE
Medical condition:
HEMATOLOGICAL MALIGNANCIES
Protocol code:
CR-AIR-009
Control number:
200672
Status:
Closed
Approved:
January 06, 2017
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02999854
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 70 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Klaudia Traudtner, MD. Head of Safety and Pharmacovigilance.
Organization
Kiadis Pharma Netherlands B.V
Phone:
+31 (0)20 240 52 50
Sponsor
KIADIS PHARMA NETHERLANDS BV

Locations

Quebec

Maisonneuve-Rosemont Hospital
Montreal, Quebec, H1T 2M4

Results

See the results from the trial NCT02999854. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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