WHO ICTRP trial

A comparison of two low-intensity transplant regimens for the treatment of…

EUCTR2017-004800-23-GB · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2017-004800-23-GB
Public title A comparison of two low-intensity transplant regimens for the treatment of adults with acute lymphoblastic leukaemia (ALL) over the age of 40 years (ALL-RIC)
Scientific title A comparison of reduced dose total body irradiation (TBI) and cyclophosphamide with fludarabine and melphalan reduced intensity conditioning in adults with acute lymphoblastic leukaemia (ALL) in complete remission. - ALL-RIC
Primary sponsor University of Birmingham
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries United Kingdom
Conditions Acute Lymphoblastic Leukaemia (ALL) MedDRA version: 20.1 Level: LLT Classification code 10000844 Term: Acute lymphoblastic leukaemia System Organ Class: 100000004864 ;Therapeutic area: Diseases [C] - Cancer [C04]
Interventions Product Name: Cyclophosphamide Product Code: Cyclophosphamide Pharmaceutical Form: Powder for solution for infusion INN or Proposed INN: cyclophosphamide CAS Number: 50-18-0 Current Sponsor code: Cyclophosphamide Concentration unit: mg/kg…
Registration date Feb 8, 2018
Target size 242
Secondary IDs RG-17-241
Registry page clinicaltrialsregister.eu

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