WHO ICTRP trial

A trial to test if decitabine can be used to treat patients with Myelodysplastic…

EUCTR2009-017098-40-GB · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2009-017098-40-GB
Public title A trial to test if decitabine can be used to treat patients with Myelodysplastic Syndrome (MDS) that have already been treated with Azacitidine (AZA)
Scientific title Use of Decitabine in Myelodysplastic Syndrome (MDS) Following Azacitidine (AZA) Failure (DEC-MDS) - DEC-MDS
Primary sponsor King's College London
Secondary sponsors King's College Hospital NHS Foundation Trust
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
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 Myelodysplastic Syndromes Acute Myeloid Leukaemia Chronic Myelomonocytic Leukaemia MedDRA version: 14.1 Level: LLT Classification code 10054350 Term: Chronic myelomonocytic leukemia System Organ Class: 10029104 - Neoplasms benign, malignant…
Interventions Trade Name: Dacogen Product Name: DECITABINE Pharmaceutical Form: Powder for solution for infusion INN or Proposed INN: DACOGEN CAS Number: 2353-33-5 Concentration unit: mg/m2 milligram(s)/square meter Concentration type: equal…
Registration date Jun 29, 2010
Target size 50
Secondary IDs DEC-MDS
Registry page clinicaltrialsregister.eu

At a glance

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