Study of Efficacy and Safety of LDE225 in Adult Patients With Relapsed/Refractory Acute Leukemia

PHASE2CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

May 31, 2013

Primary Completion Date

May 31, 2015

Study Completion Date

May 31, 2015

Conditions
Acute Leukemias
Interventions
DRUG

LDE225

LDE225 will be supplied as 200 mg capsules by Novartis. Patients will receive study treatment on an outpatient basis. LDE225 will be dispensed every two weeks for the first four weeks and at the start of every four weeks thereafter, as needed.

Trial Locations (23)

1090

Novartis Investigative Site, Vienna

3000

Novartis Investigative Site, Leuven

3181

Novartis Investigative Site, Prahran

4032

Novartis Investigative Site, Debrecen

5000

Novartis Investigative Site, Adelaide

5020

Novartis Investigative Site, Salzburg

5530

Novartis Investigative Site, Yvoir

7006

Novartis Investigative Site, Trondheim

27710

Duke University Medical Center SC-5, Durham

37007

Novartis Investigative Site, Salamanca

39120

Novartis Investigative Site, Magdeburg

46026

Novartis Investigative Site, Valencia

60590

Novartis Investigative Site, Frankfurt

89081

Novartis Investigative Site, Ulm

H1T 2M4

Novartis Investigative Site, Montreal

H3T 1E2

Novartis Investigative Site, Montreal

01307

Novartis Investigative Site, Dresden

1081 HV

Novartis Investigative Site, Amsterdam

6525 GA

Novartis Investigative Site, Nijmegen

3015 CE

Novartis Investigative Site, Rotterdam

3075 EA

Novartis Investigative Site, Rotterdam

NO-5021

Novartis Investigative Site, Bergen

WC1E 6HX

Novartis Investigative Site, London

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY