A Pharmacokinetic (PK) Study of Nilotinib in Pediatric Patients With Philadelphia Chromosome-positive (Ph+) Chronic Myelogenous Leukemia (CML) or Acute Lymphoblastic Leukemia (ALL)

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

April 14, 2011

Primary Completion Date

July 1, 2015

Study Completion Date

July 1, 2015

Conditions
Chronic Myeloid LeukemiaAcute Lymphoblastic Leukemia
Interventions
DRUG

Nilotinib

"Nilotinib capsules were delivered in bottles with dose strengths of 50mg, 150mg and 200mg.~Patients were administered nilotinib 230 mg/m2 (per BSA) bid, orally, rounded to the nearest 50 mg (max single dose 400 mg) for 28 days (1 cycle) for up to 12 cycles prior to protocol amendment 3 and up to 24 cycles post amendment 3. Capsules were to be swallowed whole with water. Apple sauce (puréed apple) may have been used as a vehicle for dosing where capsules were not able to be swallowed whole with water."

Trial Locations (12)

20900

Novartis Investigative Site, Monza

33076

Novartis Investigative Site, Bordeaux

35128

Novartis Investigative Site, Padua

59037

Novartis Investigative Site, Lille

75571

Novartis Investigative Site, Paris

86021

Novartis Investigative Site, Poitiers

00161

Novartis Investigative Site, Roma

1081 HV

Novartis Investigative Site, Amsterdam

3015 CN

Novartis Investigative Site, Rotterdam

B4 6NH

Novartis Investigative Site, West Midlands

SM2 5PT

Novartis Investigative Site, Sutton

BS2 8BJ

Novartis Investigative Site, Bristol

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY