Safety and Efficacy of LEE011 and LGX818 in Patients With BRAF Mutant Melanoma.

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

July 31, 2013

Primary Completion Date

April 30, 2015

Study Completion Date

April 30, 2015

Conditions
Locally Advanced Metastatic BRAF Mutant Melanoma
Interventions
DRUG

LEE011

LEE011 will be administered orally, once daily for 21 consecutive days followed by a 7-day planned break (28-day cycle).

DRUG

LGX818

LGX818 will be administered orally, once daily on a continuous dosing schedule (28-day cycle).

Trial Locations (9)

2145

Novartis Investigative Site, Westmead

5011

Novartis Investigative Site, Woodville

37232

Vanderbilt University Medical Center SC - Dept of Oncology ., Nashville

48201

Karmanos Cancer Institute Dept of Oncology, Detroit

80045

University of Colorado Dept of Oncology, Aurora

90033

Memorial Sloan Kettering Cancer Center Dept Oncology, New York

97239

Oregon Health & Science University Dept. of OHSU (3), Portland

H2X 3J4

Novartis Investigative Site, Montreal

3584CX

Novartis Investigative Site, Utrecht

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Array BioPharma

INDUSTRY