7
Participants
Start Date
January 31, 2015
Primary Completion Date
October 31, 2015
Study Completion Date
October 31, 2015
LDE225
"Lead-In: LDE225 will be administered orally at three dose levels starting at 400mg. If acceptable tolerability is demonstrated, escalations may continue up to 800 mg. LDE225 will be administered orally as a single daily dose for 21 days in combination with a fixed dose of bortezomib to be given on Days 1, 4, 8, 11 of each 21 day cycle.~Dose Expansion: LDE225 will be given as a single oral daily dose for 21 days at the MTD determined in the lead-in phase.~Maintenance Therapy: Patients who complete 16 cycles of therapy with stable disease or better will be eligible for single agent maintenance therapy of LDE225 at the MTD orally for up to 2 years or until progressive disease or unacceptable toxicity."
Bortezomib
In both the lead-in and dose expansion portions of the study, bortezomib, 1.3 mg/m2, will be administered by subcutaneous injection (SQ) on Days 1, 4, 8, 11 of each 21 day cycle.
Tennessee Oncology PLLC, Nashville
Tennessee Oncology, Chattanooga
Oncology Hematology Care, Cincinnati
Texas Transplant Institute/Methodist Healthcare, San Antonio
Colorado Blood Cancer Institute, Denver
Collaborators (1)
Novartis
INDUSTRY
SCRI Development Innovations, LLC
OTHER