Safety and Tolerability of HSC835 in Patients With Hematological Malignancies

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

January 9, 2012

Primary Completion Date

October 3, 2016

Study Completion Date

October 3, 2016

Conditions
Acute Myelocytic LeukemiaAcute Lymphocytic LeukemiaChronic Myelogenous LeukemiaMyelodysplastic SyndromeChronic Lymphocytic LeukemiaMarginal Zone LymphomaFollicular LymphomasLarge-cell LymphomaLymphoblastic LymphomaBurkitt's LymphomaHigh Grade LymphomasMantle-cell LymphomaLymphoplasmacytic Lymphoma
Interventions
BIOLOGICAL

HSC835

Trial Locations (1)

55455

Novartis Investigative Site, Minneapolis

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY