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Clinical Trial Summary

This study evaluated the safety and tolerability of using HSC835 in patients with hematological malignancies.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Acute Lymphocytic Leukemia
  • Acute Myelocytic Leukemia
  • Burkitt Lymphoma
  • Burkitt's Lymphoma
  • Chronic Lymphocytic Leukemia
  • Chronic Myelogenous Leukemia
  • Follicular Lymphomas
  • Hematologic Neoplasms
  • High Grade Lymphomas
  • Large-cell Lymphoma
  • Leukemia
  • Leukemia, Lymphocytic, Chronic, B-Cell
  • Leukemia, Lymphoid
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Leukemia, Myeloid
  • Leukemia, Myeloid, Acute
  • Lymphoblastic Lymphoma
  • Lymphoma
  • Lymphoma, Mantle-Cell
  • Lymphoma, Non-Hodgkin
  • Lymphoplasmacytic Lymphoma
  • Mantle-cell Lymphoma
  • Marginal Zone Lymphoma
  • Myelodysplastic Syndrome
  • Myelodysplastic Syndromes
  • Neoplasms
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Waldenstrom Macroglobulinemia

NCT number NCT01474681
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 1/Phase 2
Start date January 9, 2012
Completion date October 3, 2016

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