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Clinical Trial Summary

- To investigate the safety and tolerability of OPB-31121 following repeated oral administration of OPB-31121 in patients Non-Hodgkin's Lymphoma(NHL) or Multiple Myeloma(MM)

- To determine the potential dose-limiting toxicities and maximum-tolerated dose in patients treated with OPB-31121

- To determine the pharmacokinetics and anti-tumor efficacy of OPB-31121 in patients


Clinical Trial Description

The study is designed as a single-center,open-label,phase 1 dose-escalation study to assess the safety,tolerability,pharmacokinetics, and anti-tumor efficacy of OPB-31121 in patients with relapsed or refractory NHL or MM.

- To investigate the safety and tolerability of OPB-31121 following repeated oral administration of OPB-31121 in patients NHL or MM

- To determine the potential dose-limiting toxicities and maximum-tolerated dose in patients treated with OPB-31121

- To determine the pharmacokinetics and anti-tumor efficacy of OPB-31121 in patients ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00511082
Study type Interventional
Source Otsuka Beijing Research Institute
Contact Shii Man, M.D & Ph.D.
Phone +86-10-85182966
Email mans@obri.otsuka.com
Status Unknown status
Phase Phase 1
Start date December 2007
Completion date December 2009

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05439538 - Serum NGAL IN Patients With Multiple Myeloma