Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in

Clinical Trial Summary

The purpose of this open label study is to determine whether combining pracinostat (study drug) with Vidaza (azacitidine) or Dacogen (decitabine) will improve clinical responses in Myelodysplastic Syndrome (MDS) patients who have failed an initial single agent hypomethylating agent (HMA), and to provide additional safety and efficacy data.

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NCT number	NCT01993641
Study type	Interventional
Source	Helsinn Healthcare SA
Contact
Status	Completed
Phase	Phase 2
Start date	December 2013
Completion date	June 2016

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA — MEI-005

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms