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Study of SyB C-1101 in Patients With Myelodysplastic Syndrome

Myelodysplastic Syndrome Clinical Trial

Official title:
Multi-center, Open-label, Phase I Study of SyB C-1101 in Patients With Myelodysplastic Syndrome

Clinical Trial Summary

To assess tolerability of SyB C-1101 when administered orally BID for 21 days followed by a 7-day observation period in patients with recurrent/relapsed or refractory myelodysplastic syndrome in order to determine a recommended dose (RD). To assess safety, efficacy and pharmacokinetics.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03495167
Study type Interventional
Source SymBio Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date October 6, 2017
Completion date May 28, 2019
View Details
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