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Clinical Trial Summary

To ascertain the safety and efficacy of Istodax® in actual clinical settings in patients with relapsed or refractory peripheral T-cell lymphoma (PTCL) who receive Istodax. 1. Planned registration period 4 years 2. Planned surveillance period 5 years and 6 months


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03742921
Study type Observational
Source Celgene
Contact
Status Completed
Phase
Start date February 4, 2019
Completion date October 31, 2023

See also
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