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Metadata

Name
Study to Assess the Safety, Tolerability and Pharmacokinetics of Fimepinostat (CUDC-907) in Patients With Lymphoma
Repository
ClinicalTrials.gov
Identifier
clinicaltrials:NCT01742988
Description
This is a phase 1, open-label, dose-escalation study of fimepinostat (CUDC-907) in patients
with relapsed and/or refractory diffuse large B-cell lymphoma (DLBCL), or high-grade B-cell
lymphoma (HGBL) with or without MYC and BCL2 alterations. Fimepinostat (CUDC-907) is a
multi-targeted agent designed to inhibit phosphoinositide 3-kinase (PI3K)and histone
deacetylase (HDAC). The study is designed to assess the safety, the maximum tolerated dose,
the recommended phase 2 dose (RP2D), pharmacokinetics and the anti-cancer activity of oral
fimepinostat in combination with 1 or more anti-cancer regimens.
Data or Study Types
clinical trial
Keywords
Triple-hit Lymphoma (THL), HGBL, Double-expressor Lymphoma (DEL), P13K, Open-Label, Diffuse Large B-Cell Lymphoma, HDAC, MYC, Double-hit Lymphoma (DHL), Lymphoma, DLBCL, High-grade B-Cell Lymphoma
Source Organization
Unknown
Access Conditions
available
Year
2012
Access Hyperlink
https://clinicaltrials.gov/ct2/show/NCT01742988

Distributions

  • Encoding Format: HTML ; URL: https://clinicaltrials.gov/ct2/show/results/NCT01742988
This project was funded in part by grant U24AI117966 from the NIH National Institute of Allergy and Infectious Diseases as part of the Big Data to Knowledge program. We thank all members of the bioCADDIE community for their valuable input on the overall project.