Small molecule · Inhibitor of PI3K class I and histone deacetylase · developed by Curis
Fimepinostat is an orally bioavailable inhibitor of phosphoinositide 3-kinase (PI3K) class I and pan histone deacetylase (HDAC) enzymes. It prevents activation of the PI3K-AKT-mTOR pathway and induces apoptosis in tumor cells. It is studied in relapsed and/or refractory lymphomas including diffuse large B-cell lymphoma.
Summary written with AI from the sources listed at the end of this page.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT02674750 | Phase 2 | Relapsed and/or Refractory Diffuse Large B-cell Lymphoma Including With Myc… | Completed | CRIS |
| NCT01742988 | Phase 1 | Lymphoma | Completed | CRIS |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Double-expressor Lymphoma (DEL)Double-hit Lymphoma (DHL)High-grade B-cell Lymphoma (HGBL)LymphomaRefractory Diffuse Large B-Cell Lymphoma (DLBCL)Refractory LymphomaRelapsed and/or Refractory LymphomaRelapsed Ddiffuse Large B-Cell Lymphoma (DLBCL)Relapsed LymphomaTriple-hit Lymphoma (THL)
See CRIS's upcoming FDA decisions, trial readouts, cash runway and dilution risk, updated every day from SEC, FDA and ClinicalTrials.gov filings.
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