Solid Tumors Clinical Trial
Official title:
Phase I Open Label, Multi-center Study to Assess the Safety, Tolerability and Pharmacokinetics of Orally Administered CUDC-907, an HDAC and PI3K Inhibitor, in Subjects With Advanced/Relapsed Solid Tumors
This is a Phase I, open-label, multi-center trial designed to evaluate the safety, tolerability and pharmacokinetics of CUDC-907 administered orally to subjects with advanced/relapsed solid tumors.
This is a Phase I, open-label, multi-center trial designed to evaluate the safety,
tolerability and pharmacokinetics of CUDC-907 administered orally to subjects with
advanced/relapsed solid tumors. The following dosing schedule, consisting of 21-day treatment
cycles, is being examined:
Five days on/two days off on Days 1 to 5, 8 to 12, and 15 to 19 (5/2 schedule).
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Active, not recruiting |
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