UPCC 06419: Phase 1/2 Open Label Multi-center Dose-Escalation Study to Assess the Safety Tolerability and Pharmacokinetics of Orally Administered Fimepinostat (CUDC-907) a PI3K and HDAC Inhibitor in Subjects with Relapsed and/or Refractory Lymphoma
Recruiting
99 years or below
All
Phase
1
1 Location
Brief description of study
This is a Phase 1/2, open-label, multicenter dose-escalation and dose-expansion trial evaluating the safety and tolerability of fimepinostat administered orally to patients with R/R lymphoma.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: lymphoma
-
Age: 99 years or below
-
Gender: All
Updated on
19 Feb 2024.
Study ID: 832894