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Phase 1 Trial of CUDC-907

Phase 1 Trial of CUDC-907

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This study is now recruiting. Learn more about enrolling here.

Description

This study involves taking a study drug called CUDC-907.  CUDC-907 is an oral drug that blocks certainproteins in tumor cells; these proteins may be important in the growth of somecancers. The overall goals of this study are to evaluate the side effects andbenefits of CUDC-907 in patients with relapsed or treatment refractory solidtumor, brain tumor, or lymphoma, and to determine the best dose of CUDC-907 forchildren and adolescents.  This studywill also look at the levels of CUDC-907 in the blood over time after a dose. 

Eligibility and criteria


IRB Number:
16-013562
Eligible age range:
1 years - 21 years
Clinical trial phase:
Phase I
Official title:
Phase 1 Trial of CUDC-907 in Children and Young Adults with Relapsed or Refractory Solid Tumors, CNS Tumors, or Lymphoma

What to expect

This study will enroll male and female patients who are between 1 and 21years of age and who have relapsed or refractory solid tumor, brain tumor, orlymphoma. Subjects will take CUDC-907 capsules by mouth. CUDC-907 must be taken within 30 minutes of ameal. Subjects will be asked to keep a drug diary and write down informationabout the study drug.  

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Your time and participation make a difference in supporting the work of the Research Institute and children in our community. Learn more about opportunities to participate in our research.

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