Study #2018-1160
A Phase I, Multi-Center, Open-Label Study To Assess The Safety, Pharmacokinetics, And Preliminary Efficacy Of An Orally Available Small Molecule, Cc-99282, Alone And In Combination With Anti-Lymphoma Agent In Subjects With Relapsed Or Refractory Non-Hodgk
MD Anderson Study Status
Enrolling
Treatment Agent
CC-99282, Rituximab, Obinutuzumab, Tafasitamab, Tazemetostat
Description
The purpose of this study is to evaluate the safety, tolerability, and preliminary efficacy of CC-99282 alone and in combination with anti-lymphoma agents in participants with relapsed or refractory non-Hodgkin's lymphomas.
Information and next steps
Disease:
Lymphoma, Non-Hodgkin
Study phase:
I
Physician name:
Loretta Nastoupil
Department:
Lymphoma/Myeloma
For general questions about clinical trials:
1-877-632-6789
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