Study #2021-0111
A Phase 1, Multicenter, Open-Label, Dose Finding Study of CC-96673 in Subjects with Relapsed or Refractory Non-Hodgkin's Lymphoma
MD Anderson Study Status
Enrolling
Treatment Agent
CC-96673
Description
The purpose of this Phase 1 study is to evaluate the safety and tolerability of CC-96673 in adult participants with Relapsed or Refractory Non-Hodgkin's Lymphoma (R/R NHL). The study will be conducted in 2 parts: Part A, monotherapy dose escalation and Part B, monotherapy dose expansion. Parts A and B will consist of 3 periods: Screening, Treatment, and Follow-up.
Information and next steps
Disease:
Lymphoma, Non-Hodgkin
Study phase:
I
Physician name:
Paolo Strati
Department:
Lymphoma/Myeloma
For general questions about clinical trials:
1-877-632-6789
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