Clinical Trial Detail


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NCT ID NCT01177397
Title Study to Assess Safety, Pharmacokinetics, and Efficacy of Oral CC-223 for Patients With Advanced Solid Tumors, Non-Hodgkin Lymphoma or Multiple Myeloma
Recruitment Completed
Gender both
Phase Phase Ib/II
Variant Requirements No
Sponsors Celgene Corporation

estrogen-receptor positive breast cancer

neuroendocrine tumor

progesterone-receptor positive breast cancer

hepatocellular carcinoma


diffuse large B-cell lymphoma

Advanced Solid Tumor

multiple myeloma

Her2-receptor positive breast cancer

lung non-small cell carcinoma



Age Groups: adult | senior
Covered Countries USA | FRA | ESP

No variant requirements are available.