CompletedPhase 1NCT02358395

A Study of BBI608 Administrated With Sorafenib in Adult Patients With Advanced Hepatocellular Carcinoma

Studying Adult hepatocellular carcinoma

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Key facts

Sponsor
Sumitomo Pharma Co., Ltd.
Principal Investigator
Director, Drug Development Division
Sumitomo Pharma Co., Ltd.
Intervention
BBI608(drug)
Enrollment
12 enrolled
Eligibility
20 years · All sexes
Timeline
20152017

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT02358395 on ClinicalTrials.gov

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