Detroit, Michigan 48201


This Phase 1a, single center, open-label, repeat dose study will evaluate the safety, efficacy, and Pharmacokinetics of ascending doses of OBP-801 in patients with advanced solid tumors.


Patient Inclusion Criteria Patients must meet all of the following inclusion criteria to be eligible for enrollment into the study: - Histologically or cytologically confirmed metastatic or unresectable solid tumor. - Has failed treatment with all standard therapies for their malignancy. - Adequate Karnofsky Performance Status. - An expected survival of at least 3 months. - Adequate organ and bone marrow function. - Signed informed consent form for study participation prior to screening. Patient Exclusion Criteria Patients presenting with any of the following will be excluded in the study: - Clinically significant disease as defined by the protocol. - Surgical therapy or other therapies within period as defined by the protocol. - Any condition that will interfere with compliance with the protocol as determined by investigator.



Primary Contact:

Makoto Seki, Ph.D.
Phone: 81-3-5472-1578

Backup Contact:


Location Contact:

Detroit, Michigan 48201
United States

Clinical Trials Office
Phone: 800-527-6266

Site Status: Recruiting

Data Source:

Date Processed: June 25, 2018

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