A Dose-Escalation Study of OBP-801 in Patients With Advanced Solid Tumors
| Status: | Active, not recruiting | 
|---|---|
| Conditions: | Cancer | 
| Therapuetic Areas: | Oncology | 
| Healthy: | No | 
| Age Range: | 18 - Any | 
| Updated: | 3/15/2019 | 
| Start Date: | March 2015 | 
| End Date: | August 2019 | 
A Phase 1a Dose-Escalation Study of OBP-801 in Patients With Advanced Solid Tumors
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.
			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.
We found this trial at
    1
    site
	
		Barbara Ann Karmanos Cancer Institute Karmanos is based in southeast Michigan, in midtown Detroit, and...  
  
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