Overview
Dose Escalation Study of NKP-1339 to Treat Advanced Solid Tumors
Status:
Completed
Completed
Trial end date:
2016-01-01
2016-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine the safety and maximal tolerated dose of NKP-1339, a ruthenium containing compound administered intravenously on a weekly schedule, in patients with advanced solid tumors. The responses to treatment in this population will be evaluated. In addition, the PD and PK properties of the compound will be explored.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Niiki Pharma Inc.
Criteria
Inclusion Criteria:- Patients ≥ 18 years with histologically or cytologically confirmed advanced solid
tumors refractory to standard therapies who have signed an IRB approved Informed
Consent Form (ICF).
- ECOG PS 0 or 1.
- Adequate hematologic, hepatic and renal function
- Minimum life expectancy ≥ 12 weeks
Exclusion Criteria:
- No supplemental Iron, i.e., therapeutic or as part of a multivitamin regimen.
- No chemotherapy, immunotherapy, or radiotherapy for < 4 weeks, BMTs < 9 months or
major surgery < 3 weeks.
- No symptomatic central nervous system metastases. No primary brain tumors or known
brain metastasis unless clinically stable and on stable or reducing dose of steroids.
- No evidence of ischemia, MI within the past 6 months, or other significant abnormality
on ECG.
- No clinically significant active infection including HIV, hepatitis B, or hepatitis C.
- No Peripheral neuropathy ≥ Grade 2