Status:
COMPLETED
Dose Escalation Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous ALN-VSP02 In Patients With Advanced Solid Tumors With Liver Involvement
Lead Sponsor:
Alnylam Pharmaceuticals
Conditions:
Solid Tumors
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The purpose of the study is to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics of intravenous ALN-VSP02, an RNAi therapeutic, in patients with advanced solid tumors with liv...
Eligibility Criteria
Inclusion
- Patients must have histologically or cytologically confirmed advanced solid tumors that have recurred or progressed following standard therapy, or that have not responded to standard therapy, or for which there is no standard therapy, or who are not candidates for standard therapy
- Patient has measurable tumor in the liver
- At least 28 days have elapsed since the patient's prior systemic therapy, radiotherapy, or any major surgery
- Patient has an Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1
- Patient has adequate hematologic, liver, and renal function
- Patient is seronegative for hepatitis B virus (HBV) and hepatitis C virus (HCV)
- Patient has a life expectancy \> 12 weeks
Exclusion
- Patient is receiving full-dose (therapeutic) anticoagulation therapy and/or aspirin \> 325 mg/day or other platelet inhibitory agents
- Patient has clinically significant cardiovascular disease or uncontrolled serious cardiac arrythmia
- Patient has known active brain or leptomeningeal metastases
- Patient has clinically significant cerebrovascular disease
- Patient has a seizure disorder not controlled on medication
- Patient has a known or suspected viral, parasitic or fungal infection
- Patient previously experienced a severe reaction to a liposomal product
- Patient has a known hypersensitivity to lipid products
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2011
Estimated Enrollment :
41 Patients enrolled
Trial Details
Trial ID
NCT00882180
Start Date
March 1 2009
End Date
August 1 2011
Last Update
August 24 2011
Active Locations (10)
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1
TGen Clinical Research Service at Scottsdale Healthcare
Scottsdale, Arizona, United States, 85258
2
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
3
Dana Farber Cancer Institute
Boston, Massachusetts, United States, 02115
4
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215