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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Page 1 of 3 (10 locations)

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