www.virginiacancer.com ~ site index
Virginia Oncology Associates
Clinical Research Program Trials and Eligibility
Medical
Oncologists
Medical Oncology is a service provided by a team that consists of Medical Oncologists and Oncology Nurses.
Gynecologic
Oncologists
Doctors specializing in the study & treatment of malignancies arising in the female reproductive tract.
 
 
About VOA
Notice of Privacy Practices
Medical Oncologists
Gynecologic Oncologists
Radiation Oncologists
Office Locations
Locations Map
Health Plans
Awards & Accreditations
 
 
Medical Oncology
Gynecological Oncology
Clinical Research Programs
Phase I Clinical Research Programs
Hematology

Stem Cell Transplant
Clinical Laboratory
Pharmacy
Nuclear Medicine
Radiation Oncology
Ultrasound
Bone Density
Genetic Counseling
 
 
Physician Lectures
Physician Resources
 
 
Support Groups
Support Resources
Education
News and Events
 
 
Comprehensive Cancer Care
Legis Link
 
 
Contact Information
Office Locations
Careers
Press Releases

 



If you are interested in learning more about our research program, please call the
VOA Research Department
(757) 466-8683 (Southside) or (757) 873-9833 (Peninsula).

PHASE I STUDIES

USO 05-033: A Phase I Open Label, Multicenter, Dose-Escalation Study to Determine the Maximum Tolerated Dose (MTD), Dose Limiting Toxicity (DLT), Safety and Pharmacokinetics of CGC-11047 when used in individual combinations with Gemcitabine or 2) Docetaxel or 3) Bevacizumab or 4) Erlotinib in patients with advanced solid tumors or lymphoma.

USO 05-125: Phase I Dose-Escalation Study of Seneca Valley Virus (SVV-001), a Replication-Competent Picornavirus, in patients with advanced solid tumors with neuroendocrine features

USO 05-038: A Phase I Trial of Imexon, Injection plus Gemcitabine in advanced, previously untreated pancreatic adenocarcinoma.

USO 05-033: A Phase I Open Label, Multicenter, Dese-Escalation Study to determine the maximum tolerated dose (MTD), Dose Limiting Toxicity (DLT), Safety and Pharmacokinetics of CGC-11047 when used in individual combinations with 1) Gemcitabine or 2) Docetaxel or 3) Bevacizumab or 4) Erlotinib in patients with advanced solid tumors or lymphoma.

USO 05-146: A Phase I Open Label Dose Escalation Study of Continuous Oral Treatment with BIBF 1120 ES Together with Paclitaxel and Carboplatin in patients with advanced stage non-small-cell lung cancer.

USO 05-012: A Phase I, Open-Label, Dose Escalation Study of Weekly Dosing with BB-10901, followed by a phase II Efficacy Expansion.

© Virginia Oncology Associates 2005 - Affiliate of US Oncology
Lake Wright Cancer Center 5900 Lake Wright Drive, Norfolk Virginia 23502 Central Business Office: (757)466-8683 Visionefx