| Protocol Number |
Study Title |
|
CALGB 70305 |
A Randomized Study to Prevent Lymphedema in Women Treated for Breast Cancer |
|
CALGB 70501 |
Collection of Patient-Reported Symptoms and Performance Status via the Internet
|
|
CALGB 70604 |
A Randomized, Phase III Study of Standard Dosing versus Longer Dosing
Interval of Zoledronic Acid in Metastatic Cancer
|
|
CALGB 80302 |
A Phase II Trial of Preoperative Irinotean, Cisplatin and Radiation in Esophageal Cancer |
|
CALGB 80403 |
Randomized Phase II Study of ECF-C, IC-C or FOLFOX-C in Metastatic Esophageal and GE Junction Cancer
|
|
CALGB 80405 |
A Phase III Trial of Irinotecan/5-FU/
Leucovorin or Oxaliplatin/5-FU/Leucovorin with Bevacizumab, or Cetuximab (C225), or with the Combination of Bevacizumab and Cetuximab for Patients with Untreated Metastatic Adenocarcinoma of the Colon or Rectum |
|
CALGB 80702 |
A Phase III Trial of 6 versus 12 Treatments of Adjuvant FOLFOX plus Celecoxib or Placebo for Patients with Resected Stage III Colon Cancer
|
|
CALGB 80802 |
Phase III Randomized Study of Sorafenib plus Doxorubicin versus Sorafenib in Patients with Advanced Hepatocellular Carcinoma (Hcc) |
|
CALGB 8461 |
CYTOGENETIC STUDIES IN ACUTE LEUKEMIA |
|
CALGB 90202 |
A Randomized, Double-Blind, Placebo-Controlled Phase III Study of Early versus Standard Zoledronic Acid to Prevent Skeletal Related Events in Men with Prostate Cancer Metastatic to Bone |
|
CALGB 90203 |
Randomized Phase III Study of Neo-Adjuvant Docetaxel and Androgen Deprivation Prior to Radical Prostatectomy versus Immediate Radical Prostatectomy in Patients with High-Risk, Clinically Localized Prostate Cancer |
|
CALGB 90601 |
A Randomized Double-Blinded Phase III Study Comparing Gemcitabine, Cisplatin, and Bevacizumab to Gemcitabine, Cisplatin, and Placebo in Patients with Advanced Transitional Cell Carcinoma |
|
CALGB 9665 |
THE CALGB LEUKEMIA TISSUE BANK
|
|
CCCWFU 91105 |
Phase III Double Blind, Placebo Controlled Study of Donepezil in the Irradiated Brain
|
|
CCCWFU 97202 |
A Randomized Double-Blind Placebo-Controlled Study of Oral Coenzyme Q10 to Relieve Self-Reported Cancer Treatment Related Fatigue in
Breast Cancer Patients
|
|
CCCWFU 97509 |
A Phase II Double-Blind Feasibility Study of Armodafinil for Brain Radiation-Induced Fatigue
|
|
Co-STAR |
(Breast Cancer Prevention)
Effects of Selective Estrogen Receptor Modulators on Cognitive Aging: Cognition in the Study of Tamoxifen and Raloxifene (Co-STAR) |
|
CTSU 25-02 |
Tamoxifen and Exemestane Trial (TEXT)
A Phase III Trial Evaluating the Role of Exemestane Plus GnRH Analogue as Adjuvant Therapy for Premenopausal Women with Endocrine Responsive Breast Cancer
Ovarian function suppression + tamoxifen versus
Ovarian function suppression + exemestane |
|
CTSU E1208 |
A Phase III Randomized Trial of Chemoembolization with or without Sorafenib in Unresectable Hepatocellular Carcinoma (HCC) in Patients with and without Vascular Invasion |
|
CTSU E1305 |
A Phase III Randomized Trial of Chemotherapy with or without Bevacizumab in Patients with Recurrent or Metastatic Head and Neck Cancer |
|
CTSU E1505 |
A Phase III Randomized Trial of Adjuvant Chemotherapy With or Without Bevacizumab for Patients With Completely Resected Stage IB (> 4 cm) -IIIA Non-Small Cell Lung Cancer (NSCLC) |
|
CTSU E1697 |
Phase III Randomized Study of Four Weeks High Dose IFN-α2b in Stage T2b No, T3a-bN0, T4a-b No, and T1-4, N1a, 2a (microscopic) Melanoma
|
|
CTSU E1A06 |
An Intergroup Phase III Randomized Controlled Trial Comparing Melphalan, Prednisone and Thalidomide Versus Melphalan, Prednisone and Lenalidomide in Newly Diagnosed Myeloma Patients Who Are Not Candidates for High-Dose Therapy |
|
CTSU E2804 |
The BeST Trial: A Randomized Phase II Study of VEGF, RAF kinase, and mTOR Combination Targeted Therapy (CTT) with Bevacizumab, Sorafenib and Temsirolimus in Advanced Renal Cell Carcinoma
|
|
CTSU E2905 |
Randomized Phase III Trial Comparing the Frequency of Major Erythroid Response (MER) to Treatment with Lenalidomide (Revlimid®) Alone and in Combination with Epoetin Alfa(Procrit®) in Subjects with Low- or Intermediate-1 Risk MDS and Symptomatic Anemia |