Disease |
Protocol |
Description |
| Anal
Cancer |
|
RT + 5-FU +
Mito-C vs. RT + 5-FU + CDDP
|
| Bile Duct Cancer |
|
Phase II Rebeccamycin
|
| Colon/Rectal
Cancer |
|
Phase II study
of oral Xeloda in combination with intravenous Irinotecan
|
| Colon/Rectal Cancer |
UAB
0237 |
Phase II multicenter
study of Erbitux™ (Cetuximab) in patients with metastatic
colorectal carcinoma
|
| Colon/Rectal Cancer |
|
Phase II study
safety and immunogenicity of ALVAC-CEA/B7.1 vaccine
|
| Colon/Rectal Cancer |
UAB
0249 |
A feasibility
study of Oxaliplatin in combination with an infusional or
weekly bolus 5-FU/LV or Capecitabine as first line treatment
of patients with advanced colorectal cancer
|
| Colon/Rectal Cancer |
ECOG
N9841 |
Randomized
Phase II equivalence trial of Irinotecan vs. Oxaliplatin
in combination with an infusional or weekly bolus 5-FU/LV
or Capecitabine as first line treatment of patients with
advanced colorectal cancer
|
| Colon/Rectal Cancer |
|
Phase IIB evaluation
of Cyclooxygenase-2 activity in surgically resected primary
colorectal adenomas and carcinomas after 7 days pretreatment
with Celecoxib
|
| Esophageal
Cancer |
|
A Phase II
study of Irinotecan and Taxotere with concurrent radiotherapy
as a preoperative treatment in resectable esophageal cancer
|
Gallbladder
Cancer
|
|
Phase II Rebeccamycin |
| Liver Cancer |
|
A Phase I/II
open label study of T138057-sodium in patients with advanced,
surgically unresectable hepatocellular carcinoma
|
| Liver Cancer |
|
Phase II Rebeccamycin
|
| Pancreatic Cancer |
UAB
0105 |
Phase III PN-401
with High Dose 5FU vs. Gemcitabine
|
| Pancreatic
Cancer |
|
Phase I/II open
label study of Capecitabine with concurrent radiotherapy
|
| Pancreatic Cancer |
UAB
0243 |
Randomized,
placebo-controlled, double blind Phase II study of Gemcitabine
+ Ly293111 compared to Gemcitabine + placebo in patients
with locally advanced or metastatic pancreatic cancer
|
| All cancers may
be elligible |
|
Phase I DX-8951f
in patients with liver dysfunction
|
| All cancers may
be elligible |
|
Phase I DX-891f
in patients with renal dysfunction
|