Priority Lists
Protocol Posting of
Activations
Closures
Permanent Closure Effective 1/8/02
A Phase III Study of Doxorubicin-Cyclophosphamide Therapy Followed by Paciltaxel or Docetaxel Given Weekly or Every 3 Weeks in Patients with Axillary Node-Positive or High-Risk Node Negative Breast Cancer
Study Coordinator(s) | Silvana Martino, D.O. |
Participants | Members, Medical Oncologists, Pathologists, NCORP, Surgeons |
Closure Date | 2002-01-08 |
Temporary Closure effective 2/1/02
A Phase II Study of Gemcitabine Plus Irinotecan (CPT-11) In Patients With Esophageal Cancer.
Study Coordinator(s) | Stephen K. Williamson, M.D. |
Participants | Members, NCORP, Medical Oncologists |
Closure Date | 2003-02-01 |
Amendments, Revisions, Memoranda
SWOG Revision #2 regarding GOG Revision #7
A Phase III Randomized Trial of Paclitaxel and Carboplatin Versus Triplet or Sequential Doublet Combinations in Patients with Epithelial Ovarian or Primary Peritoneal Carcinoma.
Study Coordinator(s) | Amy D. Tiersten, M.D. |
Participants | NCORP, Members, Surgeons, Pathologists |
Amendment #2 regarding NCCTG Addendum #7
Phase III Trial of Doxorubicin and Cyclophosphamide (AC) Followed by Weekly Paclitaxel With or Without Trastuzumab as Adjuvant Treatment for Women With HER-2 Overexpressing or Amplified Node Positive or High-Risk Node Negative Breast Cancer
Study Coordinator(s) | Silvana Martino, D.O. |
Participants | Members, NCORP, Affiliates, Medical Oncologists, Surgeons |
Revision # 4
A Phase II Trial of Epothilone B Analogue BMS-247550 (NSC #710428) Every 21 Days in Patients With Advanced Pancreas Cancer
Study Coordinator(s) | Robert P. Whitehead, M.D. |
Participants | Members, NCORP |
Amendment #2
A Phase III Trial of Dexamethasone, Cyclophosphamide, Etoposide, Cisplatin (DCEP) and G-CSF With or Without Thalidomide (NSC #66847) as Salvage Therapy for Patients with Refractory Multiple Myeloma
Study Coordinator(s) | Mohamad A. Hussein, M.D., James K. Weick, M.D. |
Participants | NCORP, Members |
Other New Items
- IP - Pts Must Be Informed
- AC - Consent Must Be Amended
- CBR - No Registration Allowed until IRB Review
- RC - Formal Re-consent Required
- FBR - Full Board Review Required
- ER - Expedited Review Acceptable
- NR - No IRB Review Required