 |
| A Phase I, Open-Label, Dose Escalation Study of Daily Dosing with BB-10901. |
| Pancreatica Trial ID: PA-7558 |
 |
| Trial Phase |
 |
Alternative Drug Names |
 |
| Phase 1 |
 |
|
 |
 |
| Disease Stage (least advanced) |
 |
Tumor Type |
 |
| Advanced |
 |
Neuroendocrine tumor (e.g. islet-cell tumor) |
 |
 |
| Treatment |
 |
| Immunotherapy (includes vaccines) |
 |
|
 |
| Drug and Trial Classifications and Mechanisms |
 |
| monoclonal antibody |
 |
|
 |
| Special Inclusion Criteria |
 |
| -Not Specified- |
 |
 |
| Main Exclusion Criteria |
 |
| Liver / kidney function requirements? Yes |
| Activity status requirements? Yes |
 |
 |
| Prior Therapy Allowed? |
 |
| Chemo or Biological? Selectively Allowed |
| Radiation? Selectively Allowed |
| Surgery? Selectively Allowed |
| Other? Not Specified |
 |
 |
| Treatment Interval |
 |
| 16 to 31 days |
 |
 |
| Institutions |
 |
| Baystate Regional Cancer Program |
| Springfield, MA, US |
 |
| Ohio State University |
| Columbus, OH, US |
 |
| M.D. Anderson Cancer Center, University of Texas |
| Houston, TX, US |
 |
| Christie Hospital N.H.S. Trust |
| Manchester , England |
 |
| Cancer Research Centre at Weston Park Hospital |
| Sheffield, England |
 |
| Royal Marsden Hospital |
| Sutton, Surrey, England |
 |
|
|
|