drugset / Trial / NCT00349934
IMP321 Plus First-line Paclitaxel in Metastatic Breast Carcinoma
Non-randomizedParallel-groupOpen-labelTreatment
Summary
Open label, non-randomized, fixed dose-escalation phase I study, performed in ambulatory setting in patients receiving as a first line chemotherapy for metastatic breast carcinoma the standard 6 cycles of weekly paclitaxel (80 mg/m² at D1, D8 and D15 of a 4-week cycle). Three IMP321 doses (0.25, 1.25 and 6.25 mg) will be tested and given at D2 and D16 of this 4-week cycle, for 6 courses.
Timeline
- Start
- 2006-07
- Primary completion
- 2009-11
- Completion
- 2010-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IMP321 | Protein / enzyme biologic | 0.25 mg | Subcutaneous |
| Subject | IMP321 | Protein / enzyme biologic | 1.25 mg | Subcutaneous |
| Subject | IMP321 | Protein / enzyme biologic | 6.25 mg | Subcutaneous |