drugset / Trial / NCT00349934

IMP321 Plus First-line Paclitaxel in Metastatic Breast Carcinoma

NCT00349934

Phase 1 Completed 33 enrolled Immutep S.A.S. Umanis · collab
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

EvaluationDrugModalityDoseRoute
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

Indications