drugset / Trial / NCT01367002

Evaluation of Carboplatin/Paclitaxel With and Without Trastuzumab (Herceptin) in Uterine Serous Cancer

NCT01367002 ↗

Phase 2 Completed 61 enrolled Yale University Genentech, Inc. · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to estimate whether the addition of trastuzumab to paclitaxel and carboplatin chemotherapy improves progression free survival when compared to paclitaxel and carboplatin alone in Uterine Serous Papillary Carcinoma (USPC) patients overexpressing Her2/neu at 3+ level by immunohistochemistry (IHC)or positive by fluorescence in situ hybridization (FISH).

Timeline

Start
2011-06
Primary completion
2022-06-30
Completion
2022-06-30

Outcome

Met primary endpoint

paper median progression-free survival was 8.0 months (control) versus 12.6 months (experimental; P = .005; hazard ratio [HR], 0.44; 90% CI, 0.26 to 0.76). PMID 29584549 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Trastuzumab Monoclonal antibody 6 mg/kg Intravenous
Comparator Carboplatin Small molecule 5 unknown Intravenous
Comparator Paclitaxel Small molecule 175 mg/m2 Intravenous

Indications