drugset / Trial / NCT03411161

S 81694 Plus Paclitaxel in Metastatic Breast Cancer

NCT03411161 ↗

Phase 1/2 Completed 22 enrolled Servier ADIR, a Servier Group company · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety profile, the maximum tolerated dose (MTD) and the associated dose-limiting toxicities (DLTs) of S 81694 in combination with paclitaxel in metastatic breast cancer (mBC) patients, and to investigate the antitumour activity of the combination in metastatic triple negative breast cancer (mTNBC) patients.

Timeline

Start
2018-01-04
Primary completion
2020-06-08
Completion
2020-06-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Paclitaxel Small molecule 80 mg/m2 Intravenous
Subject S 81694 Unknown — Intravenous