drugset / Trial / NCT02338349

A Phase I, Multicenter, Open-Label, Multi-Part, Dose-escalation Study of RAD1901 in Postmenopausal Women With Advanced Estrogen Receptor Positive and HER2-Negative Breast Cancer

NCT02338349

Phase 1 Completed 57 enrolled Stemline Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and preliminary efficacy of elacestrant (RAD1901) in patients with advanced ER+, HER2-negative breast cancer.

Timeline

Start
2015-01
Primary completion
2019-09
Completion
2020-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Elacestrant Other / unclassified 400 mg Oral