drugset / Trial / NCT01980277

Phase Ib/II Study of LY2780301 in Combination With Weekly PACLITAXEL in HER2-metastatic Breast Cancer

NCT01980277 ↗

Phase 1/2 Terminated 68 enrolled Institut Paoli-Calmettes
NaSingle-groupOpen-labelTreatment

Summary

The overall rationale of this study evaluating tolerance and efficacy of LY2780301 in combination with paclitaxel in HER2-negative, inoperable locally advanced or metastatic breast cancer (MBC) is based on : * the medical need in this population with either hormonal-resistant or unsensitive and/or rapidly progressive disease * the preclinical evidences for involvement of PI3K/AKT pathway in tumor progression and drug resistance, including taxanes as well as its potential reversion by AKT inhibition * the high level of frequency of PI3K/AKT activation in HER2-negative MBC * the in vitro and in vivo preclinical activity of LY2780301, and its synergistic combination with various anticancer agents, including taxanes * the favourable profile of tolerance of LY2780301 in phase I trial Weekly paclitaxel is conventionally administered at 80 mg/m²/week and is a standard treatment in breast cancer (BC) As described above, LY2780301 500 mg once daily has been established as the RP2D in phase I single agent trial. Evidence of pharmacodynamic activity was noted at 400-500 mg QD. Conservatively, the first dose level to be explored will be LY2780301 400 mg QD and paclitaxel 70 mg/m²/week.

Timeline

Start
2014-01
Primary completion
2017-05
Completion
2018-12-12

Outcome

Outcome not reported

Stopped: “Drug development stopped”

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2780301 Unknown 300 mg Oral
Subject LY2780301 Unknown 400 mg Oral
Subject LY2780301 Unknown 500 mg Oral
Subject Paclitaxel Small molecule 70 mg/m2 Intravenous
Subject Paclitaxel Small molecule 80 mg/m2 Intravenous

Indications