drugset / Trial / NCT03284957

Phase 1/2 Study of Amcenestrant (SAR439859) Single Agent and in Combination With Other Anti-cancer Therapies in Postmenopausal Women With Estrogen Receptor Positive Advanced Breast Cancer

NCT03284957

Phase 1/2 Terminated 136 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary Objectives: Dose Escalation: * To assess the incidence rate of dose-limiting toxicity (DLT) and to determine the maximum tolerated dose (MTD) as well as the recommended dose (RD) of amcenestrant administered as monotherapy and in combination with palbociclib * To assess the incidence rate of DLT and determine the RD of everolimus or abemaciclib in combination with the selected amcenestrant dose for the combination therapy Safety Run-In: \- To confirm the RD of amcenestrant in combination with alpelisib Dose Expansion: * Antitumor activity using objective response rate (ORR) * Overall safety profile of amcenestrant administered in combination with palbociclib, alpelisib, everolimus, and abemaciclib Secondary Objectives: * Overall safety profile of amcenestrant monotherapy and in combination * Pharmacokinetic (PK) profile of amcenestrant administered as monotherapy or in combination and PK profile of palbociclib, alpelisib, everolimus and abemaciclib * Antitumor activity using ORR, the clinical benefit rate (CBR) and progression free survival (PFS) * Time to first tumor response * Residual ER availability with positron emission tomography (PET) scan \[(18)F\] fluoroestradiol (18F-FES) uptake with increasing doses of amcenestrant * Food effect on PK of amcenestrant * Potential induction/inhibition effect of amcenestrant on cytochrome P450 (CYP) 3A using 4b-OH cholesterol

Timeline

Start
2017-09-20
Primary completion
2024-11-08
Completion
2024-11-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Abemaciclib Small molecule
Subject Alpelisib Small molecule Oral
Subject Amcenestrant Other / unclassified 20 mg Oral
Subject Amcenestrant Other / unclassified 400 mg Oral
Subject Amcenestrant Other / unclassified 600 mg Oral
Subject Everolimus Small molecule
Subject Palbociclib Small molecule Oral

Indications