drugset / Trial / NCT01226316

Safety, Tolerability & Potential Anti-cancer Activity of Increasing Doses of AZD5363 in Different Treatment Schedules

NCT01226316

Phase 1 Completed 285 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is designed to investigate the safety and tolerability of a new drug, AZD5363, in patients with advanced cancer - and to identify a dose and schedule that can be used in the future. This study will also investigate how the body handles AZD5363 (ie, how quickly the body absorbs and removes the drug). This study will also investigate anti-tumour activity of AZD5363 in patients with advanced / metastatic breast, gynaecological cancers or other solid cancers bearing either AKT1 / PIK3CA or PTEN mutation.

Timeline

Start
2010-12-01
Primary completion
2019-04-26
Completion
2024-12-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Capivasertib Small molecule 320 mg Oral
Subject Capivasertib Small molecule 400 mg Oral
Subject Capivasertib Small molecule 480 mg Oral
Subject Capivasertib Small molecule 640 mg Oral