drugset / Trial / NCT02617277

Safety, Tolerability and Pharmacokinetics of AZD1775 (Adavosertib) Plus MEDI4736 (Durvalumab) in Patients With Advanced Solid Tumours

NCT02617277

Phase 1 Completed 56 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will assess the safety, tolerability, and pharmacokinetics of AZD1775 (adavosertib) given orally in combination with intravenous MEDI4736 (durvalumab). Secondly, the immunogenicity, pharmacodynamics, and preliminary anti-tumour activity will be determined in patients with refractory solid tumours.

Timeline

Start
2015-12-28
Primary completion
2019-04-22
Completion
2026-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Adavosertib Small molecule 125 mg Oral
Subject Adavosertib Small molecule 150 mg Oral
Subject Adavosertib Small molecule 300 mg Oral
Subject Durvalumab Monoclonal antibody 1500 mg Intravenous

Indications