A Phase I/II Study of MEDI4736 in Combination With Olaparib in Patients With Advanced Solid Tumors.

第1/2相 実施中（募集終了） NCT02734004

概要

The purpose of this study is to look at the effectiveness, safety, and antitumor activity of study drugs MEDI4736 in combination with olaparib (modules 1, 2, 3, 4, 5 and 7) and MEDI4736 in combination with olaparib and bevacizumab (module 6). It will also examine what happens to the study drugs in the body and investigate how well the combination between MEDI4736, olaparib and bevacizumab is tolerated.

Initial Stage Cohorts: Disease Control Rate (DCR) at Week 12

RECIST performed at baseline, at 4 weeks after first dose of olaparib monotherapy and every 8 weeks +/-7 days thereafter. Assessed until DCO 14 Jun 2019. · percentage of participants

Second Stage Cohort: Objective Response Rate (ORR)

RECIST performed at baseline, and every 8 weeks +/-7 days thereafter. Assessed until 17 Sep 2021. · percentage of participants

Second Stage Cohorts: DCR at Week 24

RECIST performed at baseline, and every 8 weeks +/-7 days thereafter. Assessed until 17 Sep 2021. · percentage of participants

BENITIONS で見る ClinicalTrials.gov の原文を見る

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すべての治験