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Imaging Perfusion Restrictions From Extracellular Solid Stress - An Open-label Losartan Study — ImPRESS  

Glioblastoma Clinical Trial

Official title:
Imaging Perfusion Restrictions From Extracellular Solid Stress - An Open-label Losartan Study

Clinical Trial Summary

An open-label, single institutional phase II trial of losartan in patients with primary and metastatic brain tumors with an individual stepped-wedge, randomized, assessor-blinded, dose-finding design on three indications.

Clinical Trial Description

For this study losartan, an angiotensin-II inhibitor, is defined as the Investigational Medicinal Product (IMP). The focus of the study is to assess the dose-response relationship of losartan on imaging-based measures of tissue perfusion and mechanical forces in patients with brain tumors. We hypothesize that losartan improves the effect of traditional cancer treatment by alleviating mechanical forces (solid stress) of the tumor microenvironment to improve tissue perfusion, while administration of losartan alone has little effect on cancer patients. This is an open-label study and no active comparator or placebo will be used. Study participants include adult patients with newly diagnosed- and recurrent glioblastoma, as well as adult patients with metastatic brain tumors from non-small cell lung cancer. The study will assess the safety of losartan treatment and its dose-response relationship on conventional and experimental radiographic characteristics when used alone or as an add-on to standard cancer treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03951142
Study type Interventional
Source Oslo University Hospital
Contact
Status Enrolling by invitation
Phase Phase 2
Start date October 1, 2019
Completion date December 31, 2024
View Details
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