drugset / Trial / NCT04341181

ProTarget - A Danish Nationwide Clinical Trial on Targeted Cancer Treatment Based on Genomic Profiling

NCT04341181

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The ProTarget study is a phase II, prospective, non-randomized clinical trial with the primary purpose of investigating the safety and efficacy of commercially available cancer drugs that target specific changes in cancer cell DNA to treat patients with advanced cancer. The primary endpoint is anti-tumor activity or stable disease documented after 16 weeks of experimental drug treatment. The drugs used in the trial have been approved by EMA/FDA for the treatment of certain cancers. Choice of drug is based on whether the patient's cancer cells contain precisely the DNA change (i) targeted by the EMA/FDA-approved drug or (ii) related to sensitivity to the EMA/FDA-approved drug. The trial drug is thus not approved by the EMA/FDA or in Denmark for the treatment of the patient's cancer - it is so-called "off-label use". The secondary purposes are: * To detect side effects in patients treated with commercially available targeted cancer drugs. * Performing biomarker analyzes, including (but not limited to) whole-genome analysis (WGS) on a fresh tumor tissue sample (biopsy) at baseline and progression. * To investigate mechanisms of resistance using recurrent / serial fresh tumor biopsies for WGS and so-called liquid biopsies, which are blood samples in which the cancer cell DNA is analyzed. The secondary endpoints include response duration, progression-free survival, and overall survival.

Timeline

Start
2020-08-24
Primary completion
2029-04-30
Completion
2030-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Alectinib Small molecule
Subject Atezolizumab Monoclonal antibody
Subject Avelumab Monoclonal antibody
Subject Axitinib Small molecule
Subject Cobimetinib Small molecule
Subject Erlotinib Small molecule
Subject Niraparib Small molecule
Subject Pertuzumab Monoclonal antibody
Subject Trastuzumab Monoclonal antibody
Subject Trastuzumab emtansine Other / unclassified
Subject Vemurafenib Small molecule
Subject Vismodegib Small molecule

Indications