drugset / Trial / NCT04644432

Individualized Treatment Strategy for Patients With Metastatic Non-clear Cell Renal Cell Carcinoma

NCT04644432

Phase 2 Unknown 30 enrolled Herlev and Gentofte Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the open-label INDIGO-study is to examine whether a first line individualized treatment strategy based on DNA and RNA analyses from the patient's tumor is feasible. Moreover, to involve the patient further in their treatment via patient-reported outcomes (PRO) measurements in a value-based healthcare setup with simultaneous analyses of the financial costs of this strategy. The patients are assigned into 4 treatment arms according to the results of their DNA and RNA analyses. All patients receive electronic questionnaires regarding symptoms and side effects weekly and questionnaires regarding quality of life monthly. Based on each patient's answers of the questionnaires the patient receives advices in the app to reduce the symptoms and side effects or the patient is instructed to contact the hospital. The hypothesis: Basing the choice of first-line treatment for DNA mutations and RNA profiles in a heterogeneous patient population increases the overall response rate for the total population to 30% compared to 10% for historical cohorts.

Timeline

Start
2020-03-06
Primary completion
2022-09-06
Completion
2022-09-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Alectinib Small molecule 600 mg
Subject Cabozantinib Small molecule 60 mg
Subject Crizotinib Small molecule 250 mg
Subject Dabrafenib Small molecule 150 mg
Subject Erlotinib Small molecule 150 mg
Subject Imatinib Small molecule 400 mg
Subject Nivolumab Monoclonal antibody 6 mg/kg Intravenous
Subject Olaparib Small molecule 400 mg
Subject Osimertinib Small molecule 80 mg
Subject Palbociclib Small molecule 125 mg
Subject Pembrolizumab Monoclonal antibody 2 mg/kg Intravenous
Subject Sunitinib Small molecule 50 mg Oral
Subject Trametinib Small molecule 2 mg
Subject Trastuzumab-emtansin Unknown 3.6 mg/kg Intravenous

Indications