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AstraZeneca D4194C00008

Trial Overview

Official Title

Prospective, Interventional Pilot Study Of Mobile Devices And Digital Applications To Detect Early Pneumonitis And Other Pulmonary Adverse Events In Unresectable Stage Iii Non-Small Cell Lung Cancer Patients On Durvalumab

Study Purpose

To test new technology that monitors your respiratory function data, oxygen saturation levels, vital signs, and physical movement data without affecting your daily life in a significant way.

Diagnosis

Patients have unresectable Stage III non-small cell lung cancer and your doctor has prescribed durvalumab as treatment.

Eligibility

Unresectable Stage III NSCLC

No progression post platinum based chemo/radiation

Must be eligible for durvalumab

Cannot be O2 dependence.

Patients must sign an approved informed consent and authorization permitting release of personal health information.

Intervention

Patients will wear a mobile device to collect V/S to help detect early symptoms of pneumonitis during Durvalumab treatment.

Patients will have an introductory Baseline visit, several routine visits needed for your standard cancer treatment, an End-of-Study visit after about 12 months and a follow-up visit 30 days after the End-of-Study visit.

You will use the devices and tablet application to record data at home every day.

For more information, visit ClinicalTrials.gov

Key Participation Requirements
Gender
Male or Female
Age
19 years and older
Phase
Phase III
Methodist Health System Trial Code
AstraZeneca D4194C00008