Cancer Patient Remote Monitoring for Timely Communication Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAsklepios proresearch

About this trial

The study is designed as a prospective, single-arm observational, mixed-method study. Patients with stage IV NSCLC or inoperable mesothelioma will be included and will be treated with immunotherapy according to current guidelines and standard of care. Patients may receive either a PD1/L1 inhibitor monotherapy or, if indicated, together with a CTLA4 inhibitor. Immunotherapy may be administered alone or together with chemotherapy as per site standard/physician's choice. Patients will be given access to a mobile app. Patients will receive daily questions via the app to assess immune-related adverse events between clinic visits and their well-being.

Eligibility criteria

Qualifiers

Signed Informed Consent Form

Age > 18 years at the time of study entry

Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2

Life expectancy > 6 months

Disqualifiers

Previous systemic treatment for metastatic or locally advanced disease

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 2 trial groups

Locations

This trial has no locations

Sponsors and collaborators

Asklepios proresearch

Lead sponsor

Q1.6 B.V.

Collaborator

Medical University of Vienna

Collaborator