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NOT YET RECRUITING
NCT06623786

Cancer Patient Remote Monitoring for Timely Communication Study

Sponsor: Asklepios proresearch

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2024-10

Completion Date

2026-04

Last Updated

2024-10-02

Healthy Volunteers

No

Conditions