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Risk-adapted, Proteomic-guided Systemic Therapy for Previously Untreated Advanced Non-small Cell Lung Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a phase 2, pragmatic, 1:1 randomized, open-label study that evaluates risk-adapted, proteomic-guided systemic therapy to improve 12-month progression free survival (PFS) among patients with previously untreated advanced non-small cell lung cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants must have histologically confirmed non-small cell lung cancer that is metastatic or unresectable (stage IIIC or IV), deemed appropriate to receive standard of care immune checkpoint inhibitor-based therapy given with palliative intent.

• Age ≥18 years at the time of consent.

• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥50%).

• Ability to understand and willingness to sign the informed consent form (ICF).

• Stated ability and willingness to adhere to all protocol requirements while on study

Locations
United States
California
University of California Davis Comprehensive Cancer Center
RECRUITING
Sacramento
Contact Information
Primary
Surbhi Singhal, MD
susinghal@health.ucdavis.edu
(916) 734-3772
Time Frame
Start Date: 2026-01-30
Estimated Completion Date: 2036-12
Participants
Target number of participants: 56
Treatments
Experimental: Systemic immune checkpoint inhibitor (ICI)-based therapy informed by PROphet CB and CARG-TT
Active_comparator: Standard of Care
Standard of care (SOC) biomarker assessment and subsequent selection of SOC systemic therapy.
Sponsors
Collaborators: National Cancer Institute (NCI)
Leads: University of California, Davis

This content was sourced from clinicaltrials.gov

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