Risk-adapted, Proteomic-guided Systemic Therapy for Previously Untreated Advanced Non-small Cell Lung Cancer
Recruiting
Phase 2Interventional Study
Non-small Cell Lung Cancer Stage IIICNon-small Cell Lung Cancer Stage IVNon Small Cell Lung CancerNon-small Cell Lung Cancer MetastaticNon-small Cell Lung Cancer Unresectable
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
56 (estimated)
Sponsor
University of California, Davis · Other
Who this trial is looking for
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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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 …
Inclusion Criteria:
* 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
Exclusion Criteria:
* Tumor with known sensitizing alteration in ALK, EGFR, HER2, MET exon 14, NTRK, RET, or ROS1.
* Medical comorbidities precluding immune checkpoint inhibitor-based therapy per treating investgator's discretion.
* Previous systemic therapy for metastatic Stage IIIC or IV NSCLC. Patients who previously completed systemic therapy for early stage or locally advanced NSCLC ≥ 80 days prior to trial registration are eligible for inclusion.
* Any condition that in the opinion of the investigator would interfere with the participant's safety or compliance while on study
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