Phase 1b DV281 With an Anti-PD-1 Inhibitor in NSCLC
Advanced Non Small Cell Lung Cancer

About this trial
This is an interventional treatment trial for Advanced Non Small Cell Lung Cancer focused on measuring Cancer, Lung Cancer, NSCLC, Anti-PD-1 inhibitor, Immuno-oncology, Toll-Like Receptor (TLR) agonist
Eligibility Criteria
Inclusion Criteria:
- Have documented histologically or cytologically confirmed advanced NSCLC as the dominant histology.
- If confirmed EGFR or ALK directed testing warrants actionable targeted therapy, must have confirmed disease progression on targeted therapy or cannot tolerate targeted therapy.
- Aged 18 years and older on the day of signing informed consent
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 to 2 for Dose Escalation phase and ECOG PS 0 to 1 for Dose Expansion phase
- Adequate organ function as indicated by laboratory values
- Life expectancy, in the opinion of the investigator, of at least 3 months
Exclusion Criteria
- Condition of the subjects lung anatomy is such that proper delivery of inhaled DV281 to the specific location of intra-thoracic tumor(s) could be compromised
- Any known additional malignancy that is progressing or required active treatment in the last 3 years
- Current or history of clinically significant non-infectious pneumonitis
- History of clinically severe lung disease, asthma, or chronic obstructive pulmonary disease (COPD) requiring emergency management and/or hospitalization in the last year
- Received more than 30 Gy of conventional radiation therapy in the thoracic region within 26 weeks prior to study enrollment
- Is expected to require any other form of anti-cancer therapy while in the trial. Zoledronic acid or denosumab as supportive care for bone metastases will be allowed if started prior to study enrollment
- Diagnosis of immunodeficiency or is receiving systemic steroid therapy (>10 mg of prednisone or equivalent) or any other form of immunosuppressive therapy (including immune modulators or systemic corticosteroids) that cannot be discontinued safely within 14 days prior to study enrollment
- Has a medical condition that requires immunosuppression
- Active autoimmune disease requiring systemic treatment in the past 2 years or a disease that requires immunosuppressive medication including systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, Sjogren's syndrome, or autoimmune thrombocytopenia. Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment.
- Known central nervous system metastases, brain metastases, or carcinomatous meningitis
Sites / Locations
- Moores UC San Diego Cancer Center
- Ronald Reagan University of California Los Angeles Medical Center
- Allina Health, Virginia Piper Cancer Institute
- Sarah Cannon Research Institute
- Virginia Cancer Specialists
- Seattle Cancer Care Alliance
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Dose Escalation Cohort 1-5
Dose Expansion (RP2D)
Cohort 1-4 DV281 - Dose Level 1-5 DV281 in combination with nivolumab DV281 is administered via a breath actuated nebulizer
4 Cohorts Preliminary Recommended Phase 2 dosing of DV281 in combination with nivolumab Cohort 1: Non-squamous and non-EGFR/ ALK mutation and progressed on anti-PD-1/L1 therapy Cohort 2: Non-squamous and EGFR/ ALK mutation and progressed on targeted therapy Cohort 3: Squamous and anti-PD-1/ L1 therapy experienced Cohort 4: Squamous and anti-PD-1/L1 therapy naive DV281 is administered via a breath actuated nebulizer.