This open-label, multicenter, dose-escalation and expansion trial is designed to evaluate the safety and preliminary efficacy of inhaled DV281 in combination with nivolumabfor the treatment of NSCLC and to select a recommended phase 2 dose (RP2D).
Pre-clinical studies support the proposed dosing schema to be tested and a potential benefit of the combination of inhaled DV281 with nivolumab for subjects with advanced NSCLC. This study (DV9-NSC-01) is designed for establishing an immunologically optimal RP2D for inhaled DV281 in combination with an approved anti-PD-1 inhibitor. This trial, studying the potential to enhance the efficacy of an approved anti-PD-1 inhibitor in subjects with advanced NSCLC, addresses an unmet need for NSCLC patients having tumors that do not respond or do not respond adequately to anti-PD-1 inhibitor monotherapy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
\- Dose Escalation will be the preliminary dose finding phase of the study. Subjects will be enrolled to available Dosing Cohorts.
Breath-actuated, electronic system designed to aerosolize liquid medication.
\- Dose Expansion will be enrolled into 4 groups based on NSCLC characteristics.
Moores UC San Diego Cancer Center
La Jolla, California, United States
Ronald Reagan University of California Los Angeles Medical Center
Santa Monica, California, United States
Allina Health, Virginia Piper Cancer Institute
Minneapolis, Minnesota, United States
Sarah Cannon Research Institute
Nashville, Tennessee, United States
Dose Escalation
Incidence of dose-limiting toxicities (DLTs)
Time frame: DLT assessment period - Day 1 through Day 28.
Dose Expansion
Objective response rate (ORR) of dosing regimen established during the Dose Escalation
Time frame: 1 year after last subject is enrolled in the Dose Expansion phase of study
Dose Expansion
Duration of Response (DOR) and time to response.
Time frame: 1 year after last subject is enrolled in the Dose Expansion phase of the Study
Dose Escalation
Assess IFN-a induced gene expression in blood when DV281 is administered as a monotherapy and in combination with an approved anti-PD-1 inhibitor
Time frame: IFN response assessment period - Day 1 through Day 21
Dose Expansion
Incidence of treatment related AE's as assessed by CTCAE Version 4.03
Time frame: 1 year after last subject is enrolled in the Dose Expansion phase of study
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
FDA approved Anti-PD-1 Inhibitor
Virginia Cancer Specialists
Fairfax, Virginia, United States
Seattle Cancer Care Alliance
Seattle, Washington, United States