CompletedPhase 1NCT03326752

Phase 1b DV281 With an Anti-PD-1 Inhibitor in NSCLC

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).

Checked against the public recordLast updated Jun 17, 2020 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 1
U.S. locations6
SponsorDynavax Technologies Corporation
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Dynavax Technologies Corporation
Interventions being studied
Drug: DV281; Device: Breath Actuated Nebulizer; Drug: DV281 (RP2D); Drug: Approved Anti-PD-1 Inhibitor
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

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

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Moores UC San Diego Cancer CenterLa Jolla, California
  • Ronald Reagan University of California Los Angeles Medical CenterSanta Monica, California
  • Allina Health, Virginia Piper Cancer InstituteMinneapolis, Minnesota
  • Sarah Cannon Research InstituteNashville, Tennessee
  • Virginia Cancer SpecialistsFairfax, Virginia
  • Seattle Cancer Care AllianceSeattle, Washington

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jun 17, 2020. Always confirm current availability with the study team.

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