Trial Search Results

Study to Compare the Safety and Efficacy of CMB305 With Atezolizumab to Atezolizumab Alone in Participants With Sarcoma (IMDZ-C232/V943A-002)

This is an open-label Phase 2 randomized study that will examine the use of the study agents, CMB305 (sequentially administered LV305 which is a dendritic cell-targeting viral vector expressing the New York Esophageal Squamous Cell Carcinoma 1 gene [NY-ESO-1] and G305 which is a NY-ESO-1 recombinant protein plus glucopyranosyl lipid adjuvant-stable emulsion [GLA-SE]) in combination with atezolizumab or atezolizumab alone, in participants with locally advanced, relapsed or metastatic sarcoma (synovial or myxoid/round cell liposarcoma) expressing the NY-ESO-1 protein.

There is no formal primary hypothesis for this study.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Immune Design

Collaborator: Genentech, Inc.

Stanford Investigator(s):

Intervention(s):

  • Biological: CMB305
  • Biological: atezolizumab

Phase:

Phase 2

Eligibility


Inclusion Criteria:

   - Locally advanced, relapsed, or metastatic sarcoma with measurable tumor burden
   following therapy, as defined by Response Evaluation Criteria in Solid Tumors Version
   1.1 (RECIST 1.1); the total of all lesions must be ≤12 cm (for synovial sarcoma) or
   ≤15 cm (for myxoid/round cell liposarcoma [MRCL])

   - Tumor histology consistent with synovial sarcoma or MRCL

   - Tumor specimen positive for NY-ESO-1 expression by immunohistochemistry (IHC)

   - Inadequate response, relapse, and/or unacceptable toxicity with ≥1 prior systemic,
   surgical, or radiation cancer therapies

   - Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Exclusion Criteria:

   - Investigational therapy within 4 weeks prior to CMB305 dosing

   - Prior administration of other NY-ESO-1-targeting immunotherapeutics

   - Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including
   anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), anti-programmed cell death
   receptor 1 (PD-1), and anti-programmed cell death ligand (PD-L1) therapeutic
   antibodies, or any other antibody or drug targeting T-cell costimulation

   - Treatment with systemic immunostimulatory agents (including but not limited to
   interleukin-2) within 4 weeks or five half-lives of the drug, whichever is shorter,
   prior to first dose

   - Significant immunosuppression

   - Other cancer therapies, including chemotherapy, radiation, biologics or kinase
   inhibitors within 3 weeks prior to the first scheduled dosing

   - History of autoimmune disease, including but not limited to myasthenia gravis,
   myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis,
   inflammatory bowel disease, vascular thrombosis associated with antiphospholipid
   syndrome, Wegener's granulomatosis, Sjögren's syndrome, Guillain-Barré syndrome,
   multiple sclerosis, vasculitis, or glomerulonephritis

   - History of idiopathic pulmonary fibrosis (including pneumonitis), drug-induced
   pneumonitis, organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic
   organizing pneumonia), risk of pulmonary toxicity, or evidence of active pneumonitis
   on screening chest computed tomography (CT) scan. History of radiation pneumonitis in
   the radiation field (fibrosis) is permitted

   - History of other cancer within 3 years

   - Evidence of active tuberculosis or recent (<1 week prior to first scheduled dosing)
   clinically significant infection requiring systemic therapy

   - Evidence of active hepatitis B (HepB), hepatitis C (HepC), or Human Immunodeficiency
   Virus (HIV) infection

   - Known active or untreated central nervous system (CNS) metastases

   - Pregnant, planning to become pregnant within 6 months of treatment, or nursing

   - Known allergy(ies) to any component of CMB305, atezolizumab, or severe allergic
   reactions to monoclonal antibodies, fusion proteins, or Chinese hamster ovary (CHO)
   cell products

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting