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Clinical Trial Record

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Atezolizumab Combined With BDB001 AnD Immunogenic Radiotherapy in Patients With Advanced Solid Tumors

2021-03-31

2024-09

2026-03

247

Study Overview

Atezolizumab Combined With BDB001 AnD Immunogenic Radiotherapy in Patients With Advanced Solid Tumors

Basket trial concept to independently and simultaneously assess the effects of the association of atezolizumab + BDB001 + radiotherapy in multiple solid tumors.

6 independent, multicenter, prospective, single-arm phase II trials, based on 2-stage Simon's optimal design, will be conducted in parallel to assess the efficacy of atezolimab + BDB001+ radiotherapy, separately, in distinct populations of solid tumors: * Population 1: pancreatic cancer * Population 2: virus-associated tumors * Population 3: anti-PD-1/L1 refractory non-small lung cancer * Population 4: soft-tissue sarcoma * Population 5: anti-PD-1/L1 refractory bladder cancer * Population 6: triple negative breast cancer

  • Solid Tumor, Adult
  • Pancreatic Cancer
  • Virus-associated Tumors
  • Non Small Cell Lung Cancer
  • Melanoma
  • Bladder Cancer
  • Triple Negative Breast Cancer
  • DRUG: Association atezolizumab + BDB001 + RT
  • DRUG: Association atezolizumab + BDB001+ RT
  • DRUG: Association atezolizumab + BDB001+ RT
  • DRUG: Association atezolizumab + BDB001 + RT
  • DRUG: Association atezolizumab + BDB001 + RT
  • DRUG: Association atezolizumab + BDB001 + RT
  • IB 2019-01
  • 2019-000850-78 (EUDRACT_NUMBER Identifier) (EUDRACT_NUMBER: )

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2019-04-08  

N/A  

2024-05-21  

2019-04-10  

N/A  

2024-05-22  

2019-04-16  

N/A  

2024-05  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment

Allocation:
Non Randomized

Interventional Model:
Parallel

Masking:
None

Arms and Interventions

Participant Group/ArmIntervention/Treatment
EXPERIMENTAL: Population 1: Pancreatic cancer

Participants with pancreatic cancer will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001 + RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
EXPERIMENTAL: Population 2: Virus-associated tumors

Participants with virus-associated tumors will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001+ RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
EXPERIMENTAL: Population 3: anti-PD-1/L1 refractory non-small lung cancer

Participants with anti-PD-1/L1 refractory non-small lung cancer will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001+ RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
EXPERIMENTAL: Population 4: Soft-tissue sarcoma

Participants with soft-tissue sarcoma will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001 + RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
EXPERIMENTAL: Population 5: anti-PD-1/L1 refractory bladder cancer

Participants with anti-PD-1/L1 refractory bladder cancer will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001 + RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
EXPERIMENTAL: Population 6: Triple negative breast cancer

Participants with triple negative breast cancer will be treated with Atezolizumab combined with BDB001 and radiotherapy.

DRUG: Association atezolizumab + BDB001 + RT

  • A treatment cycle consits of 3 weeks. Atezolizumab will be administered as a 1-hour infusion on day 1 every 3 weeks (1200 mg). BDB001 will be administered by a 30-minute intravenous infusion before atezolizumab, on Days 1, 8, and 15 of cycles 1, 2, and 3
Primary Outcome MeasuresMeasure DescriptionTime Frame
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with pancreatic cancer.Antitumor activity will be assessed in terms of disease control rate within 24 weeks of treatment onset and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed within 24 weeks of treatment onset (while treated with the investigational product), based on RECIST 1.1 criteria.Within 6 months of treatment onset
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with virus associated tumors.Antitumor activity will be assessed in terms of disease control rate within 24 weeks of treatment onset and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed within 24 weeks of treatment onset (while treated with the investigational product), based on RECIST 1.1 criteria.Within 6 months of treatment onset
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with non-small cell lung cancer.Antitumor activity will be assessed in terms of disease control rate within 24 weeks of treatment onset and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed within 24 weeks of treatment onset (while treated with the investigational product), based on RECIST 1.1 criteria.Within 6 months of treatment onset
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with soft-tissue sarcoma.Antitumor activity will be assessed in terms of 6-month progression-free rat (PFR) and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed at 6 months following treatment onset and more than 24 weeks, based on RECIST 1.1 criteria.6 months of treatment onset
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with bladder cancer.Antitumor activity will be assessed in terms of disease control rate within 24 weeks of treatment onset and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed within 24 weeks of treatment onset (while treated with the investigational product), based on RECIST 1.1 criteria.Within 6 months of treatment onset
Assessment of the antitumor activity of atezolizumab combined with BDB001 and radiotherapy in patients with triple negative breast cancer.Antitumor activity will be assessed in terms of disease control rate within 24 weeks of treatment onset and is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease (SD) observed within 24 weeks of treatment onset (while treated with the investigational product), based on RECIST 1.1 criteria.Within 6 months of treatment onset
Secondary Outcome MeasuresMeasure DescriptionTime Frame
6-month Progression-free rate (PFR) in patients with pancreatic cancer.Progression-free rate is defined as the rate of complete or partial response (CR, PR) or stable disease (SD), as per RECIST 1.1 criteria.6 months
6-month Progression-free rate (PFR) in patients with virus-associated tumor.Progression-free rate is defined as the rate of complete or partial response (CR, PR) or stable disease (SD), as per RECIST 1.1 criteria.6 months
6-month Progression-free rate (PFR) in patients with non-small cell lung cancer.Progression-free rate is defined as the rate of complete or partial response (CR, PR) or stable disease (SD), as per RECIST 1.1 criteria.6 months
6-month Progression-free rate (PFR) in patients with bladder cancer.Progression-free rate is defined as the rate of complete or partial response (CR, PR) or stable disease (SD), as per RECIST 1.1 criteria.6 months
6-month Progression-free rate (PFR) in patients with triple negative breast cancer.Progression-free rate is defined as the rate of complete or partial response (CR, PR) or stable disease (SD), as per RECIST 1.1 criteria.6 months
6-month objective response rate (ORR) independently for each population.Objective response is defined as the proportion of patients with complete response (CR) or partial response (PR) observed at 6 months, based on RECIST 1.1 criteria.6 months
Objective response rate (ORR) within 24 weeks of treatment onset, independently for each population.Objective response is defined as the proportion of patients with complete response (CR) or partial response (PR) observed within 24 wekks after treatment onset, based on RECIST 1.1 criteria.Within 6 months
Best overall response, independently for each population.Best overall response is defined as the best response across all time points (RECIST 1.1). The best overall response is determined once all the data for the patient is known (RECIST 1.1).Throughout the treatment period, an expected average of 6 months
1-year progression-free survival, independently for each population.Progression-free survival is defined as the delay between the start date of treatment and the date of progression (as per RECIST 1.1) or death (from any cause), whichever occurs first.1 year
2-year progression-free survival, independently for each population.Progression-free survival is defined as the delay between the start date of treatment and the date of progression (as per RECIST 1.1) or death (from any cause), whichever occurs first.2 years
1-year overall survival, independently for each population.Overall survival is defined as the delay between the start date of treatment and the date of death (of any cause).1 year
2-year overall survival, independently for each population.Overall survival is defined as the delay between the start date of treatment and the date of death (of any cause).2 years
Safety profile, independently for each population: Common Terminology Criteria for Adverse Events version 5Toxicity graded using the Common Terminology Criteria for Adverse Events version 5.Throughout the treatment period, an expected average of 6 months
Tumor immune cells levelsLevels of immune cells in tumor will be measured by immunohistochemistry.before treatment onset and cycle 3 day 1 (each cycle is 21 days)
Blood cytokines levelsLevels of cytokines in blood will be measured by ELISA.baseline, cycle 1 day 1, cycle 2 day 1, cycle 3 day 1 and progression (each cycle is 21 days)
Blood lymphocytes levelsLevels of lymphocytes in blood will be measured by flow cytometry.baseline, cycle 1 day 1, cycle 2 day 1, cycle 3 day 1 and progression (each cycle is 21 days)
Blood kynurenine levelsLevels of kynurenine in blood will be measured by ELISA.baseline, cycle 1 day 1, cycle 2 day 1, cycle 3 day 1 and progression (each cycle is 21 days)

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: Antoine ITALIANO, MD, PhD

Phone Number: +33 5.56.33.33.33

Email: a.italiano@bordeaux.unicancer.fr

Study Contact Backup

Name: Simone MATHOULIN-PELISSIER, MD, PhD

Phone Number:

Email: s.mathoulin@bordeaux.unicancer.fr

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion criteria:
    1. histologically confirmed pancreatic cancer, virus-associated tumors [including papillomaviruses-related cancers (cervical, head and neck, and nasal), Epstein-Barr virus (nasopharyngeal carcinoma) and Kaposi's sarcoma-associated herpes virus), non-small cell lung cancer, soft-tissue sarcomas, bladder cancer, triple negative breast cancer. For population 4, diagnosis must be confirmed by the RRePS Network as recommended by the French NCI. For population 2, papillomavirus-related cancers must be eligible whatever the genotype but in case of viral genotype is not available, IHC p16 positive must be provided, hepatocellular carcinoma must be confirmed by Hepatite B or C infection, HHV-8 and Epstein-Barr virus related cancers must be confirmed by molecular analysis, 2. Metastatic disease, 3. Age ≥ 18 years, 4. ECOG ≤ 1, 5. At least two lesions: one extra cerebral lesion that can be treated by radiotherapy and one site of disease that must be uni-dimensionally ≥ 10 mm considered as measurable according to RECIST v1.1. This lesion will not be treated by radiotherapy, however, note that lesion(s) that will be treated by radiotherapy will also be considered as measurable. Note that the largest size of the metastases to be irradiated will be 3cm and at that previous irradiation of these lesions is not allowed, 6. Life expectancy > 6 months, 7. At least one tumor site that can be biopsied for research purpose. Tumor lesion in close proximity to vascular structures such as large vessels, aneurysm or pulmonary arteriovenous malformation will not be considered for biopsy, 8. Availability of archived paraffin-embedded tumor tissue for research purpose, 9. Participant must have advanced disease and must not be a candidate for other approved therapeutic regimen known to provide significant clinical benefit based on investigator judgement, 10. Participants who received prior anti-PD-1/L1 therapy must fulfill the following requirements - population 3 and population 5 only

  • Have achieved a complete response, partial response or stable disease and subsequently had disease progression while still on anti-PD-1/L1 therapy
  • Have received at least two doses of an approved anti-PD-1/L1 therapy (by any regulatory authority)
  • Have demonstrated disease progression as defined by RECIST v1.1 within 18 weeks from the last dose of the anti- PD-1/L1 therapy. 11. Adequate hematological, renal, metabolic and hepatic functions 12. No prior or concurrent malignant disease needing an active treatment, 13. At least three weeks since last chemotherapy, immunotherapy or any other pharmacological treatment and/or radiotherapy, 14. Recovery to grade ≤ 1 from any adverse event (AE) derived from previous treatment, excluding alopecia of any grade and non-painful peripheral neuropathy grade ≤ 2, 15. Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to inclusion. 16. Both women and men must agree to use an effective method of contraception throughout the treatment period and for five months after discontinuation of treatment. 17. Voluntary signed and dated written informed consents prior to any specific study procedure, 18. Participants with a social security in compliance with the French law.

    • Exclusion criteria:
    1. Previous treatment with a TLR agonist 2. Evidence of progressive or symptomatic central nervous system (CNS) or leptomeningeal metastases, 3. Women who are pregnant or breast feeding, 4. Participation in a study involving a medical or therapeutic intervention in the last 30 days, 5. Known hypersensitivity to CHO cell products or to any involved study drug or of its formulation components, 6. History of severe allergic anaphylactic reactions to chimeric, human or humanized antibodies, or fusion proteins, 7. Treatment with systemic immunosuppressive medications including, but not limited to, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-TNF agents within 2 weeks prior to inclusion. 8. Major surgical procedure, open biopsy or significant traumatic injury within 28 days before inclusion, 9. Any of the following cardiac criteria: congestive heart failure ≥ New York Heart Association (NYHA) class 2, unstable angina, new-onset angina, myocardial infarction less than 6 months before inclusion, uncontrolled cardiac arrhythmias, known left ventricular ejection fraction (LVEF) <50%, previously experience of pericardial disorder 10. Individuals deprived of liberty or placed under legal guardianship, 11. Prior organ transplantation, including allogeneic stem cell transplantation, 12. Known clinically significant liver disease, including active viral, alcoholic, or other hepatitis, cirrhosis, fatty liver and inherited liver disease, 13. History of intra-abdominal inflammatory process within the last 12 months such as, but not limited to, diverticulitis, peptic ulcer disease or colitis. 14. History of autoimmune disease including, but not limited to systemic lupus erythematosus (SLE), Sjögren's syndrome, glomerulonephritis, multiple sclerosis, rheumatoid arthritis, vasculitis, systemic immune activation, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Guillain-Barré syndrome, Bell's palsy. 15. History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan. 16. Poorly controlled Type II diabetes mellitus defined as a screening fasting plasma glucose ≥160 mg/dL (or 8.8 mmol/L). 17. Severe infections within 2 weeks prior to inclusion, including but not limited to SARS-Cov-2 infection, hospitalization for complications of infection, bacteremia, or severe pneumonia. 18. Received therapeutic oral or IV antibiotics within 2 weeks prior to inclusion. 19. Participant has spinal cord compression not definitively treated with surgery and/or radiation or previously diagnosed and treated spinal cord compression without evidence that disease is clinically stable at least 14 days prior to inclusion. 20. Administration of a live, attenuated vaccine within 4 weeks before the start of study medication . 21. Has known active hepatitis B or hepatitis C,known history of Human Immunodeficiency or known acquired immunodeficiency syndrome, known history of tuberculosis 22. Patients with current retinal disorder confirmed by retinal examination (external ocular examination, routine slit lamp biomicroscopy of anterior ocular structures and evaluation of the anterior and posterior chamber, 23. Patients who wear contact lenses unable to replace them with glasses.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

  • Roche Pharma AG
  • National Cancer Institute, France
  • Eikon Therapeutics
  • : ,

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available

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