Avelumab in First-line Non-Small Cell Lung Cancer (JAVELIN Lung 100)
Status: | Active, not recruiting |
---|---|
Conditions: | Lung Cancer, Lung Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/6/2019 |
Start Date: | October 29, 2015 |
End Date: | June 3, 2025 |
A Phase III, Open-label, Multicenter Trial of Avelumab (MSB0010718C) Versus Platinum-based Doublet as a First-line Treatment of Recurrent or Stage IV PD-L1+ Non-small Cell Lung Cancer
The purpose of this study is to demonstrate superiority with regard to Overall Survival (OS)
or Progression Free Survival (PFS) of avelumab versus platinum-based doublet, based on an
Independent Review Committee assessment, in Non-small cell lung cancer (NSCLC) subjects with
Programmed death ligand 1+ (PD-L1+) tumors
or Progression Free Survival (PFS) of avelumab versus platinum-based doublet, based on an
Independent Review Committee assessment, in Non-small cell lung cancer (NSCLC) subjects with
Programmed death ligand 1+ (PD-L1+) tumors
Inclusion Criteria:
- Male or female subjects aged greater than or equal to (>=) 18 years
- With Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 to 1 at
trial entry
- At least 1 measurable tumor lesion
- With histologically confirmed metastatic or recurrent (Stage IV) non-small cell lung
cancer (NSCLC)
- With availability of a recently-obtained, formalin-fixed, paraffin-embedded (FFPE)
tissue sample containing tumor (biopsy from a non-irradiated area preferably within 6
months) or a minimum number of 10 (preferably 25) unstained tumor slides cut within 1
week, and suitable for PD-L1 expression assessment
- Subjects must not have received any treatment for systemic lung cancer, and have an
estimated life expectancy of more than 12 weeks
- Other protocol defined criteria could apply
Exclusion Criteria:
- Subjects whose disease harbors a EGFR mutation, or anaplastic lymphoma kinase (ALK)
rearrangement are not eligible.
- Other exclusion criteria include prior therapy with any antibody or drug targeting T
cell coregulatory proteins, concurrent anticancer treatment, or immunosuppressive
agents
- Known severe hypersensitivity reactions to monoclonal antibodies (Grade >= 3 NCI CTCAE
v 4.03), history of anaphylaxis, or uncontrolled asthma (that is, 3 or more features
of partially controlled asthma), and persisting toxicity related to prior therapy of
Grade > 1 NCI-CTCAE v 4.03.
- Subjects with brain metastases are excluded, except those meeting the following
criteria: brain metastases that have been treated locally and are clinically stable
for at least 2 weeks prior to randomization, subjects must be either off steroids or
on a stable or decreasing dose of <= 10 mg daily prednisone (or equivalent), and do
not have ongoing neurological symptoms that are related to the brain localization of
the disease.
- Other protocol defined criteria could apply
We found this trial at
21
sites
Cookeville, Tennessee 38501
Principal Investigator: Paul Jacquin
Phone: 931-783-2476
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201 Borella Road
Albury, New South Wales 2640
Albury, New South Wales 2640
Principal Investigator: Richard Eek
Phone: +61260641498
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Boynton Beach, Florida 33426
Principal Investigator: Thomas Niederman
Phone: 561-737-6556
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Henry Ford Hospital Founded in 1915 by auto pioneer Henry Ford and now one of...
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1915 White Ave.
Knoxville, Tennessee 37916
Knoxville, Tennessee 37916
(865) 541-1678

Principal Investigator: Samuel McCachren
Phone: 865-541-4985
Thompson Cancer Survival Center The Thompson Cancer Survival Center Downtown facility has pioneered many advances...
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Lancaster, Pennsylvania 17601
Principal Investigator: Hyatt Peter DeGreen
Phone: 717-291-1313
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Oklahoma City, Oklahoma 73120
Principal Investigator: James Reeves
Phone: 405-752-3402
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Portland, Oregon 97227
Principal Investigator: Nagendra Tirumali
Phone: 503-249-3506
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Sharp Memorial Hospital Sharp Memorial Hospital offers clinical excellence with the latest technology and patient-centered...
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Surprise, Arizona 85374
Principal Investigator: Clarence Adoo
Phone: 602-938-2848
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