For Healthcare Professionals

Avelumab in First-line NSCLC (JAVELIN Lung 100)

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About the study

The purpose of this study was 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) participants with Programmed death ligand 1+ (PD-L1+) tumors.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Male or female subjects aged greater than or equal to (>=) 18 years
  2. With Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 to 1 at trial entry
  3. At least 1 measurable tumor lesion
  4. With histologically confirmed metastatic or recurrent (Stage IV) non-small cell lung cancer (NSCLC)
  5. 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
  6. Subjects must not have received any treatment for systemic lung cancer, and have an estimated life expectancy of more than 12 weeks
  7. Other protocol defined criteria could apply

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Subjects whose disease harbors a EGFR mutation, or anaplastic lymphoma kinase (ALK) rearrangement are not eligible.
  2. Other exclusion criteria include prior therapy with any antibody or drug targeting T cell coregulatory proteins, concurrent anticancer treatment, or immunosuppressive agents


  3. 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.
  4. 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.
  5. Other protocol defined criteria could apply

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

First Line Non-Small Cell Lung Cancer

Age (in years)

18+

Phase

Phase 3

Participants needed

1214

Est. Completion Date

Jan 31, 2024

Treatment type

Interventional


Sponsor

EMD Serono

ClinicalTrials.gov identifier

NCT02576574

Study number

EMR-100070-005

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