A Phase II, Multicenter, Single-Arm Study of MPDL2380A in Patients With PD-L1-Positive Locally Advanced or Metastatic Non-Small Cell Lung Cancer
This multicenter, single-arm study will evaluate the efficacy and safety of MPDL3280A in
patients with PD-L1-positive locally advanced or metastatic non-small cell lung cancer.
Patients will receive MPDL3280A 1200 mg intravenously every 3 weeks as long as patients are
experiencing clinical benefit as assessed by the investigator, i.e., in the absence of
unacceptable toxicity or symptomatic deterioration attributed to disease progression.
View more details from ClinicalTrials.gov.
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Please Note: Any eligibility criteria noted are subject to change. Our research nurses can provide you with the most current eligibility and exclusion criteria. Any study involvement to be undertaken must ultimately be determined on an individual basis.