Nivolumab and Epacadostat With Platinum Doublet Chemotherapy Versus Platinum Doublet Chemotherapy in Non-Small Cell Lung Cancer
Status: | Terminated |
---|---|
Conditions: | Lung Cancer, Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/7/2019 |
Start Date: | December 27, 2017 |
End Date: | May 22, 2018 |
A Phase 3, Randomized, Global Trial of Nivolumab and Epacadostat With Platinum Doublet Chemotherapy Versus Platinum Doublet Chemotherapy in First-line Treatment of Stage IV or Recurrent Non-Small Cell Lung Cancer (NSCLC)
The purpose of this study is to evaluate the efficacy and safety of the combination of
nivolumab plus epacadostat in combination with platinum chemotherapy compared with platinum
chemotherapy alone, in participants with treatment-naïve Stage 4 or recurrent non-small cell
lung cancer (NSCLC).
nivolumab plus epacadostat in combination with platinum chemotherapy compared with platinum
chemotherapy alone, in participants with treatment-naïve Stage 4 or recurrent non-small cell
lung cancer (NSCLC).
Inclusion Criteria:
- Histologically confirmed stage IV or recurrent NSCLC of squamous or non-squamous
histology that is not amenable to therapy with curative intent (surgery or radiation
therapy with or without chemotherapy).
- No prior treatment with systemic anti-cancer therapy for Stage IV disease.
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to1.
- Measurable disease by computed tomography or magnetic resonance imaging per RECIST
v1.1.
- Documentation of program death ligand-1 (PD-L1) status of 0 to 49% by IHC performed by
the central laboratory prior to randomization.
- Other protocol inclusion criteria may apply
Exclusion Criteria:
- Known epidermal growth factor receptor (EGFR) mutations sensitive to available
targeted inhibitor therapy.
- Known ALK or ROS1 rearrangements sensitive to available targeted inhibitor therapy.
- Untreated central nervous system (CNS) metastases.
- Unevaluable PD-L1 status or PD-L1 status of ≥ 50% by IHC performed by a central
laboratory.
- Carcinomatous meningitis.
- Active, known or suspected autoimmune disease.
- Prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4 antibody, IDO1
targeted agent, or any other antibody or drug targeting T cell co-stimulation or
checkpoint pathways.
- History of allergy or hypersensitivity to platinum-containing compounds or study drug
components.
- Physical and laboratory test findings outside the protocol-defined range.
- Other protocol exclusion criteria may apply.
We found this trial at
2
sites
Cancer Center of Kansas The physicians of Cancer Center are hematologists and oncologists. The staff...
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