Expanded Access Program With Nivolumab Therapy for Treatment of Advanced/Metastatic SqNSCLC or Non-SqNSCLC After One Prior Systemic Regimen (CheckMate 169)
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ClinicalTrials.gov Identifier: NCT02475382 |
Expanded Access Status :
No longer available
First Posted : June 18, 2015
Last Update Posted : November 27, 2020
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Condition or disease | Intervention/treatment |
---|---|
Squamous Non-Small Cell Lung Cancer Non-squamous Non-Small Cell Lung Cancer | Drug: Nivolumab |
Study Type : | Expanded Access |
See clinical trials of the intervention/treatment in this expanded access record. | |
Official Title: | Expanded Access Program With Nivolumab Monotherapy in Subjects With Advanced or Metastatic Squamous (Sq) or Non-Squamous (Non-Sq) Non-Small Cell Lung Cancer (NSCLC) Who Have Received at Least One Prior Systemic Regimens for the Treatment of Stage IIIb/IV SqNSCLC |

- Drug: Nivolumab
Specified dose on specified days

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com
Inclusion Criteria:
- Sq or Non-Sq NSCLC, Stage IIIb/IV (histologically or cytologically confirmed)
- Relapsed after 1 prior platinum-based systemic treatment
- Eastern Cooperative Oncology Group (ECOG) Performance Status < 2
- CNS metastasis must be treated and returned to baseline at least 2 weeks before first dose of nivolumab and off steroids or using stable or decreasing dose of < 10 mg prednisone or equivalent
- Prior chemotherapy, Tyrosine Kinase Inhibitor (TKI) therapy or Immunotherapy (tumor vaccine, cytokine or growth factor to control cancer) must be completed at least 2 weeks before first nivolumab dose
Exclusion Criteria:
- CNS metastases (untreated and/or symptomatic)
- Carcinomatous meningitis
- ECOG Performance status > 3
- Corticosteroids > 10 mg prednisolone/day (or equivalent)
- Prior treatment with anti-PD-1, anti-PD-L-1, anti-PDL2, anti-CT137 or anti-CTLA antibody, including ipilimumab or any other drugs specifically targeting T cell costimulation or checkpoint pathways

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02475382

Study Director: | Bristol-Myers Squibb | Bristol-Myers Squibb |
Responsible Party: | Bristol-Myers Squibb |
ClinicalTrials.gov Identifier: | NCT02475382 |
Other Study ID Numbers: |
CA209-169 |
First Posted: | June 18, 2015 Key Record Dates |
Last Update Posted: | November 27, 2020 |
Last Verified: | November 2020 |
Lung Neoplasms Carcinoma, Non-Small-Cell Lung Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site Neoplasms Lung Diseases Respiratory Tract Diseases |
Carcinoma, Bronchogenic Bronchial Neoplasms Nivolumab Antineoplastic Agents, Immunological Antineoplastic Agents Immune Checkpoint Inhibitors Molecular Mechanisms of Pharmacological Action |