This study intends to describe the real-life effectiveness and safety of nivolumab in
advanced NSCLC patients in Germany, as well as the patient profile, pattern of use and the
quality of life.
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Locations near you
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Full eligibility criteria for NCT02910999
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Histologically or cytologically confirmed diagnosis of locally advanced or metastatic NSCLC, Stage IIIB/Stage IV
Decision to initiate a treatment with Nivolumab for the first time already undertaken by physician
Males and Females, ≥18 years of age
Current primary diagnosis of a cancer other than advanced NSCLC. Example: A cancer other than NSCLC that requires systemic or other treatment.
Pre-treatment with Nivolumab and/or Ipilimumab (pre-treatment with checkpoint-inhibitors other than Nivolumab and Ipilimumab, and Tyrosine Kinase Inhibitors(TKIs) is allowed)
Current participation in an interventional clinical trial for treatment of NSCLC.
(Patients who have completed their participation in an interventional trial or who are not receiving study drug anymore and who are only followed-up for overall survival can be enrolled. For blinded studies, the treatment administered needs to be known) Other protocol defined inclusion/exclusion criteria could apply
All locations for NCT02910999
Frankfurt, Germany, 60590
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Tris trial is registered with FDA with number: NCT02910999. The sponsor of the trial is Bristol-Myers Squibb and it is looking for 1000 volunteers for the current phase.
Official trial title: A National, Prospective, Non-Interventional Study (NIS) of Nivolumab (BMS-936558) In Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Squamous and Non-Squamous Histology (Stage IIIB/IV) After Prior Chemotherapy
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