CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 472 enrolled
Drug / intervention
Nivolumab +8 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01454102
NCT01454102Phase 1Completed

A Multi-arm Phase I Safety Study of Nivolumab in Combination With Gemcitabine/Cisplatin, Pemetrexed/Cisplatin, Carboplatin/Paclitaxel, Bevacizumab Maintenance, Erlotinib, Ipilimumab or as Monotherapy in Subjects With Stage IIIB/IV Non-small Cell Lung Cancer (NSCLC)

Bristol-Myers Squibb·interventional·Posted Oct 18, 2011·Updated Oct 12, 2021

In Brief

A Phase 1 clinical trial evaluating Nivolumab, Gemcitabine, and 7 other interventions for Non-small Cell Lung Cancer. Completed, enrolled 472 participants across 12 sites in 2 countries.

Detailed Summary

* The study is evaluating the safety and tolerability of Nivolumab (BMS-936558) when combined with three platinum-based doublet chemotherapy regimens (Cisplatin/Gemcitabine; Cisplatin/Pemetrexed; and Carboplatin/Paclitaxel) in subjects with NSCLC. * The study is evaluating the safety and tolerability of Nivolumab as maintenance therapy in combination with Bevacizumab/Avastin that will be given after at least 4 cycles of platinum doublet chemotherapy. * The study is evaluating the safety and tolerability of Nivolumab in combination with Erlotinib among epidermal growth factor receptor (EGFR) mutation positive non-squamous NSCLC subjects and as monotherapy in subjects with NSCLC. * The study is evaluating the safety and tolerability of Nivolumab in combination with Ipilimumab in subjects with squamous and non-squamous NSCLC. * The study is evaluating the safety and tolerability of Nivolumab as switch maintenance therapy in subjects with squamous and non-squamous NSCLC. * The study is evaluating the safety and tolerability of Nivolumab as monotherapy among subjects with untreated, asymptomatic brain metastases and no evidence of cerebral edema.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

Phase 1CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedOct 18, 2011
Enrollment StartDec 16, 2011
Primary CompletionJul 20, 2016
Study CompletionJul 23, 2021
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 14.7 years ago

Interventions

Nivolumabbiological

Gemcitabinedrug

Cisplatindrug

Pemetrexeddrug

Paclitaxeldrug

Carboplatindrug

Bevacizumabdrug

Erlotinibdrug

Ipilimumabbiological