CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 252 enrolled
Drug / intervention
BI 836880 +1 moredrug
Likely dose
Ezabenlimab 240 mgfrom 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/NCT03468426
NCT03468426Phase 1Completed

An Open Label Phase Ib Dose Finding Study of BI 836880 in Combination With Ezabenlimab to Characterize Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy in Patients With Locally Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer and in Other Solid Tumors

Boehringer Ingelheim·interventional·Posted Mar 16, 2018·Updated Nov 10, 2025

In Brief

A Phase 1 clinical trial evaluating BI 836880 and Ezabenlimab for Non-squamous, Non-Small-Cell Lung Cancer and Neoplasms. Completed, enrolled 252 participants across 43 sites in 12 countries.

Detailed Summary

This study has 2 parts. The first part was open to adults with advanced non-small cell lung cancer. The second part was open also to adults with other types of advanced cancer of the lung, brain, skin, and liver. After early encouraging results, more people with liver cancer can now take part in the study. The participants get a combination of two medicines called BI 836880 and ezabenlimab. BI 836880 is a type of an antibody that blocks new blood vessel formation. New blood vessels are needed by the tumour to continue growing. Ezabenlimab is an antibody that may help the immune system fight cancer (immune checkpoint inhibitor). The purpose of the first part of the study was to find out the highest dose of the BI 836880 that the participants can tolerate in combination with BI 754091. After the best dose of BI 836880 for the combination with ezabenlimab was found, it is used in the second part of the study. The purpose of the second part is to see whether the combination of BI 836880 and BI 754091 is able to make tumours shrink. The participants are in the study as long as they benefit from and can tolerate treatment. During this time, they get infusions of BI 836880 and ezabenlimab every 3 weeks. The doctors also regularly check the general health of the participants.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, France, Germany, Hong Kong, Poland, Russia, South Korea, Spain, Taiwan, Ukraine, United Kingdom, United States
Collaborators--

Timeline

Phase 1CompletedFinished
201820192020202120222023202420252026
First PostedMar 16, 2018
Enrollment StartJul 5, 2018
Primary CompletionJul 31, 2024
Study CompletionSep 12, 2024
TodayJul 2, 2026
Enrollment to primary: 6.1 yearsPosted 8.3 years ago

Interventions

BI 836880drug

BI 836880 as an intravenous infusion on day 1 of each 3-week cycle.

Ezabenlimabdrug

240 mg Ezabenlimab (BI 754091) as an intravenous infusion on day 1 of each 3-week cycle.