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Beamion LUNG-3: A Randomized, Controlled, Multi-center Trial Evaluating Zongertinib as an Adjuvant Monotherapy Compared With Standard of Care in Patients With Early-stage, Resectable Non-small Cell Lung Cancer (Stage II-IIIB) Harboring Tyrosine Kinase Domain Activating HER2 Mutations
This study is open to adults 18 years and older who have early-stage non-small cell lung cancer (NSCLC). Their cancer must have a specific change in a gene called HER2. Genes provide the instructions for making proteins, and this change leads to a faulty HER2 protein. People can join if their lung cancer was removed by surgery, and they have already received certain other anti-cancer treatments. The purpose of this study is to find out if a study medicine called zongertinib helps people with this type of cancer live longer without their cancer coming back after surgery, when compared to standard treatment. Zongertinib is being developed to target the faulty HER2 protein, which can cause cancer cells to grow. In this study, participants are assigned by chance to one of two treatment groups, with an equal chance of being in either group. One group takes the study medicine, zongertinib, by mouth once a day for up to 3 years. The other group receives a standard treatment, chosen by their doctor. This standard treatment may be an immunotherapy medicine given by infusion into a vein every 3 or 4 weeks for up to 1 year, or regular check-ups without active study medicine (observation). Participants can be in this study for up to about 11 years. During this time, they visit the study site regularly for check-ups and study-related tests. The frequency of these visits varies depending on their treatment and how long they have been in the study. In addition to visits at the study site, participants in some treatment groups will also have phone calls with the study team every 3 weeks to check on their health between their scheduled visits. Doctors check for any signs of cancer coming back using imaging scans (like CT or MRI scans); these scans are generally done every 3 months for the first 2 years, then every 6 months for the next 3 years, and then yearly. Participants also fill in questionnaires about their overall wellbeing, health and symptoms. Throughout the study, doctors also check participants' health and note any unwanted effects.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
ClinRé 001-022 (Premier Cancer Care and Infusion Center)
Fresno, California, United States
OPN Healthcare, Inc.
Glendale, California, United States
Sutter Health
Roseville, California, United States
Sarcoma Oncology Center
Santa Monica, California, United States
University of California Los Angeles
Santa Monica, California, United States
Northern California Kaiser Permanente
Vallejo, California, United States
George Washington University Cancer Center
Washington D.C., District of Columbia, United States
Mid Florida Hematology and Oncology Center
Orange City, Florida, United States
Piedmont Cancer Institute
Atlanta, Georgia, United States
Northwest Georgia Oncology Centers
Marietta, Georgia, United States
Start Date
January 16, 2026
Primary Completion Date
February 26, 2032
Completion Date
September 2, 2036
Last Updated
March 18, 2026
400
ESTIMATED participants
Zongertinib
DRUG
Pembrolizumab
DRUG
Atezolizumab
DRUG
Durvalumab
DRUG
Nivolumab
DRUG
Lead Sponsor
Boehringer Ingelheim
NCT06305754
NCT07190248
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07100080