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Beamion LUNG-3: Adjuvant Zongertinib vs Standard Treatment in People With Completely Resected Stage II-IIIB NSCLC Harboring Activating HER2 TKD Mutations

RecruitingPhase 3

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion criteria:

1. Signed and dated written informed consent in accordance with ICH-GCP and local legislation prior to admission to the trial
2. Patients must be ≥18 years old or over the legal age of consent in their country
3. Male or female patients. Women of childbearing potential (WOCBP) must be ready and able to use dual highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly. A list of contraception methods meeting these criteria is provided in the patient information and in the study protocol
4. HER2 mutation: Documented Tyrosine kinase domain (TKD) activating Human epidermal growth factor receptor 2 (HER2) mutations
5. Histology and tumor sample: Histologically confirmed diagnosis of primary NSCLC
6. An archival tumor tissue sample must be submitted to the central laboratory after inclusion of the patient to retrospectively confirm the HER2 status
7. Staging: Pretherapeutic classification not exceeding Stage IIIB
8. Performance status and organ function:

   * Eastern Cooperative Oncology Group (ECOG) score of 0 or 1
   * Adequate organ function based on laboratory values Further inclusion criteria apply.

Exclusion criteria:

1. Diagnosis of NSCLC with mixed histology/positive neuroendocrine markers (synaptophysin/CD56)
2. Major surgery (major according to the investigator's assessment) performed within 4 weeks prior to randomization
3. Treatment with radiation therapy for primary NSCLC
4. Co-occurring actionable mutation with approved targeted therapy (e.g. Epidermal growth factor receptor (EGFR) or Anaplastic lymphoma kinase (ALK))
5. Any investigational drug within 5 half-lives of the compound or any of its related material, if known
6. History or presence of

   * Active or known pre-existing or history of non-infectious interstitial lung disease/pneumonitis
   * Active infectious disease requiring systemic therapy
   * Uncontrolled gastrointestinal disorders affecting drug intake/absorption
   * Previous or concomitant malignancies within the last 3 years, except certain effectively treated cancers
   * Significant and/or uncontrolled cardiovascular abnormalities, QT interval corrected for heart rate by Fridericia formula (QTcF) \>470 msec, or ejection fraction \<50% Further exclusion criteria apply.

About the study

Beamion LUNG-3 study evaluates whether zongertinib, an oral HER2-targeted treatment, can improve outcomes compared with standard adjuvant treatment in adults with completely resected Stage II-IIIB non-small cell lung cancer (NSCLC) whose tumors have activating HER2 tyrosine kinase domain (TKD) mutations. Eligible participants must have undergone curative-intent surgery and received guideline-appropriate perioperative systemic therapy, either neoadjuvant platinum-based chemotherapy with or without immunotherapy, or adjuvant platinum-based chemotherapy.

Participants are randomized 1:1 to receive zongertinib or standard of care, which may consist of approved adjuvant immunotherapy or active surveillance, based on local practice guidelines. The main purpose of the study is to determine whether zongertinib can prolong disease-free survival compared to standard treatment. Safety and patient-reported outcomes are also assessed.

What is being tested

Sponsor: Boehringer Ingelheim · Participants: 400 · Started: Jan 16, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07195695

Locations in the U.S.

CaliforniaClinRé 001-022 (Premier Cancer Care and Infusion Center), Fresno
OPN Healthcare, Inc., Glendale
University of California Irvine, Orange
Sutter Health, Roseville (Not yet recruiting)
University of California San Francisco, San Francisco
Sarcoma Oncology Center, Santa Monica
University of California Los Angeles, Santa Monica
Northern California Kaiser Permanente, Vallejo (Not yet recruiting)
District of ColumbiaGeorge Washington University Cancer Center, Washington D.C. (Not yet recruiting)
FloridaMid Florida Hematology and Oncology Center, Orange City
GeorgiaPiedmont Cancer Institute, Atlanta
Northwest Georgia Oncology Centers, Marietta
IdahoSaint Alphonsus Regional Medical Center - Boise, Boise (Not yet recruiting)
IllinoisNorthwestern University, Chicago (Not yet recruiting)
University of Illinois Hospital and Health Sciences System, Chicago
Duly Health and Care - Lisle, Lisle
MassachusettsDana-Farber Cancer Institute, Boston
NevadaCancer Care Specialists, Reno
New YorkLaura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York
Memorial Sloan-Kettering Cancer Center, New York
North CarolinaLevine Cancer Institute, Charlotte (Not yet recruiting)
Durham VA Health Care System, Durham (Not yet recruiting)
OregonProvidence Cancer Institute, Portland
TexasHendrick Health, Abilene
The University of Texas MD Anderson Cancer Center, Houston (Not yet recruiting)
UtahCommunity Cancer Trials of Utah, Ogden
VirginiaVirginia Cancer Specialists, PC, Fairfax

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.