Recruiting
Phase 3

Zongertinib vs. Standard Treatment

Sponsor:

Boehringer Ingelheim

Code:

NCT07195695

Conditions

Non-small Cell Lung Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Zongertinib

Pembrolizumab

Atezolizumab

Durvalumab

Nivolumab

Study Details

Brief summary:

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.

Conditions

Non-small Cell Lung Cancer

Study ID

NCT07195695

Start date

Jan 16, 2026

Status verified date

Sep, 2026

Completion date

Sep 2, 2036

Anticipated

Primary completion date

Feb 26, 2032

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

400 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Zongertinib treatment arm

active comparator: Standard of Care (SoC) treatment arm

Interventions

Zongertinib

Zongertinib

Pembrolizumab

Pembrolizumab

Atezolizumab

Atezolizumab

Durvalumab

Durvalumab

Nivolumab

Nivolumab

Primary outcome measure

  • Disease-free survival (DFS) by investigator's assessment [ Time Frame: up to 8 years and 5 months ]

Central Contacts and Locations

Central contacts

Locations

ClinRé 001-022 (Premier Cancer Care and Infusion Center)

Recruiting

Fresno, California, United States, 93710

Contacts

OPN Healthcare, Inc.

Recruiting

Glendale, California, United States, 91203

Contacts

University of California San Francisco

Recruiting

San Francisco, California, United States, 94158

Contacts

Sarcoma Oncology Center

Recruiting

Santa Monica, California, United States, 90403

Contacts

University of California Los Angeles

Recruiting

Santa Monica, California, United States, 90404

Contacts

Mid Florida Hematology and Oncology Center

Recruiting

Orange City, Florida, United States, 32763

Contacts

Piedmont Cancer Institute

Recruiting

Atlanta, Georgia, United States, 30318

Contacts

Northwest Georgia Oncology Centers

Recruiting

Marietta, Georgia, United States, 30060

Contacts

University of Illinois Hospital and Health Sciences System

Recruiting

Chicago, Illinois, United States, 60612

Contacts

Duly Health and Care - Lisle

Recruiting

Lisle, Illinois, United States, 60532

Contacts

Dana-Farber Cancer Institute

Recruiting

Boston, Massachusetts, United States, 02215

Contacts

Cancer Care Specialists

Recruiting

Reno, Nevada, United States, 89511

Contacts

Laura & Isaac Perlmutter Cancer Center at NYU Langone Health

Recruiting

New York, New York, United States, 10016

Contacts

Memorial Sloan-Kettering Cancer Center

Recruiting

New York, New York, United States, 10065

Contacts

Providence Cancer Institute

Recruiting

Portland, Oregon, United States, 97213

Contacts

Hendrick Health

Recruiting

Abilene, Texas, United States, 79601

Contacts

Community Cancer Trials of Utah

Recruiting

Ogden, Utah, United States, 84405

Contacts

Virginia Cancer Specialists, PC

Recruiting

Fairfax, Virginia, United States, 22031

Contacts

More Information

Sponsor

Boehringer Ingelheim

Last update posted

Sep 3, 2026

Last verified

Sep, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Boehringer Ingelheim on 2026-09-03.