A Study to Learn More About How Well Sevabertinib Works and How Safe it is Compared With Standard Treatment, in Participants Who Have Advanced Non-small Cell Lung Cancer (NSCLC) With Mutations of the Human Epidermal Growth Factor Receptor 2 (HER2)
Public ClinicalTrials.gov record NCT06452277. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 3 Open-label, Randomized, Active-controlled, Multicenter Trial to Evaluate the Efficacy and Safety of Orally Administered BAY 2927088 Compared With Standard of Care as a First-line Therapy in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) With HER2-activating Mutations
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Researchers are looking for a better way to treat people who have advanced non-small cell lung cancer (NSCLC) with specific genetic changes called human epidermal growth factor receptor 2 (HER2) mutations. Advanced NSCLC means lung cancer that has spread nearby or to other parts of the body or is unlikely to be controlled with current treatments. HER2 is a protein that helps cells to grow and divide. Sometimes, cancer cells have a damaged HER2 gene. This is called a mutation. This mutation can lead to an abnormal HER2 protein which may cause cancer cells to grow and divide too quickly. The study treatment, sevabertinib, is designed to block the mutated HER2 protein and may help slow or stop the cancer from growing. The main purpose of this study is to find out how well sevabertinib works and how safe it is, compared with standard treatment in participants with advanced NSCLC with a HER2 mutation. The study participants will receive one of the study treatments: * Sevabertinib as a tablet taken by mouth twice a day * Standard approved treatment for this condition given by infusion into a vein every 21 days Participants will continue their assigned treatment for as long as they benefit from it and do not experience severe side effects, or until they or their doctor decide to stop treatment. When a participant assigned to the standard treatment has their cancer gets worse, they may have the opportunity to switch to receive sevabertinib. This switch is called a crossover. Participants who switch to sevabertinib will continue this treatment until their disease gets worse again, they have side effects that are too severe, or they or their doctor decide to stop treatment. During the study, the research team will: * do scans such as CT, PET, MRI, or X-rays to check the cancer * Check the overall health of the participants by performing tests such as blood and urine tests and checking heart health using an electrocardiogram and echocardiogram. * do pregnancy tests when needed * ask how the participants are feeling and whether they have had any adverse events or other health problems An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events, irrespective if they think it is related or not to the study treatment.
Study identification
- NCT ID
- NCT06452277
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 444 participants
Conditions and interventions
Interventions
- Sevabertinib Drug
- Pembrolizumab Drug
- Cisplatin Drug
- Carboplatin Drug
- Pemetrexed Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 28, 2024 (Actual)
- Primary completion
- Oct 28, 2027 (Estimated)
- Completion
- Jun 27, 2029 (Estimated)
- Last update posted
- Oct 15, 2026
2024 – 2029
United States locations
- U.S. sites
- 25
- U.S. states
- 13
- U.S. cities
- 23
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Patty & George Hoag Cancer Center | Newport Beach | California | 92663 | Withdrawn |
| UC San Diego Health - Moores Cancer Center | San Diego | California | 92037 | Withdrawn |
| UCSF Bakar Precision Cancer Medicine Building - Thoracic Surgery and Oncology | San Francisco | California | 94158 | Recruiting |
| UCLA Health Santa Monica Cancer Care | Santa Monica | California | 90404 | Recruiting |
| The Oncology Institute of Hope and Innovation - Fort Lauderdale 17th Street | Fort Lauderdale | Florida | 33316 | Recruiting |
| Memorial Cancer Institute at Miramar | Miramar | Florida | 33029 | Completed |
| AdventHealth Cancer Institute Orlando | Orlando | Florida | 32804 | Not yet recruiting |
| Moffitt Cancer Center - Magnolia Campus | Tampa | Florida | 33612 | Withdrawn |
| Piedmont Healthcare - Atlanta | Atlanta | Georgia | 30318 | Recruiting |
| John B. Amos Cancer Center | Columbus | Georgia | 31904 | Recruiting |
| University of Illinois Hospital - Outpatient Cancer Care Center | Chicago | Illinois | 60612 | Recruiting |
| The University of Chicago Medical Center - Hyde Park - Hematology & Oncology | Chicago | Illinois | 60637 | Withdrawn |
| UM Greenebaum Comprehensive Cancer Center | Baltimore | Maryland | 21201 | Not yet recruiting |
| UMass Memorial Medical Center - University Campus - Hematology/Oncology | Worcester | Massachusetts | 01655 | Withdrawn |
| Profound Research -OMG - TriAtria Cancer Center | Farmington Hills | Michigan | 48334 | Withdrawn |
| Profound Research - OMG - Royal Oak Cancer Center | Royal Oak | Michigan | 48073 | Withdrawn |
| M Health Fairview Masonic Cancer Clinic - Clinics and Surgery Center | Minneapolis | Minnesota | 55455 | Withdrawn |
| R.J. Zuckerberg Cancer Center | New Hyde Park | New York | 11042 | Withdrawn |
| UC Medical Center - Oncology | Cincinnati | Ohio | 45219 | Recruiting |
| Taylor Cancer Research Center | Maumee | Ohio | 43537 | Recruiting |
| Providence Cancer Institute - Franz Clinic | Portland | Oregon | 97213 | Not yet recruiting |
| Providence Oncology and Hematology Care Clinic Westside | Portland | Oregon | 97225 | Not yet recruiting |
| Allegheny General Hospital | Pittsburgh | Pennsylvania | 15212 | Recruiting |
| University Hospital Simmons Cancer Center Lung/Head Neck Clinic | Dallas | Texas | 75235 | Withdrawn |
| The University of Texas MD Anderson Cancer Center - Texas Medical Center | Houston | Texas | 77030 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 254 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06452277, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 15, 2026 · Synced Oct 17, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT06452277 live on ClinicalTrials.gov.