A Study to Learn More About How Well Sevabertinib (BAY 2927088) 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)
- Conditions
- Advanced Non-small Cell Lung CancerHER2 Mutation
- Interventions
- Registration Number
- NCT06452277
- Lead Sponsor
- Bayer
- Brief Summary
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 is a group of lung cancers that have spread to nearby tissues or to other parts of the body or that are unlikely to be cured or controlled with currently available treatments. HER2 is a protein that helps cells to grow and divide. A damage (also called mutation) to the building plans (genes) for this protein in cancer cells leads to a production of abnormal HER2 and therefore abnormal cell growth and division.
The study treatment, BAY 2927088, is expected to block the mutated HER2 protein which may stop the spread of NSCLC.
The main purpose of this study is to learn how well BAY 2927088 works and how safe it is compared with standard treatment, in participants who have advanced NSCLC with specific genetic changes called HER2 mutations.
The study participants will receive one of the study treatments:
* BAY 2927088 twice every day as a tablet by mouth, or
* Standard treatment in cycles of 21 days via infusion ("drip") into the vein. The treatment will continue for as long as participants benefit from it without any severe side effects or until they or their doctor decide to stop the treatment.
During the study, the doctors and their study team will:
* take imaging scans, including CT, PET, MRI, and X-rays, of different parts of the body to study the spread of cancer
* check the overall health of the participants by performing tests such as blood and urine tests, and checking
* heart health using an electrocardiogram (ECG)
* perform pregnancy tests for women
* ask the participants questions about how they are feeling and what adverse events they are having.
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 278
- Participant must be ≥18 years of age or over the legal age of consent in countries where that is greater than 18 years at the time of signing the informed consent.
- Documented histologically or cytologically confirmed locally advanced non-squamous NSCLC, not suitable for definitive therapy or metastatic non-squamous NSCLC at screening (small cell or mixed histologies are excluded) (Stage III-IV NSCLC).
- Documented activating HER2 mutation in the tyrosine kinase domain (TKD) assessed by tissue molecular test in a CLIA-certified (US sites) or an equally accredited (outside of the US) local laboratory. However, participants may be included at the discretion of the investigator if the laboratory performing the assay is not CLIA or similar certified but the laboratory is locally accredited.
- No prior systemic therapy for locally advanced or metastatic disease. No prior treatment with a HER2 ex20ins-targeted therapy (e.g. poziotinib, trastuzumab deruxtecan). Participants who received adjuvant or neoadjuvant therapy are eligible if the adjuvant/neoadjuvant therapy was completed at least 12 months prior to the start of screening.
- Eligible to receive treatment with the selected platinum-based doublet-chemotherapy (i.e. cisplatin/pemetrexed or carboplatin/pemetrexed) and pembrolizumab in accordance with the SmPC/Product Information.
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Known history of prior malignancy except if the participant has undergone potentially curative therapy with no evidence of that disease recurrence for five years since initiation of that therapy. Exception: the following cancer types are acceptable within five years if curatively treated or under surveillance:
- a. in situ cancers of cervix, breast, or skin,
- b. superficial bladder cancer (Ta, Tis and T1),
- c. limited-stage prostate cancer,
- d. basal or squamous cancers of the skin.
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Tumors with targetable alterations with approved available therapy, with the exception of HER2 mutation in the TKD.
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Inability to discontinue treatment with chronic systemic corticosteroids. Participants who require intermittent use of bronchodilators, inhaled steroids, or local steroid injections would not be excluded from the study. Replacement therapy (e.g., physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is acceptable, provided that the dose is stable for >4 weeks prior to planned start of study intervention.
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Pre-existing peripheral neuropathy that is Grade ≥2 by CTCAE (v5.0).
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History of severe hypersensitivity reaction to treatment with a monoclonal antibody.
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Prior radiotherapy outside of the brain within 21 days before of planned start of study intervention. Participants must have recovered from all radiation-related toxicities and not require corticosteroids.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Standard of care (SoC) Pembrolizumab Participants will receive SoC (pembrolizumab in combination with platinum-based chemotherapy, in 21-day cycles per the approved labels) until disease progression per RECIST v1.1, unacceptable toxicity, or until any other withdrawal criteria. Standard of care (SoC) Cisplatin Participants will receive SoC (pembrolizumab in combination with platinum-based chemotherapy, in 21-day cycles per the approved labels) until disease progression per RECIST v1.1, unacceptable toxicity, or until any other withdrawal criteria. Standard of care (SoC) Carboplatin Participants will receive SoC (pembrolizumab in combination with platinum-based chemotherapy, in 21-day cycles per the approved labels) until disease progression per RECIST v1.1, unacceptable toxicity, or until any other withdrawal criteria. Standard of care (SoC) Pemetrexed Participants will receive SoC (pembrolizumab in combination with platinum-based chemotherapy, in 21-day cycles per the approved labels) until disease progression per RECIST v1.1, unacceptable toxicity, or until any other withdrawal criteria. BAY2927088 BAY2927088 Participants will receive BAY2927088 20 mg BID until disease progression per RECIST v1.1, unacceptable toxicity, or until any other withdrawal criteria.
- Primary Outcome Measures
Name Time Method Progression free survival (PFS) per RECIST 1.1 as assessed by BICR Up to approximately 2 years RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1; BICR = blinded independent central review (BICR)
- Secondary Outcome Measures
Name Time Method Overall survival (OS) Up to approximately 4 years. Objective response rate (ORR) per RECIST 1.1 as assessed by BICR Up to approximately 4 years RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1; BICR = blinded independent central review (BICR)
Progression free survival (PFS) per RECIST 1.1 as assessed by the investigator Up to approximately 4 years RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1
Objective Response Rate (ORR) per RECIST 1.1 as assessed by the investigator Up to approximately 4 years Disease control rate (DCR) per RECIST 1.1 as assessed by BICR Up to approximately 4 years RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1; BICR = blinded independent central review (BICR)
Disease control rate (DCR) per RECIST 1.1 as assessed by the investigator Up to approximately 4 years RECIST 1.1 = Response Evaluation Criteria in Solid Tumors, version 1.1
Duration of response (DOR) as assessed by BICR Up to approximately 4 years BICR = blinded independent central review (BICR)
Duration of response (DOR) as assessed by the investigator Up to approximately 4 years Adverse events per CTCAE v 5.0 (eg. TEAEs, TESAEs) categorized by severity Up to approximately 4 years CTCAE = common terminology criteria for adverse events; TEAE = treatment-emergent adverse event; TESAE = treatment-emergent serious adverse event
Change from baseline in NSCLC-SAQ total score Up to approximately 4 years NSCLC-SAQ = Non-small cell lung cancer Symptom Assessment Questionnaire
Change from baseline in NSCLC-SAQ individual domain scores Up to approximately 4 years NSCLC-SAQ = Non-small cell lung cancer Symptom Assessment Questionnaire; Domains: cough, pain, dyspnea, fatigue, appetite
Time to deterioration in NSCLC-SAQ total score Up to approximately 4 years NSCLC-SAQ = Non-small cell lung cancer Symptom Assessment Questionnaire
Time to deterioration in NSCLC-SAQ individual domain scores Up to approximately 4 years NSCLC-SAQ = Non-small cell lung cancer Symptom Assessment Questionnaire; Domains: cough, pain, dyspnea, fatigue, appetite
Time to deterioration in EORTC QLQ-C30 physical functioning domain score Up to approximately 4 years EORTC QLQ-C30: European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30
Change from baseline in EORTC QLQ-C30 physical functioning domain score Up to approximately 4 years EORTC QLQ-C30: European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30; QoL: quality of life
Change from baseline in EORTC QLQ-C30 global health status/QoL Up to approximately 4 years EORTC QLQ-C30: European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30; QoL: quality of life
Trial Locations
- Locations (277)
Patty & George Hoag Cancer Center
🇺🇸Newport Beach, California, United States
UC San Diego Health - Moores Cancer Center
🇺🇸San Diego, California, United States
UCSF Bakar Precision Cancer Medicine Building - Thoracic Surgery and Oncology
🇺🇸San Francisco, California, United States
UCLA Health Santa Monica Cancer Care
🇺🇸Santa Monica, California, United States
The Oncology Institute of Hope and Innovation - Fort Lauderdale 17th Street
🇺🇸Fort Lauderdale, Florida, United States
Memorial Cancer Institute at Miramar
🇺🇸Miramar, Florida, United States
AdventHealth Cancer Institute
🇺🇸Orlando, Florida, United States
Moffitt Cancer Center - Magnolia Campus
🇺🇸Tampa, Florida, United States
Moffitt Cancer Center
🇺🇸Tampa, Florida, United States
Piedmont Cancer Institute - Atlanta
🇺🇸Atlanta, Georgia, United States
Scroll for more (267 remaining)Patty & George Hoag Cancer Center🇺🇸Newport Beach, California, United States