Non-small Cell Lung Cancer (NSCLC)Phase 2NCT07365410
Furmonertinib 160mg vs 80mg + Chemotherapy in EGFR-Mutated NSCLC With Brain Metastases: Efficacy and Safety Study
A Phase 2 study testing Furmonertinib, carboplatin and pemetrexed in people with Non-small Cell Lung Cancer (NSCLC) and Brain Metastases, run by Tianjin Medical University Cancer Institute and Hospital at 1 site in China.
Trial summary
This multicenter study evaluates the efficacy and safety of furmonertinib 160mg versus furmonertinib 80mg plus chemotherapy (carboplatin + pemetrexed) as first-line treatment for EGFR-mutated NSCLC patients with brain metastases. It aims to determine which approach is more effective and safer. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Non-small Cell Lung Cancer (NSCLC), Brain Metastases, Furmonertinib
- What is being tested?
- Furmonertinib, carboplatin and pemetrexed
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteChina
- Study dates
- Jan 2026to Dec 2028
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
IInclusion Criteria
- Aged 18 to 75 years (male or female)
- Histopathologically confirmed, unresectable, and non-radiocurable newly -diagnosed locally advanced or metastatic lung adenocarcinoma
- Confirmed by local laboratory to have one of the following EGFR mutations: -19Del or L858R (single or mixed mutations are allowed)
- Treatment-naive for locally advanced (not suitable for surgery/radiotherapy per investigator) or metastatic NSCLC; adjuvant/neoadjuvant therapy completed >6 months before first progression is allowed (≤6 months is considered pretreated)
- At least one measurable tumor lesion per RECIST 1.1 (lesions previously treated with radiotherapy are excluded; if only one measurable lesion exists, biopsy is allowed but baseline imaging must be performed ≥14 days after biopsy)
- Confirmed stable and asymptomatic brain metastases
- Sufficient organ function (per laboratory tests): ANC ≥1.5×10⁹/L, PLT ≥100×10⁹/L, HGB ≥90g/L; TBIL ≤1.5×ULN, AST/ALT ≤2.5×ULN (for liver metastasis: TBIL ≤3×ULN, AST/ALT ≤5×ULN); CrCL ≥50 ml/min (Cockcroft-Gault formula)
- ECOG performance status 0-2 (no significant disease deterioration in 2 weeks before screening)
- Expected survival >12 weeks after first dose
- Non-pregnant women of childbearing potential (no pregnancy plan); women and men agree to use effective contraception during the study and 6 months after drug discontinuation
- Voluntarily signs informed consent and understands the study procedures Exclusion Criteria(排除标准)
- NSCLC with predominantly squamous cell histology, small cell lung cancer, neuroendocrine carcinoma, or other non-adenocarcinoma histologies
- Concurrent positive for other driver genes (ALK fusion, ROS1 fusion, RET rearrangement, BRAF mutation, NTRK fusion, MET mutation, KRAS mutation); TP53, RB1, and BRAC mutations are excluded
- Expected to receive other anti-tumor therapies during the trial
- Major surgery (except vascular access or biopsy) within 4 weeks before first dose or planned during the trial
- Use of CYP3A4 strong inhibitor within 7 days or strong inducer within 21 days before first dose; use of anti-tumor Chinese medicine within 2 weeks before first dose or planned during the trial
- Participation in other clinical trials (investigational drug/device) within 4 weeks or 5 half-lives before first dose
- Use of other anti-tumor drugs within 14 days before first dose
- Spinal cord compression or symptomatic leptomeningeal metastasis
- Toxicity from previous anti-tumor therapy not recovered to ≤CTCAE Grade 1 (except alopecia or platinum-induced peripheral neuropathy)
- Symptomatic or unstable pleural/peritoneal effusion (stable ≥14 days after drainage is allowed)
- History of other malignancies (except cured malignancies with no recurrence in 5 years: cervical carcinoma in situ, basal cell carcinoma, papillary thyroid carcinoma)
- History of interstitial lung disease (ILD), drug-induced ILD, steroid-requiring radiation pneumonitis, or suspected ILD
- Uncontrolled severe systemic diseases (e.g., hypertension, diabetes, NYHA III-IV heart failure, unstable angina, myocardial infarction within 1 year, active bleeding)
- QTc >470 msec on resting ECG
- Clinically significant QT prolongation or arrhythmias increasing QT risk (e.g., complete left bundle branch block, III° AV block, congenital long QT syndrome, severe hypokalemia, use of drugs causing QT prolongation)
- Severe gastrointestinal dysfunction that impairs drug intake or absorption Infections requiring intravenous medication
- Active mental illness or drug addiction
- Known or suspected allergy to furmonertinib or its components
- Pregnant or lactating women; women or their partners planning pregnancy during the study
- Poor compliance (unable to follow study procedures)
- Other conditions deemed unsuitable for enrollment by the investigator
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site
Tianjin Medical University Cancer Institute and Hospital
Tianjin
Dingzhi Huang Huang, +86-22-23340123-1031, dingzhih72@163.com
About this study
Official title: Furmonertinib 160mg Versus Furmonertinib 80mg Combined With Chemotherapy (Carboplatin + Pemetrexed) as First-Line Treatment for EGFR-Mutated NSCLC Patients With Brain Metastases: A Multicenter Study of Efficacy and Safety
This multicenter study evaluates the efficacy and safety of furmonertinib 160mg versus furmonertinib 80mg plus chemotherapy (carboplatin + pemetrexed) as first-line treatment for EGFR-mutated NSCLC patients with brain metastases. It aims to determine which approach is more effective and safer.
- Being tested
- Furmonertinib, carboplatin, pemetrexed
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung, Brain Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FurmonertinibDrug
Oral administration, 160mg once daily.
FurmonertinibDrug
Oral administration, 80mg once daily
carboplatinDrug
Intravenous infusion, cycle-based (per study protocol).
pemetrexedDrug
Intravenous infusion, cycle-based (per study protocol).
| Study group | Role | What they receive |
|---|---|---|
| Furmonertinib 160mg Group | Experimental | Participants receive oral furmonertinib 160mg once daily as first-line treatment. Receives: Drug: Furmonertinib |
| Furmonertinib 80mg + Chemotherapy Group | Active comparator | Participants receive oral furmonertinib 80mg once daily combined with intravenous carboplatin + pemetrexed (cycle-based) as first-line treatment. Receives: Drug: Furmonertinib; Drug: carboplatin; Drug: pemetrexed |
What is being measured
The primary outcome is the main question the study is designed to answer.
Median Progression-Free Survival (PFS) as assessed by Investigator
The time from the first dose of the study drug to the progression of the disease (Investigator-Assessed) or death for any reason according to investigator.
Measured: Approximately 18 months after the first patient begin study treatment
Secondary outcomes (9)
Objective Response Rate (ORR) as assessed by RECIST 1.1
Proportion of subjects whose tumors were assessed as complete response(CR) or partial response(PR) according to RECIST 1.1.
Measured: Approximately 12 weeks following the first dose of study drug
Disease Control Rate (DCR) as assessed by RECIST 1.1
Proportion of subjects whose tumors were assessed as CR, PR or stable disease (SD) according to RECIST 1.1.
Measured: Approximately 18 months from the first patient begin study treatment
Central Nervous System (CNS) Objective Response Rate (CNS ORR) as assessed by RECIST 1.1
Proportion of subjects whose central nervous system (CNS) tumors (including intracranial parenchymal metastases and asymptomatic meningeal metastases as defined in the inclusion criteria) are assessed as Complete Response (CR) or Partial Response (PR) according to RECIST1.1.
Measured: Approximately 12 weeks after the first dose of study drug
Central Nervous System (CNS) Disease Control Rate (CNS DCR) as assessed by RECIST 1.1
Proportion of subjects whose central nervous system (CNS) tumors (including intracranial parenchymal metastases and asymptomatic meningeal metastases as defined in the inclusion criteria) are assessed as Complete Response (CR), Partial Response (PR), or Stable Disease (SD) according to RECIST 1.1.
Measured: Approximately 18 months after the first dose of study drug
Central Nervous System Progression-Free Survival (CNS PFS) as assessed by RECIST 1.1
The time from the first dose of the study drug (Furmonertinib) to the first occurrence of central nervous system (CNS) disease progression (assessed by RECIST 1.1) or death from any cause, whichever comes first.
Measured: Approximately 18 months after the first dose of study drug
Median Overall Survival (OS)
The time from the first does of the study drugs to the death for any reason
Measured: Approximately 24 months after the first dose of study drug
Safety Profile (Adverse Events, AE) as assessed by CTCAE v5.0
The number of patients with adverse events and the severity grading (Grade 1-5) according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Measured: From the start of study drug to 28 days after the last dose of study drug
Progression Pattern as assessed by RECIST 1.1 and Clinical Evaluation
Proportion of subjects with first disease progression classified as Intracranial, extracranial, or combined intracranial-extracranial progression.
Measured: Approximately 18 months after the first dose of study drug
Site Analysis of Disease Progression as assessed by RECIST 1.1 and Clinical Evaluation
Frequency of specific progression sites.
Measured: Approximately 18 months after the first dose of study drug
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jan 2026
- Study startJan 2026 (estimated)
- Primary completionMay 2026 (estimated)
- Study completionDec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-small Cell Lung Cancer (NSCLC)Studies of the same condition, open and under way.
- More trials run by Tianjin Medical University Cancer Institute and HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07365410
- Sponsor's protocol ID
- E20250722
- Status last verified
- Nov 2025
- First submitted
- 26 Nov 2025
- Last updated
- 26 Jan 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data (IPD) to be shared include demographic characteristics, clinical baseline data (e.g., ECOG PS score, EGFR mutation status, brain metastasis status), efficacy endpoints (median PFS, ORR, DCR, CNS ORR, CNS DCR, CNS PFS, OS) assessed by RECIST 1.1, adverse event data graded by CTCAE v5.0, progression pattern and site data, and biomarker (NGS) data collected at baseline and disease progression. The data will be made available after the completion of the primary analysis (expected by December 2028) for non-commercial scientific research purposes, to support further exploration of EGFR-mutated NSCLC with brain metastasis treatment.
Study at a glance
From the registry record, last updated by the sponsor on 26 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Furmonertinib 160mg Versus Furmonertinib 80mg Combined With Chemotherapy (Carboplatin + Pemetrexed) as First-Line Treatment for EGFR-Mutated NSCLC Patients With Brain Metastases: A Multicenter Study of Efficacy and Safety
- ClinicalTrials.gov ID
- NCT07365410
- Acronym / sponsor ID
- E20250722
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Tianjin Medical University Cancer Institute and HospitalUniversity, hospital or other
- Study start
- Jan 2026 (estimated)
- Primary completion
- May 2026 (estimated)
- Study completion
- Dec 2028 (estimated)
- First posted
- 26 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This multicenter study evaluates the efficacy and safety of furmonertinib 160mg versus furmonertinib 80mg plus chemotherapy (carboplatin + pemetrexed) as first-line treatment for EGFR-mutated NSCLC patients with brain metastases. It aims to determine which approach is more effective and safer.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Furmonertinib 160mg Group | Experimental | Drug: FurmonertinibParticipants receive oral furmonertinib 160mg once daily as first-line treatment. |
| Furmonertinib 80mg + Chemotherapy Group | Active comparator | Drug: Furmonertinib, Drug: carboplatin, Drug: pemetrexedParticipants receive oral furmonertinib 80mg once daily combined with intravenous carboplatin + pemetrexed (cycle-based) as first-line treatment. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| FurmonertinibOral administration, 160mg once daily. | Drug | Furmonertinib 160mg Group |
| FurmonertinibOral administration, 80mg once daily | Drug | Furmonertinib 80mg + Chemotherapy Group |
| carboplatinIntravenous infusion, cycle-based (per study protocol). | Drug | Furmonertinib 80mg + Chemotherapy Group |
| pemetrexedIntravenous infusion, cycle-based (per study protocol). | Drug | Furmonertinib 80mg + Chemotherapy Group |
Primary outcome
Median Progression-Free Survival (PFS) as assessed by Investigator
Time frame: Approximately 18 months after the first patient begin study treatment
The time from the first dose of the study drug to the progression of the disease (Investigator-Assessed) or death for any reason according to investigator.
9 secondary outcomes
Objective Response Rate (ORR) as assessed by RECIST 1.1
Time frame: Approximately 12 weeks following the first dose of study drug
Disease Control Rate (DCR) as assessed by RECIST 1.1
Time frame: Approximately 18 months from the first patient begin study treatment
Central Nervous System (CNS) Objective Response Rate (CNS ORR) as assessed by RECIST 1.1
Time frame: Approximately 12 weeks after the first dose of study drug
Central Nervous System (CNS) Disease Control Rate (CNS DCR) as assessed by RECIST 1.1
Time frame: Approximately 18 months after the first dose of study drug
Central Nervous System Progression-Free Survival (CNS PFS) as assessed by RECIST 1.1
Time frame: Approximately 18 months after the first dose of study drug
Median Overall Survival (OS)
Time frame: Approximately 24 months after the first dose of study drug
Safety Profile (Adverse Events, AE) as assessed by CTCAE v5.0
Time frame: From the start of study drug to 28 days after the last dose of study drug
Progression Pattern as assessed by RECIST 1.1 and Clinical Evaluation
Time frame: Approximately 18 months after the first dose of study drug
Site Analysis of Disease Progression as assessed by RECIST 1.1 and Clinical Evaluation
Time frame: Approximately 18 months after the first dose of study drug
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Jan 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data (IPD) to be shared include demographic characteristics, clinical baseline data (e.g., ECOG PS score, EGFR mutation status, brain metastasis status), efficacy endpoints (median PFS, ORR, DCR, CNS ORR, CNS DCR, CNS PFS, OS) assessed by RECIST 1.1, adverse event data graded by CTCAE v5.0, progression pattern and site data, and biomarker (NGS) data collected at baseline and disease progression. The data will be made available after the completion of the primary analysis (expected by December 2028) for non-commercial scientific research purposes, to support further exploration of EGFR-mutated NSCLC with brain metastasis treatment.
Related trials for Non-small Cell Lung Cancer (NSCLC)
RecruitingPhase 1/2
Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)
Solid Tumor, Non-Small Cell Lung Cancer
RecruitingObservational study
A Prospective ,Multicenter ,Non-interventional ,Real-world Study Observing Changes in Molecular Markers Osimertinib Targeted Therapy in EGFRm NSCLC
Non Small Cell Lung Cancer
RecruitingPhase 3
A Study Evaluating Sotorasib Platinum Doublet Combination Versus Pembrolizumab Platinum Doublet Combination as a Front-Line Therapy in Participants With Stage IV or Advanced Stage IIIB/C Nonsquamous Non-Small Cell Lung Cancers (CodeBreaK 202)
Non-Small Cell Lung Cancer (NSCLC)
Active, not recruitingPhase 2
Datopotamab Deruxtecan (Dato-DXd, DS-1062a) in Advanced and/or Unresectable Non-Small Cell Lung Cancer
Metastatic Lung Cancer, Advanced Non Small Cell Lung Cancer
Not yet recruitingPhase 1/2
STAR0602 With Nivolumab in Non Small Cell Lung Cancer and in Metastatic Castrate-Resistant Prostate Cancer, and STAR0602 Alone in Thymic Carcinoma
NSCLC, Non-Small Cell Lung Cancer
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Furmonertinib, carboplatin and pemetrexed in people with Non-small Cell Lung Cancer (NSCLC) and Brain Metastases, run by Tianjin Medical University Cancer Institute and Hospital at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 26 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Dingzhi Huang Huang (+86-22-23340123-1031, dingzhih72@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Median Progression-Free Survival (PFS) as assessed by Investigator (time frame: Approximately 18 months after the first patient begin study treatment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jan 2026.