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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.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

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
What is being tested?
Furmonertinib, carboplatin and pemetrexed
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.

Dingzhi Huang Huang contact

+86-22-23340123-1031

dingzhih72@163.com

China1 site
  • Tianjin Medical University Cancer Institute and Hospital

    Tianjin

    Dingzhi Huang Huang, +86-22-23340123-1031, dingzhih72@163.com

Other trials in China

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 groups in NCT07365410
Study groupRoleWhat they receive
Furmonertinib 160mg GroupExperimentalParticipants receive oral furmonertinib 160mg once daily as first-line treatment.
Receives: Drug: Furmonertinib
Furmonertinib 80mg + Chemotherapy GroupActive comparatorParticipants 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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.

  1. First posted26 Jan 2026
  2. Study startJan 2026 (estimated)
  3. Primary completionMay 2026 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

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)
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.

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.

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