Trials / Not Yet Recruiting
Not Yet RecruitingNCT07365410
Furmonertinib 160mg vs 80mg + Chemotherapy in EGFR-Mutated NSCLC With Brain Metastases: Efficacy and Safety Study
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
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Tianjin Medical University Cancer Institute and Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Furmonertinib | Oral administration, 160mg once daily. |
| DRUG | Furmonertinib | Oral administration, 80mg once daily |
| DRUG | carboplatin | Intravenous infusion, cycle-based (per study protocol). |
| DRUG | pemetrexed | Intravenous infusion, cycle-based (per study protocol). |
Timeline
- Start date
- 2026-01-01
- Primary completion
- 2026-05-01
- Completion
- 2028-12-01
- First posted
- 2026-01-26
- Last updated
- 2026-01-26
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07365410. Inclusion in this directory is not an endorsement.