Trials / Unknown
UnknownNCT06334757
Serplulimab Plus Bevacizumab and Chemotherapy for EGFR-mutant Metastatic NSCLC Patients After EGFR-TKI Treatment Failure
A Multi-center, Open-label, Single-arm Study to Evaluate the Efficacy and Safety of Serplulimab Plus Bevacizumab and Chemotherapy for EGFRm+ Locally Advanced or Metastasis Non-Squamous NSCLC Patients After EGFR-TKI Treatment Failure
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 46 (estimated)
- Sponsor
- Henan Cancer Hospital · Other Government
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy and safety of Serplulimab Plus Bevacizumab and chemotherapy in TKI-resistant EGFR-mutated non-squamous NSCLC Chinese patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Serplulimab | 300 mg,IV,Q3W |
| DRUG | Bevacizumab Biosimilar HLX04 | 7.5 mg/kg,Q3W |
| DRUG | Pemetrexed | 500 mg/m2,IV,Q3W |
| DRUG | Carboplatin | AUC=5,IV,Q3W |
Timeline
- Start date
- 2023-05-08
- Primary completion
- 2024-08-31
- Completion
- 2025-06-30
- First posted
- 2024-03-28
- Last updated
- 2024-03-28
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06334757. Inclusion in this directory is not an endorsement.