Ivonescimab in Neoadjuvant NSCLC: Testing a PD-1/VEGF Bi-specific
Official title: Mechanisms of Enhanced Efficacy of Ivonescimab in Neoadjuvant Therapy for Non-Small Cell Lung Cancer
Run by Peking University People's Hospital · NCT07359040 · Data updated 2026-11-12
This study tests Ivonescimab, a PD-1/VEGF bispecific antibody, in people with non-small cell lung cancer to see if it works better or has different safety than standard PD-1 inhibitors before surgery.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Peking University People's Hospital Academic / other |
| Drugs / interventions | Ivonescimab, immunotherapy |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Status | Recruiting |
| Started | July 1, 2025 |
| Main results expected | December 21, 2026 |
| Study ends | October 30, 2027 |
| Registry record updated | June 3, 2026 |
| Trial ID | NCT07359040 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with stage IB-IIIB NSCLC who require radical surgery after neoadjuvant therapy.
✕Probably not a fit
Patients with unresectable disease, non-NSCLC histologies, or contraindications to neoadjuvant therapy may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study compares Ivonescimab with conventional PD-1 inhibitors when used as neoadjuvant therapy for NSCLC. It aims to explore not only efficacy and safety but also the mechanisms behind Ivonescimab’s potential enhanced effect. Secondary analyses include biomarker identification and multi-omics profiling to understand predictors of response and the drug’s molecular action in the tumor microenvironment. The work intends to support precision medicine strategies and rational clinical use of Ivonescimab in resectable NSCLC. The study is conducted at Peking University People’s Hospital in Beijing, China.
Why it matters
Potential benefit: If successful, Ivonescimab could offer improved tumor response prior to surgery and personalized treatment approaches for NSCLC.
How similar studies have gone: Early research on PD-1/VEGF bispecific antibodies suggests potential benefits, but results are still exploratory and context-dependent.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Patients with non-small cell lung cancer (Stage IB-IIIB) who require radical surgery following neoadjuvant therapy. Exclusion Criteria: 1. Histology of other malignant tumors, including concurrent malignant tumors of other organ systems; 2. Unresectable advanced disease (Stage IV) or locally advanced unresectable (Stage IIIC); 3. Pregnancy or lactation; 4. Insufficient sample quality; 5. Severe organ dysfunction (e.g. cardiac or renal insufficiency); 6. Other judgments by the Investigator that the patient should not participate in the study.
Where it's running
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Peking University People's Hospital
Beijing, Beijing Municipality, China Recruiting
Study contacts
- Principal investigator: Fan Yang — Peking University People's Hospital
- Study coordinator: Hao Li
- Email: lihao_pkuhsc@163.com
- Phone: +86 13051713494
Similar studies
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Tepotinib plus Ivonescimab for MET exon 14–positive NSCLC
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Ivonescimab after SBRT for early-stage NSCLC
This study tests whether adding ivonescimab after standard SBRT helps people with early-stage non-small cell lung cancer.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.