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NCT07231575
Neoadjuvant SBRT and Tislelizumab (Immunotherapy) Plus Anlotinib for Resectable EGFR Wild-type NSCLC
Phase 2 trial testing SBRT in Neoadjuvant Immunotherapy in 39 participants. Not yet recruiting.
30 November 2027
Quick facts
| Lead sponsor | Sun Yat-sen University |
|---|---|
| Phase | Phase 2 |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 39 |
| Start date | 10 November 2025 |
| Primary completion | 30 November 2027 |
| Estimated completion | 30 May 2032 |
Drugs / interventions tested
- SBRT — full drug profile →
- Immunotherapy — full drug profile →
- antiangiogenesis therapy — full drug profile →
Conditions studied
- Neoadjuvant Immunotherapy — all drugs for Neoadjuvant Immunotherapy →
- NSCLC — all drugs for NSCLC →
- Chemo-free Therapy — all drugs for Chemo-free Therapy →
Sponsor
Sun Yat-sen University
Who can join
18 and older, any sex, with Neoadjuvant Immunotherapy or NSCLC. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The neoadjuvant strategy of immunotherapy combined with chemotherapy has been recommended for resectable or potentially resectable tumors without driver-gene alterations.However, the AE of chemotherapy is more than 40%,which bring fear to the patients,especially for those who cannot tolerate or refuse chemotherapy.Several studies indicated that the strategies of chemo-free ,such as the combination of immunotherapy with antiangiogenic therapy or with SBRT, were safe and well tolerated, without increasing adverse reactions. Both of them have a promising efficacy with a manageable toxicity profile in patients with resectable NSCLC. The investigators aim to assess the activity and safety of neoadjuvant SBRT and immunotherapy plus antiangiogenic therapy in patients with resectable NSCLC.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07231575
- Europe PMC full search
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Other Sun Yat-sen University trials
Trials by the same sponsor.
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- NCT07528209 — Neoadjuvant CAPOX With or Without Pucotenlimab Plus Selective Radiotherapy for Locally Advanced Rectal Cancer · Phase 3 · recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07231575 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sun Yat-sen University
- Last refreshed: 18 November 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07231575.
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