Sintilimab Combination Therapy Plus IMRT in Nasopharyngeal Carcinoma
- Disease/Condition
- Nasopharyngeal Carcinoma
- Drug/Device/Intervention
- Sintilimab, bevacizumab, gemcitabine
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Zhejiang Cancer Hospital
- Phase
- Phase 2
- Start date
- Apr 22, 2024
- End date
- Apr 22, 2026
- Enrollment
- 60 participants
3-year Event-free survival rate
This is a prospective, single-center, single-arm, phase II clinical study. The study was
 intended to include patients with locoregionally advanced nasopharyngeal cancer identified by
 histology or cytology, who signed informed consent and met the screening criteria to enter
 the study. Patients will receive induction therapy (sintilimab + bevacizumab + gemcitabine,
 Q3W, 3 cycles) followed by IMRT+ Sintilimab. Consolidation therapy with sintilimab continued
 after radiotherapy until disease progression, intolerable toxicity, death, or the subject's
 decision to withdraw from the study, with a total treatment period of no more than 12 cycles.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06364826
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06364826 through Pure Global AI's free database. This Phase 2 trial is sponsored by Zhejiang Cancer Hospital and is currently Not yet recruiting. The study focuses on Nasopharyngeal Carcinoma. Target enrollment is 60 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.