A Phase II Clinical Study of SHR-1826 for Injection in Patients With NSCLC
- Sponsor
- Suzhou Suncadia Biopharmaceuticals Co., Ltd.
- Study ID
- NCT06844474
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- SHR-1826;Adebrelimab;SHR-8068;Bevacizumab — DRUGDrug: Drug: SHR-1826 Administration by intravenous infusion for a cycle of 3 weeks. Drug: Adebrelimab Administration by intravenous infusion for a cycle of 3 weeks. Drug: SHR-8068 Administration by intravenous infusion for a cycle of 6 weeks. Drug: Bevacizumab Administration by intravenous infusion for a cycle of 3 weeks.
Study Details
This study is an open-label, multicenter Phase II clinical trial to evaluate the safety, tolerability and efficacy of SHR-1826 for injection in patients with NSCLC.
Key Dates
- First listed
- Feb 25, 2025
- Start date
- Mar 7, 2025
- Status verified
- Feb 2025
- Primary completion
- Aug 31, 2026
- Completion
- Feb 29, 2028
Study Design
- Enrollment
- 300 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm ASHR-1826 for injection in combination with Adebrelimab injection and SHR-8068 with or without Bevacizumab injection
Primary Outcome Measure
Incidence and severity of adverse events (AEs) /serious adverse events(SAEs) [ Time Frame: approximately 2 years ]
Central Contacts
- Li Song0518-82342973
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