A Clinical Study of T3011 in Combination With PD-1/PD-L1 Inhibitors in Subjects With Advanced Solid Tumors
- Disease/Condition
- Advanced Solid Tumors
- Drug/Device/Intervention
- T3011 high dose
- Study type
- Interventional
- Intervention type
- biological
- Primary sponsor
- Shanghai Pharmaceuticals Holding Co., Ltd
- Location
- Anyang,Bengbu,Changsha,Chengdu,Dongwan,Fuzhou,Guangzhou,Guangzhou,Ha'erbin,Hangzhou,Hangzhou,Jinan,Nanchang,Nanning,Shanghai,Shanghai,Shenyang,Shenzhen,Taiyuan,Tianjin,Wuhan,Zhengzhou, China
- Phase
- Phase 1/2
- Start date
- Jan 11, 2024
- End date
- May 31, 2026
- Enrollment
- 68 participants
Incidence of Treatment-Emergent Adverse Events,Objective response rate(ORR)
This clinical study evaluated the efficacy and safety of T3011 in combination with PD-1/PD-L1
 inhibitors in subjects with advanced solid tumors
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06214143
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06214143 through Pure Global AI's free database. This Phase 1/2 trial is sponsored by Shanghai Pharmaceuticals Holding Co., Ltd and is currently Recruiting. The study focuses on Advanced Solid Tumors. Target enrollment is 68 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.