Perioperative Treatment of Combined SOX With Apatinib and Camrelizumab for Oesophagogastric Cancer
- Sponsor
- Ruijin Hospital
- Study ID
- NCT04208347
- Phase
- PHASE2/PHASE3
- Status
- Active Not Recruiting
Conditions
- Gastric and Gastroesophageal Junction (GEJ) Adenocarcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib 250mg — DRUGApatinib 250mg
- Camrelizumab — DRUGCamrelizumab 200mg
- S-1, Oxaliplatin — DRUGS-1, Oxaliplatin, q3w
- Apatinib 500mg — DRUGApatinib 500mg
Study Details
The study is being conducted to evaluate the efficacy, safety and tolerability of chemotherapy and apatinib with or without camrelizumab in the neoadjuvant (prior to surgery) or adjuvant (after surgery) treatment of previously untreated adults with gastric and gastroesophageal junction (GEJ) adenocarcinoma.
Key Dates
- Start date
- Dec 18, 2019
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 580 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib and Camrelizumab and S-1 and Oxaliplatin
- Experimental: Apatinib and S-1 and Oxaliplatin
- Active Comparator: S-1 and Oxaliplatin
Primary Outcome Measure
Pathological Complete Response (pCR) [ Time Frame: Up to 6 weeks after completion of 3 cycles (each cycle is 21 days) of neoadjuvant treatment ]
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