Camrelizumab Combined with Apatinib Mesylate Tablets, Nab-paclitaxel and S-1 in the Treatment of Locally Advanced Gastric Cancer
- Sponsor
- Fujian Medical University
- Study ID
- NCT04195828
- Phase
- PHASE2
- Status
- Completed
Conditions
- Advanced Gastric Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Camrelizumab — DRUGCamrelizumab One course will last 21 days.Given once every 3 weeks at a dose of 200 mg.
- Apatinib Mesylate — DRUGApatinib One course will last 21 days.Oral administration at a dose of 250 mg everyday。
- nab-paclitaxel — DRUGnab-paclitaxel One course will last 21 days。Given twice every 3 weeks at a dose of 125 mg/m2.
- S1 — DRUGS-1 was calculated according to body surface area , P.O., bid, d1-d14。And the dosage according body surface area:\<1.25m2, 40mg every time;1.25-1.5m2,50mg every time; \>1.5m2, 60mg every time
Study Details
To evaluate the clinical efficacy and safety of camrelizumab combined with apatinib mesylate, nab-paclitaxel and S-1
Key Dates
- Start date
- Jun 18, 2020
- Status verified
- Mar 2025
- Primary completion
- Jul 22, 2022
- Completion
- Mar 24, 2025
Study Design
- Enrollment
- 106 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Camrelizumab + Apatinib + nab-paclitaxel +S-1Camrelizumab combined with Apatinib mesylate tablets, nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer
- Active Comparator: nab-paclitaxel +S-1nab-paclitaxel and S-1 in the treatment of locally advanced gastric cancer
Primary Outcome Measure
major pathological response [ Time Frame: 4 months ]
Related Studies
- A Study of Disitamab Vedotin With Other Anticancer Drugs in Solid TumorsPHASE2 · Recruiting · Seagen, a wholly owned subsidiary of Pfizer · Tucson, Arizona