Apatinib Combined With SHR-1210 Injection in the Treatment of Patients With Removable IB-IIIA NSCLC
- Sponsor
- Sichuan Cancer Hospital and Research Institute
- Study ID
- NCT04133337
- Phase
- PHASE1/PHASE2
- Status
- Unknown
Conditions
- Lung Diseases
- Neoplasms
- Non-small-cell Lung Cancer
- Respiratory Tract Diseases
- Thoracic Neoplasms
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib — DRUGApatinib Mesylate Tablets
- SHR-1210 — DRUGCamrelizumab for Injection
Study Details
The aim of this study was to investigate the safety and efficacy of SHR-1210 in combination with the anti-vascular survival target drug apatinib in patients with resectable NSCLC, and to provide new treatment options for neoadjuvant therapy in patients with the period IB-IIIA NSCLC.
Key Dates
- Start date
- Nov 1, 2019
- Status verified
- Oct 2019
- Primary completion
- Jun 1, 2020
- Completion
- Jun 30, 2021
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib Combined With SHR-1210 Injection* Drugs:Apatinib Apatinib mesylate tablets 250 mg qd po, discontinued one week before surgery. * Drugs: SHR-1210 SHR-1210 injection 200mg (5mL), ivgtt, q2w, 3 cycles, each time 20-60min completed infusion. * Surgery: The patient underwent imaging examinations within 7 days prior to surgery, including chest CT and related metastatic examinations. The patient underwent surgery 7-8 weeks after the first dose.
Primary Outcome Measure
Major pathologic response rate(MPR)(<10% viable tumor cells) [ Time Frame: At time of surgery ]
Central Contacts
- Juan Li, MD+8613880276636
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