PD-1 Inhibitor Plus G-CSF in Recurrent/Metastatic NPC With First-line Treatment Failure
- Sponsor
- Sun Yat-sen University
- Study ID
- NCT05222035
- Phase
- PHASE2
- Status
- Unknown
Conditions
- G-CSF
- PD-1 Inhibitor
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Camrelizumab — DRUGPD-1 inhibitor: Camrelizumab, 200 mg, intravenously (IV) , Day 1, Q3W, until progressive disease (PD) or unacceptable toxicity for a maximum of up to 35 cycles (up to approximately 2 years).
- G-CSF — DRUGG-CSF: mecapegfilgrastim, 6 mg, subcutaneous injection, Day 1, Q3W, until stop using Camrelizumab, progressive disease (PD) or unacceptable toxicity.
Study Details
Recurrence and metastasis are the main causes of treatment failure of NPC. Preliminary clinical studies have found that the overall response rate of PD-1 inhibitors in treating ≥2 line R/M NPC is about 25%. Recent studies have shown that G-CSF can significantly increase the proportion of effector cells dominated by CD4+ T cells, improve the diversity of peripheral blood TCR, and regulate the immune status of patients. Therefore, we suspect that G-CSF may have a synergistic effect on PD-1 inhibitor, thus enhance the efficacy of PD-1 inhibitor monotherapy.
Key Dates
- Start date
- Jan 24, 2022
- Status verified
- Jan 2022
- Primary completion
- Dec 24, 2022
- Completion
- Jun 1, 2023
Study Design
- Enrollment
- 68 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: G-CSF+Camrelizumab
- Active Comparator: Camrelizumab
Primary Outcome Measure
Objective response rate [ Time Frame: 1 year ]
Central Contacts
- Ming-Yuan Chen, MD, PhD02087343392
- Xi Ding, MD86-19880836260