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再発性・転移性嗅神経芽腫:ニボルマブの有効性と安全性の評価
基本情報
- NCT ID
- NCT07100704
- ステータス
- 募集中
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 14
- 治験依頼者名
- National Cancer Center Hospital East
概要
This trial evaluates the efficacy and safety of nivolumab monotherapy in patients with recurrent or metastatic olfactory neuroblastoma that is difficult to treat with curative intent. Specifically, nivolumab 240 mg will be administered on Day 1 and Day 15 of each cycle, or nivolumab 480 mg will be administered on Day 1 of each cycle, and this will be continued until disease progression. One cycle is 28 days. The decision on which treatment to administer will be made through consultation between the participant in this trial and their attending physician.
対象疾患
Recurrent/ Metastatic Olfactory Neuroblastoma
介入
Nivolumab(DRUG)
依頼者(Sponsor)
実施施設 (2)
自治医科大学附属病院
Shimotsuke, Tochigi, Japan(RECRUITING)
国立研究開発法人国立がん研究センター中央病院
Kashiwa, Chiba, Japan(RECRUITING)