PF-07265028 進行性または転移性固形腫瘍における単剤およびササンリマブとの併用
基本情報
- NCT ID
- NCT05233436
- ステータス
- 中止
- 試験のフェーズ
- 第1相
- 試験タイプ
- 介入
- 目標被験者数
- 21
- 治験依頼者名
- Pfizer
概要
The purpose of this study is to assess the safety and effects of PF-07265028 as monotherapy and in combination with sasanlimab. The study aims to identify the maximum tolerated dose (MTD) of PF-07265028 as monotherapy; evaluate the clinical activity of monotherapy and combination; and select the recommended dose of PF-07265028 monotherapy and in combination for potential further studies and development. The study contains 2 parts, Dose Escalation (Part 1) to determine the recommended dose of PF-07265028 as single agent and in combination, followed by Dose Expansion (Part 2) in selected tumor types at the recommended dose. It is expected that most participants will take part in this study for up to 1 year with six on-site visits in the first month and then at least twice every subsequent month while they are on treatment.
対象疾患
介入
依頼者(Sponsor)
実施施設 (3)
公益財団法人がん研究会 有明病院
Koto, Tokyo, Japan
The Cancer Institute Hospital of JFCR
Koto, Tokyo, Japan
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