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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

進行固形腫瘍胃がん胃食道接合部がん尿路上皮がん頭頸部扁平上皮癌非小細胞肺がん

介入

PF-07265028(DRUG)
Sasanlimab(BIOLOGICAL)

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