drugset / Trial / NCT05233436

PF-07265028 As Single Agent And In Combination With Sasanlimab in Advanced or Metastatic Solid Tumors

NCT05233436

Phase 1 Terminated 21 enrolled Pfizer
Non-randomizedSequentialOpen-labelTreatment

Summary

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.

Timeline

Start
2022-02-24
Primary completion
2023-10-16
Completion
2023-10-16

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-07265028 Unknown Oral
Subject Sasanlimab Monoclonal antibody Subcutaneous