drugset / Trial / NCT06131398

A Study of AMG 355 Alone and in Combination With Pembrolizumab in Participants With Advanced Solid Tumors

NCT06131398 ↗

Phase 1 Active not recruiting 77 enrolled Amgen
Non-randomizedSequentialOpen-labelBasic science

Summary

The primary objectives of this study are to: * Evaluate the safety and tolerability of AMG 355 as monotherapy and in combination with pembrolizumab in participants with advanced solid tumors * Determine the recommended phase 2 dose and the maximum tolerated dose for AMG 355 as monotherapy and in combination with pembrolizumab in participants with advanced solid tumors.

Timeline

Start
2024-03-07
Primary completion
2026-07-21
Completion
2026-07-21

Drugs

EvaluationDrugModalityDoseRoute
Subject AMG 355 Unknown — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous

Indications