drugset / Trial / NCT04362748

Study of AMG 256 in Adult Subjects With Advanced Solid Tumors

NCT04362748 ↗

Phase 1 Completed 34 enrolled Amgen
Non-randomizedSequentialOpen-labelTreatment

Summary

To evaluate the safety and tolerability of AMG 256 in adult participants and to determine the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D).

Timeline

Start
2020-09-15
Primary completion
2023-09-21
Completion
2023-09-21

Drugs

EvaluationDrugModalityDoseRoute
Subject LATIKAFUSP Protein / enzyme biologic — Intravenous

Indications