drugset / Trial / NCT05800964

Study to Explore the Safety, Tolerability, and Pharmacokinetics of AMG 305 in Subjects With Advanced Solid Tumors

NCT05800964 ↗

Phase 1 Completed 37 enrolled Amgen
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objective of this study is to: * Evaluate the safety and tolerability of AMG 305 in adult participants * Determine the optimal biologically active dose (OBD), at or below the maximum tolerated dose (MTD) with MTD 1 as the maximum tolerated starting dose and MTD 2 as the maximum tolerated target dose * Determine the recommended phase 2 dose (RP2D)

Timeline

Start
2023-06-13
Primary completion
2026-01-22
Completion
2026-01-22

Drugs

EvaluationDrugModalityDoseRoute
Subject AMG 305 Unknown — Intravenous

Indications