drugset / Trial / NCT06526819

SMP-3124LP in Adults With Advanced Solid Tumors

NCT06526819 ↗

Phase 1/2 Recruiting 120 enrolled Sumitomo Pharma America, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

An Open-label, Phase I Dose Escalation and Phase 2 Dose Expansion Study to Assess Safety, Tolerability, Preliminary Antitumor Activity of SMP 3124LP in Adults with Advanced Solid Tumors

Timeline

Start
2024-08-14
Primary completion
2028-12
Completion
2029-05

Drugs

EvaluationDrugModalityDoseRoute
Subject SMP-3124 Unknown 20 mg/m2 Intravenous
Subject SMP-3124 Unknown 40 mg/m2 Intravenous
Subject SMP-3124 Unknown 60 mg/m2 Intravenous
Subject SMP-3124 Unknown 90 mg/m2 Intravenous
Subject SMP-3124 Unknown 120 mg/m2 Intravenous

Indications