drugset / Trial / NCT05835609

PM534 Administered Intravenously to Patients With Advanced Solid Tumors

NCT05835609 ↗

Phase 1 Recruiting 30 enrolled PharmaMar
NaSequentialOpen-labelTreatment

Summary

The goals of this trial are to identify the dose limiting toxicities, to determine the maximum tolerated dose and the recommended dose of PM534 in patients with advanced solid tumors. All Patients will receive PM534 via intravenous.

Timeline

Start
2022-12-23
Primary completion
2026-10
Completion
2026-10

Drugs

EvaluationDrugModalityDoseRoute
Subject PM534 Unknown — Intravenous

Indications

No indication recorded.