drugset / Trial / NCT07839819

Study of PM54 in Combination With Cytotoxic and Targeted Agents in Adult Participants With Advanced Malignancies

NCT07839819 ↗

Phase 1/2 Not yet recruiting 231 enrolled PharmaMar
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the safety, tolerability and recommended dose (RD) of PM54 in combination with cytotoxic and targeted anticancer agents in adult participants with advanced solid tumors. The study will also assess the antitumor activity of PM54 in combination with cytotoxic and targeted anticancer agents in terms of objective response rate (ORR) based on investigator's assessment in participants in other cohorts.

Timeline

Start
2026-11-12
Primary completion
2029-09-27
Completion
2029-11-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Doxorubicin Other / unclassified — Intravenous
Subject Irinotecan Small molecule — Intravenous
Subject PM54 Unknown — Intravenous

Indications