drugset / Trial / NCT05661201

NEROFE and Doxorubicin in KRAS-mutated ST2-positive Solid Tumors

NCT05661201 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

The goal of this clinical trial is to learn about the safety of NEROFE and doxorubicin and how well it works in patients with advanced/unresectable or metastatic solid KRAS-mutated and ST-positive solid tumors. The main question it aims to answer is to find the recommended dose and scheduled for the combination of NEROFE and doxorubicin. Participants will receive weekly doses of NEROFE and doxorubicin.

Timeline

Start
2023-04-12
Primary completion
2027-01
Completion
2027-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Doxorubicin Other / unclassified 8 mg/m2 Intravenous
Subject Nerofe Peptide 48 mg/m2 Intravenous
Subject Nerofe Peptide 96 mg/m2 Intravenous
Subject Nerofe Peptide 192 mg/m2 Intravenous
Subject Nerofe Peptide 288 mg/m2 Intravenous

Indications