drugset / Trial / NCT06566443

Honokiol in Early-Stage Resectable Non-Small Cell Lung Cancer

NCT06566443

Phase 1 Recruiting 15 enrolled The Methodist Hospital Research Institute
NaSequentialOpen-labelPrevention

Summary

This is a Phase I Trial evaluating the safety of the dietary supplement honokiol for lung cancer chemoprevention. Female or male patients aged 18 years, or older, with early stage lung cancer who have been scheduled for curative surgery will be eligible for participation in the study. The study will only enroll patients with stage I lung cancers less than 4 cm, given the recent approval of neoadjuvant chemotherapy and nivolumab for stage IB tumors \> 4 cm. Approximately, 15 patients will be enrolled in the study. They will take the study drug, honokiol, for 2 weeks prior to the surgery. The primary endpoint will be the Maximum Tolerated Dose (MTD) of honokiol.

Timeline

Start
2025-02-13
Primary completion
2026-08
Completion
2027-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluoride Other / unclassified 250 mg Oral
Subject Fluoride Other / unclassified 500 mg Oral