Condition: Peripheral Lung Tumor · Sponsor: Impact Biotech Ltd
Phase 1/1b, safety, feasibility, and light dose titration study followed by further study of therapeutic ablation effects. Patients with high risk of peripheral primary lung cancer, stage 1A1/1A2, for whom surgical treatment is planned, will be recruited. Surgery will be performed at 5-21 days following the VTP procedure. Study intervention: robotic assisted bronchoscopic Padeliporfin VTP lung ablation: vascular targeted photodynamic therapy using Padeliporfin photosensitizer.
This description comes directly from the study's public registry record.
Eyal Morag, MD · +972542056619 · eyal.morag@impactbiotech.com
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| Johns Hopkins University School of Medicine | Baltimore, Maryland, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05918783