Fluorescent Imaging of Nerves With Illuminare-1 During Surgery

PHASE1CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

October 4, 2021

Primary Completion Date

September 9, 2025

Study Completion Date

September 9, 2025

Conditions
Prostate Adenocarcinoma
Interventions
DRUG

Illuminare-1

Illuminare-1 at 3 dose levels in patients undergoing minimally invasive radical prostatectomy and bilateral pelvic lymph node dissection. Dose levels of the agent will be administered starting at 0.25mg/kg, with increases in dose between cohorts of no more than 0.75 mg/kg until a maximum dose of 3.0mg/kg is reached, if needed. At the dose identified to have the acceptable NMR and no associated DLTs, Illuminare-1 will be studied in up to 20 additional patients at this dose to optimize the imaging protocol and provide additional safety data.

DEVICE

Karl Storz D-Light C photodynamic diagnostic (PDD)

The Storz PDD system will be used as the hardware system in this phase 1 study due to its proven safety profile.

Trial Locations (6)

10065

Memorial Sloan Kettering Cancer Center, New York

10604

Memorial Sloan Kettering Westchester (Limited protocol activities), Harrison

11725

Memorial Sloan Kettering Cancer Commack (Limited Protocol Activities), Commack

07920

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities), Basking Ridge

07748

Memorial Sloan Kettering Monmouth (Limited protocol activities), Middletown

07645

Memorial Sloan Kettering Bergen (Limited Protocol Activities), Montvale

Sponsors
All Listed Sponsors
collaborator

Illuminare Biotechnologies

UNKNOWN

lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT04983862 - Fluorescent Imaging of Nerves With Illuminare-1 During Surgery | Biotech Hunter | Biotech Hunter