Prostatic Hyperplasia Clinical Trial
Official title:
A Phase II Randomized, Sham-Controlled, Double-Blind, Dose-Finding Study to Assess the Efficacy and Safety of Transurethral Photodynamic Therapy With Lemuteporfin in Subjects With Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia
The purpose of this study is to determine if transurethral photodynamic therapy with
lemuteporfin has a therapeutic effect on lower urinary tract symptoms due to an enlarged
prostate.
Photodynamic therapy (known as "PDT") is a treatment that uses light to make a drug work.
This means the drug is "light-activated". Light-activated drugs do not work until a certain
color of light shines on the drug. When the drug and the light combine, they react together
to destroy tissue.
This study is investigating PDT with lemuteporfin as a possible treatment for an enlarged
prostate. PDT with lemuteporfin may destroy overgrown prostate tissue and help urinary
symptoms go back to normal.
This is a multi-center, randomized, sham-controlled, double-blind, dose-finding study in parallel groups of subjects with lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH). All subjects will receive a fixed dose of lemuteporfin injected transurethrally into the prostate followed by transurethral application of either one of three active light doses or a sham light dose. Subjects will be followed for safety and efficacy for a minimum of three months to a maximum of 12 months. The primary study endpoint will be the change from baseline in AUA SI score at three months. ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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