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Completed Phase 2 Interventional

A Placebo Controlled Study of MR901 (Talaporfin Sodium Sodium + a Drug-activating Device) for the Relief of Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia

ClinicalTrials.gov ID: NCT02326454

Public ClinicalTrials.gov record NCT02326454. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 5:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Randomised, Double-blind, Placebo Controlled, Study of MR901 in Patients With Moderate to Severe Lower Urinary Tract Symptoms (LUTS) Due to Benign Prostatic Hyperplasia (BPH)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study investigates the safety and efficacy of a photosensitive drug (talaporfin sodium) activated by an intraurethrally placed drug-activating device. MR901 is a code used to identify the combination of talaporfin sodium and the drug-activating device. Two different light doses will be tested against placebo groups in this 4-arm study.

Study identification

NCT ID
NCT02326454
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Light Sciences Oncology
Industry
Enrollment
225 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2014 (Type not available)
Primary completion
Mar 29, 2017 (Actual)
Completion
Mar 29, 2017 (Actual)
Last update posted
Aug 8, 2018

2014 – 2017

United States locations

U.S. sites
41
U.S. states
22
U.S. cities
40
Facility City State ZIP Site status
Not listed Anniston Alabama 36207 —
Not listed Huntsville Alabama 35801 —
Not listed Anchorage Alaska 99503 —
Not listed Laguna Hills California 92653 —
Not listed Los Angeles California 90017 —
Not listed Murrieta California 92562 —
Not listed San Diego California 92120 —
Not listed Tarzana California 91356 —
Not listed Denver Colorado 80220 —
Not listed Aventura Florida 33180 —
Not listed Bradenton Florida 34205 —
Not listed Coral Gables Florida 33146 —
Not listed Pompano Beach Florida 33060 —
Not listed St. Petersburg Florida 33710 —
Not listed Tampa Florida 33607 —
Not listed Bloomington Indiana 47403 —
Not listed Greenwood Indiana 46143 —
Not listed New Orleans Louisiana 70006 —
Not listed New Orleans Louisiana 70115 —
Not listed Greenbelt Maryland 20770 —
Not listed Towson Maryland 21204 —
Not listed Chestnut Hill Massachusetts 02467 —
Not listed Las Vegas Nevada 89144 —
Not listed Edison New Jersey 08837 —
Not listed Albuquerque New Mexico 87109 —
Not listed Garden City New York 11530 —
Not listed New York New York 10016 —
Not listed Newburgh New York 12601 —
Not listed Poughkeepsie New York 12601 —
Not listed Concord North Carolina 28025 —
Not listed Cincinnati Ohio 45212 —
Not listed Middleburg Heights Ohio 44130 —
Not listed Springfield Oregon 97477 —
Not listed Bala-Cynwyd Pennsylvania 19004 —
Not listed Bryn Mawr Pennsylvania 19010 —
Not listed Myrtle Beach South Carolina 29572 —
Not listed Knoxville Tennessee 37923 —
Not listed Dallas Texas 75231 —
Not listed Houston Texas 77094 —
Not listed Salt Lake City Utah 84124 —
Not listed Mountlake Terrace Washington 98043 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02326454, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 8, 2018 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02326454 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →