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New prostate drug delivered directly to target

NCT ID NCT07264205

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This early study tests a new treatment called RT-310 for men with enlarged prostate (BPH) who have bothersome urinary symptoms. RT-310 is a drug delivered directly into the prostate to reduce side effects. The study will check if it is safe and feasible in 20 men aged 50 to 80.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
RT-310 (a drug delivered directly to the prostate)
What this could lead to
If it works, this could lead to a new treatment for BPH that reduces side effects by targeting the prostate directly.
What could go wrong
This is a very early, small study (20 men) focused only on safety and feasibility. It may not show clear benefit, and the approach might not work in larger trials.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2025

Expected to finish

Jun 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

50 to 80 years

Sex

Male participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male gender * Diagnosis of symptomatic BPH * Age ≥ 50 years up to 80 years * International Prostate Symptom Score (IPSS) ≥ 13 * Peak urine flow rate ≥ 5mL/sec and ≤ 12 ml/sec, voided volume ≥ 100 ml * Prostate volume 30 to 80 cc per ultrasound * Post void residual (PVR) urine ≤ 250 ml * Inadequate response and/or refusal of medical therapy for LUTS Exclusion Criteria: * Unable or unwilling to sign the informed consent form (ICF) and/or comply with the study follow-up requirements * Current urinary retention requiring catheterization * Unwilling to abstain from unprotected sexual intercourse for 3 months * Unwilling to abstain from any child conceiving activities for 6 months * Have an obstructive or protruding median lobe of the prostate * High bladder neck determined by Investigator * Active urinary tract infection at time of treatment * Previous BPH surgical procedure or implants, urethral stricture, Any prior minimally invasive intervention (e.g. TUNA, Balloon, Microwave, Rezūm, UroLift) or surgical intervention of the prostate * Previous pelvic surgery or irradiation * History of neurogenic or atonic bladder * Stress urinary incontinence, mixed or urge incontinence * Biopsy of the prostate within the past 6 weeks * Life expectancy estimated to be less than 1 year * History of prostate or bladder cancer, confirmed or suspected malignancy of prostate or bladder * History of compromised renal function or upper urinary tract disease * Known coagulopathies or participant on anticoagulants or antiplatelets other than aspirin ≤ 100 mg (unless antiplatelets are withheld minimum 3 days prior to procedure) * Use of the following medications pre-screening: Within 6 months of baseline assessment, unless documented on stable dose for ≥ 12 months: 5-alpha-reductase inhibitors (e.g. dutasteride, Avodart, finasteride, Proscar, Propecia) Within 4 months of baseline assessment: estrogen, any drug producing androgen suppression, or anabolic steroids Within 2 weeks of baseline assessment: alpha-blockers, gonadotropin- releasing hormonal analogs, anticholinergics or cholinergic medication or phenylephrine, pseudoephedrine, diphenhydramine or imipramine medications Within 1 week of baseline assessment, unless documented on stable dose for ≥ 6 months: beta blockers, antidepressants, anticonvulsants, and antispasmodics * Cystolithiasis within the prior 3 months * History of co-morbidities that would affect having an elective urological procedure including prostatitis, conditions that preclude the RT-310. * Other co-morbidities that could impact the study results such as: Severe cardiac arrhythmias uncontrolled by medications or pacemaker Congestive heart failure New York Heart Association (NYHA) III or IV History of uncontrolled diabetes mellitus Significant respiratory disease in which hospitalization may be required * Known immunosuppression (i.e. AIDS, post-transplant, undergoing chemotherapy) * Currently enrolled in any other investigational clinical research trial that has not completed the primary endpoint. * No more than two documented active urinary tract infections (UTI) by culture or bacterial prostatitis within last year documented by culture (UTI is defined as \>100,000 colonies per ml urine from midstream clean catch or catheterization specimen) * Current gross hematuria and/or visible hematuria with participant urine sample without known contributing factor * Presence of a penile implant or stent(s) in the urethra or prostate * PSA \> 10 ng/ml unless prostate cancer is ruled out by biopsy. If PSA is \> 4 ng/ml and ≤ 10 ng/ml, prostate cancer must be ruled out to the satisfaction of the investigator via additional tests including digital rectal exam (DRE) and/or biopsy * Active or history of epididymitis within the past 3 months * Sensitivity to RT-310 * Parkinson's disease or other neurologic disease that may impact bladder function such as stroke, TIA, multiple sclerosis * Active infection including prostatitis

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Research Site

    Santo Domingo, Dominican Republic

More trials for these conditions

Other studies related to the condition(s) this trial covers.