Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00945490 · ClinicalTrials.gov registry record · Phase 3

Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018

A Phase 3 study, sponsored by Nymox Corporation.

Completed
Registry status
Phase 3
Development phase
500
Enrollment target

NCT00945490: Completed Phase 3 study, sponsored by Nymox Corporation.

NCT00945490 is a Phase 3 study that has completed, run by Nymox Corporation. The registered enrollment target is 500 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00945490, a Phase 3 study, has completed, sponsored by Nymox Corporation.

COMPLETED
Registry status
Phase 3
Development phase
500 participants
Enrollment target

Study Summary

This study will evaluate the safety and efficacy of a 2.5 mg dose of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) as compared to placebo.

Interventions

  • DRUG Placebo
  • DRUG NX-1207

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2009-05
Est. Completion 2014-05
Phase Phase 3
Nymox Corporation

6 total trials

What the finished NCT00945490 record still lists

NCT00945490 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (35% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00945490 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00945490 about?

NCT00945490 is a clinical study titled "Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) NX02-0018". This study will evaluate the safety and efficacy of a 2.5 mg dose of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) as compared to placebo.

What is the current status of trial NCT00945490?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 500 participants. The study started on 2009-05. Estimated completion is 2014-05.

What interventions are being tested in trial NCT00945490?

The interventions under investigation include: Placebo (DRUG), NX-1207 (DRUG).

Who is sponsoring clinical trial NCT00945490?

This trial is sponsored by Nymox Corporation, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00945490's enrollment target sits among peer trials

500 744th of 2000 higher than 1,226 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00001230 · 500 participants

    Host Response to Infection and Treatment in Filarial Diseases

  • NCT00001529 · 500 participants

    Improved Methods of Cell Selection for Bone Marrow Transplant Alternatives

  • NCT00697411 · 500 participants

    Study of Selected X-Linked Disorders: Aicardi Syndrome

  • NCT00903110 · 500 participants

    Global Patient Registry to Monitor Long-term Safety and Effectiveness of Increlex® in Children and Adolescents With Severe Primary Insulin-like Growth Factor-1 Deficiency (SPIGFD).

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00945490, the US trial registry maintained by the National Library of Medicine. NCT00945490 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.