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NCT00759135 · ClinicalTrials.gov registry record · Phase 2

Phase 2 Study of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) (Enlarged Prostate)

A Phase 2 study, sponsored by Nymox Corporation.

Completed
Registry status
Phase 2
Development phase
85
Enrollment target

NCT00759135: Completed Phase 2 study, sponsored by Nymox Corporation.

NCT00759135 is a Phase 2 study that has completed, run by Nymox Corporation. The registered enrollment target is 85 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (36% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00759135, a Phase 2 study, has completed, sponsored by Nymox Corporation.

COMPLETED
Registry status
Phase 2
Development phase
85 participants
Enrollment target

Study Summary

This completed study evaluated the safety and efficacy of two dose levels of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) versus finasteride.

Interventions

  • DRUG 2.5 mg NX-1207
  • DRUG 0.125 mg NX-1207
  • DRUG finasteride

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2007-05
Est. Completion 2008-05
Phase Phase 2
Nymox Corporation

6 total trials

What the finished NCT00759135 record still lists

NCT00759135 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 85 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (36% lower).

The record links to 0 conditions, and to 3 interventions - of which 2.5 mg NX-1207 is the first listed.

NCT00759135 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00759135 about?

NCT00759135 is a clinical study titled "Phase 2 Study of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) (Enlarged Prostate)". This completed study evaluated the safety and efficacy of two dose levels of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) versus finasteride.

What is the current status of trial NCT00759135?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 85 participants. The study started on 2007-05. Estimated completion is 2008-05.

What interventions are being tested in trial NCT00759135?

The interventions under investigation include: 2.5 mg NX-1207 (DRUG), 0.125 mg NX-1207 (DRUG), finasteride (DRUG).

Who is sponsoring clinical trial NCT00759135?

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 NCT00759135's enrollment target sits among peer trials

85 820th of 2000 higher than 1,179 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT00759135, the US trial registry maintained by the National Library of Medicine. NCT00759135 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.