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NCT01305824 · ClinicalTrials.gov registry record · Phase 2

A Study of PRT-201 Administered Immediately After Arteriovenous Fistula Creation in Patients With Chronic Kidney Disease

A Phase 2 study, sponsored by Proteon Therapeutics.

Completed
Registry status
Phase 2
Development phase
151
Enrollment target

NCT01305824: Completed Phase 2 study, sponsored by Proteon Therapeutics.

NCT01305824 is a Phase 2 study that has completed, run by Proteon Therapeutics. The registered enrollment target is 151 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01305824, a Phase 2 study, has completed, sponsored by Proteon Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
151 participants
Enrollment target

Study Summary

The purpose of this study is to determine if PRT-201 when applied to a limited segment of your blood vessel (about 2 inches) immediately after surgery to create an arteriovenous fistula is safe and improves the patency of your fistula. PRT-201 is a protein that has been shown to help keep vessels open ("patent") when applied to the outside surface of the blood vessels (arteries and veins) in AVF patients in a previous study.

Interventions

  • DRUG Placebo
  • DRUG PRT-201

Trial Details

FieldValue
Enrollment Target 151 participants
Start Date 2011-03
Est. Completion 2012-11
Phase Phase 2
Proteon Therapeutics

7 total trials

What the finished NCT01305824 record still lists

NCT01305824 is an interventional study that assigns participants to a tested intervention. The registered 151 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% higher).

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

NCT01305824 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01305824 about?

NCT01305824 is a clinical study titled "A Study of PRT-201 Administered Immediately After Arteriovenous Fistula Creation in Patients With Chronic Kidney Disease". The purpose of this study is to determine if PRT-201 when applied to a limited segment of your blood vessel (about 2 inches) immediately after surgery to create an arteriovenous fistula is safe and improves the patency of your fistula. PRT-201 is a protein that has been shown to help keep vessels op...

What is the current status of trial NCT01305824?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 151 participants. The study started on 2011-03. Estimated completion is 2012-11.

What interventions are being tested in trial NCT01305824?

The interventions under investigation include: Placebo (DRUG), PRT-201 (DRUG).

Who is sponsoring clinical trial NCT01305824?

This trial is sponsored by Proteon Therapeutics, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01305824's enrollment target sits among peer trials

151 454th of 2000 higher than 1,546 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 NCT01305824, the US trial registry maintained by the National Library of Medicine. NCT01305824 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.