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NCT00603187 · ClinicalTrials.gov registry record · Phase 1

ACY-7 Oral Administration of Acyline

A Phase 1 study, sponsored by University of Washington.

Completed
Registry status
Phase 1
Development phase
4
Enrollment target

NCT00603187: Completed Phase 1 study, sponsored by University of Washington.

NCT00603187 is a Phase 1 study that has completed, run by University of Washington. The registered enrollment target is 4 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00603187, a Phase 1 study, has completed, sponsored by University of Washington.

COMPLETED
Registry status
Phase 1
Development phase
4 participants
Enrollment target

Study Summary

We propose oral dosing of gastrointestinal permeation enhancement technology \[GIPET\] enhanced oral acyline at 20 mg everyday for one week to determine the steady-state (multiple-dose) pharmacokinetics of oral acyline in four normal, healthy young men.

Primary Outcome

Blood for measurement of serum testosterone was obtained prior to the 1st, 5th and 6th dose of GIPET™-enhanced oral acyline and 0.5,1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48 and 60 hours after the 7th dose.

Interventions

  • DRUG Acyline

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2008-01
Est. Completion 2008-02
Phase Phase 1
University of Washington

1,048 total trials

What the finished NCT00603187 record still lists

NCT00603187 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which Acyline is the first listed.

NCT00603187 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00603187 about?

NCT00603187 is a clinical study titled "ACY-7 Oral Administration of Acyline". We propose oral dosing of gastrointestinal permeation enhancement technology \[GIPET\] enhanced oral acyline at 20 mg everyday for one week to determine the steady-state (multiple-dose) pharmacokinetics of oral acyline in four normal, healthy young men.

What is the current status of trial NCT00603187?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2008-01. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00603187?

The interventions under investigation include: Acyline (DRUG).

Who is sponsoring clinical trial NCT00603187?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00603187's enrollment target sits among peer trials

4 1995th of 2000 higher than 2 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00603187, the US trial registry maintained by the National Library of Medicine. NCT00603187 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.