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NCT00791388 · ClinicalTrials.gov registry record · Phase 1

Multiple Rising Oral Dose Study of PG 760564 Administered Twice Daily to Healthy Male/Female Volunteers for 14 Days

A Phase 1 study, sponsored by Procter and Gamble.

Completed
Registry status
Phase 1
Development phase
45
Enrollment target

NCT00791388: Completed Phase 1 study, sponsored by Procter and Gamble.

NCT00791388 is a Phase 1 study that has completed, run by Procter and Gamble. The registered enrollment target is 45 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00791388, a Phase 1 study, has completed, sponsored by Procter and Gamble.

COMPLETED
Registry status
Phase 1
Development phase
45 participants
Enrollment target

Study Summary

This study is a multiple ascending dose study to Assess the Safety, Tolerability, and Pharmacokinetics of orally dosed PG 760564 Administered Twice Daily to Healthy Male and Female Volunteers for 14 Days (27 Doses).

Primary Outcome

the area under the plasma concentration-time curve over a dosing interval (τ = 12 hours) on Day 14 of Multiple Dose Oral Administration of PG-760564 Given Every 12 Hours

Interventions

  • DRUG Placebo
  • DRUG PG-760564

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2005-08
Est. Completion 2006-01
Phase Phase 1
Procter and Gamble

70 total trials

What the finished NCT00791388 record still lists

NCT00791388 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% lower).

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

NCT00791388 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00791388 about?

NCT00791388 is a clinical study titled "Multiple Rising Oral Dose Study of PG 760564 Administered Twice Daily to Healthy Male/Female Volunteers for 14 Days". This study is a multiple ascending dose study to Assess the Safety, Tolerability, and Pharmacokinetics of orally dosed PG 760564 Administered Twice Daily to Healthy Male and Female Volunteers for 14 Days (27 Doses).

What is the current status of trial NCT00791388?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 45 participants. The study started on 2005-08. Estimated completion is 2006-01.

What interventions are being tested in trial NCT00791388?

The interventions under investigation include: Placebo (DRUG), PG-760564 (DRUG).

Who is sponsoring clinical trial NCT00791388?

This trial is sponsored by Procter and Gamble, which has 70 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00791388's enrollment target sits among peer trials

45 1066th of 2000 higher than 915 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 NCT00791388, the US trial registry maintained by the National Library of Medicine. NCT00791388 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.