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NCT02189304 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics and Safety Study of PT010 in Healthy Subjects

A Phase 1 study, sponsored by Pearl Therapeutics.

Completed
Registry status
Phase 1
Development phase
59
Enrollment target

NCT02189304: Completed Phase 1 study, sponsored by Pearl Therapeutics.

NCT02189304 is a Phase 1 study that has completed, run by Pearl Therapeutics. The registered enrollment target is 59 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02189304, a Phase 1 study, has completed, sponsored by Pearl Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
59 participants
Enrollment target

Study Summary

This is a single-center, Phase I, healthy adult subject study with a randomized, double blind, three period, three-treatment, cross-over design.

Primary Outcome

The safety of PT010 and PT009 and Symbicort Turbohaler will be assessed based on physical examination, adverse events, vital signs, clinical laboratory values, and electrocardiogram

Interventions

  • DRUG PT010
  • DRUG PT009
  • DRUG Symbicort Turbohaler

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2014-06-01
Est. Completion 2014-09-01
Phase Phase 1
Pearl Therapeutics

31 total trials

What the finished NCT02189304 record still lists

NCT02189304 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 3 interventions - of which PT010 is the first listed.

NCT02189304 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02189304 about?

NCT02189304 is a clinical study titled "Pharmacokinetics and Safety Study of PT010 in Healthy Subjects". This is a single-center, Phase I, healthy adult subject study with a randomized, double blind, three period, three-treatment, cross-over design.

What is the current status of trial NCT02189304?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 59 participants. The study started on 2014-06-01. Estimated completion is 2014-09-01.

What interventions are being tested in trial NCT02189304?

The interventions under investigation include: PT010 (DRUG), PT009 (DRUG), Symbicort Turbohaler (DRUG).

Who is sponsoring clinical trial NCT02189304?

This trial is sponsored by Pearl Therapeutics, which has 31 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02189304's enrollment target sits among peer trials

59 895th of 2000 higher than 1,106 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 NCT02189304, the US trial registry maintained by the National Library of Medicine. NCT02189304 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.