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NCT01369836 · ClinicalTrials.gov registry record · Phase 1

Study Of Single Doses Of PF-06291826 (Tafamidis) In Japanese And Western Subjects

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
21
Enrollment target

NCT01369836: Completed Phase 1 study, sponsored by Pfizer.

NCT01369836 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 21 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01369836, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

The purpose of this study is the following: * To evaluate the safety, tolerability, and pharmacokinetics (PK) of orally administered tafamidis in Japanese and Western healthy volunteers at single dose. * To compare Japanese and Western PK profiles. * Determine the PD stabilization effect of tafamidis on human transthyretin (TTR) in a validated ex vivo assay.

Interventions

  • DRUG Placebo
  • DRUG Tafamidis meglumin

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2011-07
Est. Completion 2011-08
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT01369836 record still lists

NCT01369836 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower).

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

NCT01369836 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01369836 about?

NCT01369836 is a clinical study titled "Study Of Single Doses Of PF-06291826 (Tafamidis) In Japanese And Western Subjects". The purpose of this study is the following: * To evaluate the safety, tolerability, and pharmacokinetics (PK) of orally administered tafamidis in Japanese and Western healthy volunteers at single dose. * To compare Japanese and Western PK profiles. * Determine the PD stabilization effect of tafamid...

What is the current status of trial NCT01369836?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2011-07. Estimated completion is 2011-08.

What interventions are being tested in trial NCT01369836?

The interventions under investigation include: Placebo (DRUG), Tafamidis meglumin (DRUG).

Who is sponsoring clinical trial NCT01369836?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01369836's enrollment target sits among peer trials

21 1615th of 2000 higher than 372 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 NCT01369836, the US trial registry maintained by the National Library of Medicine. NCT01369836 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.