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NCT02766621 · ClinicalTrials.gov registry record · Phase 1

Evaluation Of Safety, Tolerability And Pharmacokinetics Of Single And Multiple Doses Of Compound PF-06823859

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
62
Enrollment target

NCT02766621: Completed Phase 1 study, sponsored by Pfizer.

NCT02766621 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 62 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

NCT02766621, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
62 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety, tolerability and pharmacokinetics of escalating single and multiple intravenous (IV) infusions and subcutaneous (SC) injections of PF 06823859 in healthy subjects.

Primary Outcome

Safety

Interventions

  • BIOLOGICAL PF-06823859
  • DRUG Placebo injection SC/IV

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2016-05-27
Est. Completion 2017-09-26
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT02766621 record still lists

NCT02766621 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 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 2 interventions - of which PF-06823859 is the first listed.

NCT02766621 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02766621 about?

NCT02766621 is a clinical study titled "Evaluation Of Safety, Tolerability And Pharmacokinetics Of Single And Multiple Doses Of Compound PF-06823859". The purpose of this study is to determine the safety, tolerability and pharmacokinetics of escalating single and multiple intravenous (IV) infusions and subcutaneous (SC) injections of PF 06823859 in healthy subjects.

What is the current status of trial NCT02766621?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 62 participants. The study started on 2016-05-27. Estimated completion is 2017-09-26.

What interventions are being tested in trial NCT02766621?

The interventions under investigation include: PF-06823859 (BIOLOGICAL), Placebo injection SC/IV (DRUG).

Who is sponsoring clinical trial NCT02766621?

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 NCT02766621's enrollment target sits among peer trials

62 824th of 2000 higher than 1,173 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 NCT02766621, the US trial registry maintained by the National Library of Medicine. NCT02766621 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.