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NCT03210961 · ClinicalTrials.gov registry record · Phase 1

A First in Human Study to Evaluate Safety, Tolerability, and Pharmacology of PF-06826647 in Healthy Subjects and Subjects With Plaque Psoriasis

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
109
Enrollment target

NCT03210961: Completed Phase 1 study, sponsored by Pfizer.

NCT03210961 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 109 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03210961, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
109 participants
Enrollment target

Study Summary

This first in human study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-06826647 in healthy subjects and subjects with plaque psoriasis.

Primary Outcome

Maximum absolute values and changes from baseline for vital signs (for supine systolic/diastolic blood pressure \[BP\] and supine pulse rate \[PR\]) were summarized descriptively by treatment. Numbers of participants meeting the categorical criteria were provided. Number of participants in PBO SAD cohorts = number of participants in \[PBO SAD (3mg, 10mg)\] cohorts + number of participants in \[PBO SAD -\> PBO QD MAD\] cohorts.

Interventions

  • OTHER Placebo tablet
  • DRUG PF-06826647 tablet
  • DRUG PF-06826647 oral suspension
  • OTHER Placebo oral solution/suspension

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2017-07-14
Est. Completion 2019-01-25
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT03210961 record still lists

NCT03210961 is an interventional study that assigns participants to a tested intervention. The registered 109 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% higher).

The record links to 0 conditions, and to 4 interventions - of which Placebo tablet is the first listed.

NCT03210961 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03210961 about?

NCT03210961 is a clinical study titled "A First in Human Study to Evaluate Safety, Tolerability, and Pharmacology of PF-06826647 in Healthy Subjects and Subjects With Plaque Psoriasis". This first in human study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-06826647 in healthy subjects and subjects with plaque psoriasis.

What is the current status of trial NCT03210961?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 109 participants. The study started on 2017-07-14. Estimated completion is 2019-01-25.

What interventions are being tested in trial NCT03210961?

The interventions under investigation include: Placebo tablet (OTHER), PF-06826647 tablet (DRUG), PF-06826647 oral suspension (DRUG), Placebo oral solution/suspension (OTHER).

Who is sponsoring clinical trial NCT03210961?

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 NCT03210961's enrollment target sits among peer trials

109 522nd of 2000 higher than 1,478 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 NCT03210961, the US trial registry maintained by the National Library of Medicine. NCT03210961 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.