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NCT03922607 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 in Healthy Volunteers and in Participants With Chronic Plaque Psoriasis

A Phase 1 study, sponsored by AbbVie.

Completed
Registry status
Phase 1
Development phase
65
Enrollment target

NCT03922607: Completed Phase 1 study, sponsored by AbbVie.

NCT03922607 is a Phase 1 study that has completed, run by AbbVie. The registered enrollment target is 65 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

NCT03922607, a Phase 1 study, has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 1
Development phase
65 participants
Enrollment target

Study Summary

This is a study to evaluate pharmacokinetics (PK), safety and tolerability of ABBV-157 in healthy volunteers and in participants with chronic plaque psoriasis, and to evaluate the efficacy of ABBV-157 in the participants with psoriasis. This study consists of two substudies. Substudy 1 is a randomized, double-blind, placebo-controlled evaluation of multiple ascending oral doses of ABBV-157 in healthy adult volunteers. Substudy 2 is a randomized, double-blind, placebo-controlled study in which participants with moderate to severe chronic plaque psoriasis will be administered multiple oral doses of ABBV-157.

Primary Outcome

Maximum observed plasma concentration (Cmax) of ABBV-157

Interventions

  • DRUG ABBV-157
  • DRUG Placebo for ABBV-157

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2019-06-11
Est. Completion 2021-04-13
Phase Phase 1
AbbVie

526 total trials

What the finished NCT03922607 record still lists

NCT03922607 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 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 ABBV-157 is the first listed.

NCT03922607 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03922607 about?

NCT03922607 is a clinical study titled "A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 in Healthy Volunteers and in Participants With Chronic Plaque Psoriasis". This is a study to evaluate pharmacokinetics (PK), safety and tolerability of ABBV-157 in healthy volunteers and in participants with chronic plaque psoriasis, and to evaluate the efficacy of ABBV-157 in the participants with psoriasis. This study consists of two substudies. Substudy 1 is a randomiz...

What is the current status of trial NCT03922607?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 65 participants. The study started on 2019-06-11. Estimated completion is 2021-04-13.

What interventions are being tested in trial NCT03922607?

The interventions under investigation include: ABBV-157 (DRUG), Placebo for ABBV-157 (DRUG).

Who is sponsoring clinical trial NCT03922607?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03922607's enrollment target sits among peer trials

65 798th of 2000 higher than 1,193 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 NCT03922607, the US trial registry maintained by the National Library of Medicine. NCT03922607 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.