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NCT04403763 · ClinicalTrials.gov registry record · Phase 1

Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Presbyopia

A Phase 1 study, sponsored by AbbVie.

Terminated
Registry status
Phase 1
Development phase
80
Enrollment target

NCT04403763: Clinical Trial Phase 1 study, sponsored by AbbVie.

NCT04403763 is a Phase 1 study that was terminated before completion, run by AbbVie. The registered enrollment target is 80 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04403763, a Phase 1 study, was terminated before completion, sponsored by AbbVie.

TERMINATED
Registry status
Phase 1
Development phase
80 participants
Enrollment target

Study Summary

The objective of this study is to evaluate the safety, tolerability, pharmacokinetics, and efficacy of AGN-241622 ophthalmic solution for the first time in human participants

Primary Outcome

The number of participants who experience one or more TEAE during the treatment period

Interventions

  • DRUG Vehicle
  • DRUG AGN-241622

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2020-07-27
Est. Completion 2022-12-05
Phase Phase 1
AbbVie

526 total trials

Why NCT04403763 stopped before completion

NCT04403763 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% higher).

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

NCT04403763 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04403763 about?

NCT04403763 is a clinical study titled "Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Presbyopia". The objective of this study is to evaluate the safety, tolerability, pharmacokinetics, and efficacy of AGN-241622 ophthalmic solution for the first time in human participants

What is the current status of trial NCT04403763?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2020-07-27. Estimated completion is 2022-12-05.

What interventions are being tested in trial NCT04403763?

The interventions under investigation include: Vehicle (DRUG), AGN-241622 (DRUG).

Who is sponsoring clinical trial NCT04403763?

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

How this trial's enrollment target compares

Where NCT04403763's enrollment target sits among peer trials

80 672nd of 2000 higher than 1,305 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 NCT04403763, the US trial registry maintained by the National Library of Medicine. NCT04403763 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.