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NCT04060173 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ABP-671

A Phase 1 study, sponsored by Atom Therapeutics Co..

Completed
Registry status
Phase 1
Development phase
27
Enrollment target

NCT04060173: Completed Phase 1 study, sponsored by Atom Therapeutics Co..

NCT04060173 is a Phase 1 study that has completed, run by Atom Therapeutics Co.. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04060173, a Phase 1 study, has completed, sponsored by Atom Therapeutics Co..

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending doses of ABP-671 administered orally in subjects with hyperuricemia.

Primary Outcome

Measured by the number of patients with AEs

Interventions

  • OTHER Placebo
  • DRUG ABP-671

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2019-09-05
Est. Completion 2020-02-07
Phase Phase 1
Atom Therapeutics Co.

9 total trials

What the finished NCT04060173 record still lists

NCT04060173 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

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

NCT04060173 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04060173 about?

NCT04060173 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ABP-671". The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending doses of ABP-671 administered orally in subjects with hyperuricemia.

What is the current status of trial NCT04060173?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2019-09-05. Estimated completion is 2020-02-07.

What interventions are being tested in trial NCT04060173?

The interventions under investigation include: Placebo (OTHER), ABP-671 (DRUG).

Who is sponsoring clinical trial NCT04060173?

This trial is sponsored by Atom Therapeutics Co., which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04060173's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 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 NCT04060173, the US trial registry maintained by the National Library of Medicine. NCT04060173 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.