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NCT06009237 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Healthy Japanese and Han Chinese Participants

A Phase 1 study, sponsored by AbbVie.

Terminated
Registry status
Phase 1
Development phase
24
Enrollment target

NCT06009237: Clinical Trial Phase 1 study, sponsored by AbbVie.

NCT06009237 is a Phase 1 study that was terminated before completion, run by AbbVie. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06009237, a Phase 1 study, was terminated before completion, sponsored by AbbVie.

TERMINATED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

The objective of this study is to assess the pharmacokinetics (PK), safety, and tolerability of ABBV-903 or placebo in healthy adult Japanese and Han Chinese subjects.

Primary Outcome

Cmax of ABBV-903 will be assessed.

Interventions

  • DRUG ABBV-903
  • DRUG Placebo for ABBV-903

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2023-08-23
Est. Completion 2023-10-30
Phase Phase 1
AbbVie

526 total trials

Why NCT06009237 stopped before completion

NCT06009237 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 2 interventions - of which ABBV-903 is the first listed.

NCT06009237 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06009237 about?

NCT06009237 is a clinical study titled "A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Healthy Japanese and Han Chinese Participants". The objective of this study is to assess the pharmacokinetics (PK), safety, and tolerability of ABBV-903 or placebo in healthy adult Japanese and Han Chinese subjects.

What is the current status of trial NCT06009237?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2023-08-23. Estimated completion is 2023-10-30.

What interventions are being tested in trial NCT06009237?

The interventions under investigation include: ABBV-903 (DRUG), Placebo for ABBV-903 (DRUG).

Who is sponsoring clinical trial NCT06009237?

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

How this trial's enrollment target compares

Where NCT06009237's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 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 NCT06009237, the US trial registry maintained by the National Library of Medicine. NCT06009237 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.