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NCT06849791 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adult Participants

A Phase 1 study of Healthy Volunteer, sponsored by AbbVie.

Active
Registry status
Phase 1
Development phase
9
Enrollment target
1
Study location

NCT06849791: Active Phase 1 study of Healthy Volunteer, sponsored by AbbVie.

NCT06849791 is a Phase 1 study of Healthy Volunteer that is active but no longer recruiting, run by AbbVie. The registered enrollment target is 9 participants, below the 202-participant average among 112 other Healthy Volunteer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06849791, a Phase 1 study of Healthy Volunteer, is active but no longer recruiting, sponsored by AbbVie.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
9 participants
Enrollment target
1
Study location

Study Summary

This study will assess the relative bioavailability and effect of food on pharmacokinetics of ABBV-932 oral administration in healthy adult participants.

Primary Outcome

Cmax of ABBV-932

Conditions Studied

Interventions

  • DRUG ABBV-932

Study Locations (1)

Illinois

  • Acpru /Id# 266649 - Grayslake

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2025-02-26
Est. Completion 2026-03
Phase Phase 1
AbbVie

526 total trials

What the registry record for NCT06849791 still lists

NCT06849791 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 202-participant average among 112 other Healthy Volunteer trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Healthy Volunteer appearing as the primary indexed condition, and to 1 intervention - of which ABBV-932 is the first listed.

NCT06849791 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06849791 about?

NCT06849791 is a clinical study titled "A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adult Participants". This study will assess the relative bioavailability and effect of food on pharmacokinetics of ABBV-932 oral administration in healthy adult participants.

What is the current status of trial NCT06849791?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 9 participants. The study started on 2025-02-26. Estimated completion is 2026-03.

What conditions does trial NCT06849791 study?

This clinical trial studies the following conditions: Healthy Volunteer.

What interventions are being tested in trial NCT06849791?

The interventions under investigation include: ABBV-932 (DRUG).

Who is sponsoring clinical trial NCT06849791?

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

Where is trial NCT06849791 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Volunteer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06849791's enrollment target sits among peer trials

9 109th of 112 higher than 4 of 112 other Healthy Volunteer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Volunteer 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 NCT06849791, the US trial registry maintained by the National Library of Medicine. NCT06849791 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.