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NCT07141199 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug Moves Through the Body of Intravenous Infusions of ABBV-8736 in Adult Healthy Volunteers

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

Active
Registry status
Phase 1
Development phase
24
Enrollment target
1
Study location

NCT07141199 is a Phase 1 study of Healthy Volunteer that is active but no longer recruiting, run by AbbVie. The registered enrollment target is 24 participants, below the 202-participant average among 112 other Healthy Volunteer trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07141199, 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
24 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to assess the safety, tolerability, pharmacokinetics, and immunogenicity following multiple intravenous (IV) ascending doses of ABBV-8736 in healthy adult participants.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG ABBV-8736

Study Locations (1)

Illinois

  • Acpru /Id# 277377 - Grayslake

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2025-09-02
Est. Completion 2026-04
Phase Phase 1

Sponsor

AbbVie

526 total trials

What the Registry Record Tells You About NCT07141199

The ClinicalTrials.gov registry entry for NCT07141199 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 202-participant average among 112 other Healthy Volunteer trials with a reported enrollment target (88% lower). The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Volunteer appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07141199 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT07141199 about?

NCT07141199 is a clinical study titled "A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug Moves Through the Body of Intravenous Infusions of ABBV-8736 in Adult Healthy Volunteers". The objective of this study is to assess the safety, tolerability, pharmacokinetics, and immunogenicity following multiple intravenous (IV) ascending doses of ABBV-8736 in healthy adult participants.

What is the current status of trial NCT07141199?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2025-09-02. Estimated completion is 2026-04.

What conditions does trial NCT07141199 study?

This clinical trial studies the following conditions: Healthy Volunteer.

What interventions are being tested in trial NCT07141199?

The interventions under investigation include: Placebo (DRUG), ABBV-8736 (DRUG).

Who is sponsoring clinical trial NCT07141199?

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

Where is trial NCT07141199 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.