A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants

NCT06953934 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2025-08-08

No results posted yet for this study

Summary

The main objective of this study is to assess the safety and tolerability of ABBV-932 in healthy adult male participants.

Conditions

  • Healthy Volunteer

Interventions

DRUG

ABBV-932

Oral Capsule

Sponsors & Collaborators

Principal Investigators

  • ABBVIE INC. · AbbVie

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-10-14
Primary Completion
2026-02-28
Completion
2026-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06953934 on ClinicalTrials.gov