Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT07141199

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, Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of ABBV-8736 After Multiple Ascending Doses in Healthy Adult Subjects

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
AbbVie · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
DRUGABBV-8736Intravenous (IV) Infusion
DRUGPlaceboIV Infusion

Timeline

Start date
2025-09-02
Primary completion
2026-03-01
Completion
2026-04-01
First posted
2025-08-26
Last updated
2026-02-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07141199. Inclusion in this directory is not an endorsement.