Clinical Trial

A Study of TAK-881 and HyQvia in Healthy Adults

Completed Phase 1
View on ClinicalTrials.gov →
Summary
The main aim of this study is to understand how the body absorbs, processes, and removes (known as pharmacokinetics or PK) TAK-881 and HyQvia, after they are given as a single injection under the skin in healthy adults. Study participants will receive a single dose of TAK-881 or HyQvia on Day 1. During the study, participants will need to stay at the clinic for 8 days followed by 8 ambulatory follow up visits till Day 85.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2025-03-20; most recent amendment 2026-05-22.
Status change: Recruiting → Completed 2025-08-14
Status change: Not Yet Recruiting → Recruiting 2025-05-06
Trial Details
NCT Number NCT06895967
Lead Sponsor Takeda
Conditions Healthy Volunteers
Enrollment 30 participants
Start Date 2025-03-24
Primary Completion 2025-07-24 (estimated)
Study Completion 2025-08-08 (estimated)
Updated on ClinicalTrials.gov 2026-06-11