Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults

NCT: NCT06935266 · COMPLETED

NCT IDNCT06935266
StatusCOMPLETED
Start Date2025-04-22
Completion2025-09-27
SponsorTakeda (INDUSTRY)
First posted
Last updated

Brief Summary

The main aim of this study is to check how well healthy adults can tolerate TAK-881 with different dosing schedules. During the study, participants will receive one infusion of TAK-881 under the skin (subcutaneous \[SC\] infusion) on Day 1 at a lower dose level followed by participants receiving multiple infusion of higher dose levels. Participants will be in the study for approximately 19 weeks including screening period and follow-up (End of Treatment \[EOT\]).

Frequently Asked Questions

What is A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults?

A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults is a clinical trial registered under NCT06935266. Current status: COMPLETED.

What is the status of NCT06935266?

The current status of NCT06935266 (A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults) is: COMPLETED.

When did A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults start?

A Study of TAK-881 With and Without Ramp-Up Dosing in Healthy Adults started on 2025-04-22.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.