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NCT05174221 · ClinicalTrials.gov registry record · Phase 1

A Study of Mezagitamab in Adults With Primary Immunoglobulin A Nephropathy Receiving Stable Background Therapy

A Phase 1 study, sponsored by Takeda.

Completed
Registry status
Phase 1
Development phase
17
Enrollment target

NCT05174221: Completed Phase 1 study, sponsored by Takeda.

NCT05174221 is a Phase 1 study that has completed, run by Takeda. The registered enrollment target is 17 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05174221, a Phase 1 study, has completed, sponsored by Takeda.

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target

Study Summary

This study will have two parts. The main aims are to: * check the side effects from mezagitamab. * check for long-term side effects from mezagitamab. Before starting the study, participants will be asked to provide a 24-hour urine sample. A few weeks later, if enrolled they will begin receiving a subcutaneous injection (under the skin) of mezagitamab once a week for 8 weeks then once every 2 weeks for 16 weeks. When treatment has ended, there will be a 24-week follow-up period. Participants who receive benefit from the treatment may continue in the second part of the study where they will be monitored for up to 96 weeks and possibly retreated for another 24 weeks.

Primary Outcome

The severity of TEAEs will be graded using National cancer institute-Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.

Interventions

  • DRUG Mezagitamab

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2022-08-16
Est. Completion 2025-12-15
Phase Phase 1
Takeda

408 total trials

What the finished NCT05174221 record still lists

NCT05174221 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 1 intervention - of which Mezagitamab is the first listed.

NCT05174221 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05174221 about?

NCT05174221 is a clinical study titled "A Study of Mezagitamab in Adults With Primary Immunoglobulin A Nephropathy Receiving Stable Background Therapy". This study will have two parts. The main aims are to: * check the side effects from mezagitamab. * check for long-term side effects from mezagitamab. Before starting the study, participants will be asked to provide a 24-hour urine sample. A few weeks later, if enrolled they will begin receiving a ...

What is the current status of trial NCT05174221?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2022-08-16. Estimated completion is 2025-12-15.

What interventions are being tested in trial NCT05174221?

The interventions under investigation include: Mezagitamab (DRUG).

Who is sponsoring clinical trial NCT05174221?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05174221's enrollment target sits among peer trials

17 1785th of 2000 higher than 215 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05174221, the US trial registry maintained by the National Library of Medicine. NCT05174221 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.