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NCT06980480 · ClinicalTrials.gov registry record · Phase 3

A Study of Gammagard Liquid (Immune Globulin Infusion, 10%) to Prevent Infections in Adults With Multiple Myeloma

A Phase 3 study of Multiple Myeloma and Secondary Immunodeficiency, sponsored by Takeda.

Recruiting
Registry status
Phase 3
Development phase
183
Enrollment target
16
Study locations

NCT06980480: Recruiting Phase 3 study of Multiple Myeloma and Secondary Immunodeficiency, sponsored by Takeda.

NCT06980480 is a Phase 3 study of Multiple Myeloma and Secondary Immunodeficiency that is actively recruiting participants, run by Takeda. The registered enrollment target is 183 participants, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (66% lower). The trial reports 16 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06980480, a Phase 3 study of Multiple Myeloma and Secondary Immunodeficiency, is actively recruiting participants, sponsored by Takeda.

RECRUITING
Registry status
Phase 3
Development phase
183 participants
Enrollment target
16
Study locations

Study Summary

Multiple myeloma is a cancer of the plasma cells in the bone marrow. The main aim of this study is to learn how well the Immune Globulin Infusion (human), 10 percentage (%) (IGI, 10%) can help prevent infections in participants with multiple myeloma receiving B-cell maturation antigen (BCMA) x cluster of differentiation 3 (CD3) directed bispecific antibody therapy. Participants will be randomly assigned to one of two groups: 1. Primary infection prevention group: They will receive IGI, 10% for 12 months. 2. Secondary infection prevention group: They will only receive IGI, 10% if they develop a serious infection during the 12 months study period. During the study, participants will visit their study clinic 15 times (for 4-week dosing interval) or 19 times (for 3-week dosing interval) and their total participation duration will be up to 14 months (including screening period of up to 8 weeks).

Interventions

  • BIOLOGICAL IGI, 10%

Study Locations (16)

Other

  • Universitaetsklinikum St. Poelten - Sankt Pölten
  • Krankenhaus der Barmherzigen Schwestern Wien - Vienna
  • St. Antonius Ziekenhuis - Nieuwegein
  • Aidport sp. z o.o. - Skorzewo
  • County Hospital (Stafford Hospital) - Stafford

Alabama

  • Infirmary Health - Diagnostic & Medical Clinic (DMC) - Mobile

California

  • Chao Family Comprehensive Cancer Center UCI - Orange

Kansas

  • University of Kansas - Westwood

Maryland

  • University of Maryland | Greenebaum Cancer Center - Baltimore

Michigan

  • Henry Ford Health System - Detroit

Missouri

  • Washington University School of Medicine - St Louis

New York

  • New York Oncology Hematology - Albany

Trial Details

FieldValue
Enrollment Target 183 participants
Start Date 2026-01-14
Est. Completion 2028-09-11
Phase Phase 3
Takeda

408 total trials

What NCT06980480 shows while recruiting

NCT06980480 is an interventional study that assigns participants to a tested intervention. The registered 183 participants enrollment target is mid-sized for trials with a published cap, below the 546-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (66% lower).

The record links to 2 conditions, with Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention - of which IGI, 10% is the first listed.

NCT06980480 lists 16 locations in 12 states (Other, Alabama, California).

Frequently Asked Questions

What is clinical trial NCT06980480 about?

NCT06980480 is a clinical study titled "A Study of Gammagard Liquid (Immune Globulin Infusion, 10%) to Prevent Infections in Adults With Multiple Myeloma". Multiple myeloma is a cancer of the plasma cells in the bone marrow. The main aim of this study is to learn how well the Immune Globulin Infusion (human), 10 percentage (%) (IGI, 10%) can help prevent infections in participants with multiple myeloma receiving B-cell maturation antigen (BCMA) x clus...

What is the current status of trial NCT06980480?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 183 participants. The study started on 2026-01-14. Estimated completion is 2028-09-11.

What conditions does trial NCT06980480 study?

This clinical trial studies the following conditions: Multiple Myeloma, Secondary Immunodeficiency.

What interventions are being tested in trial NCT06980480?

The interventions under investigation include: IGI, 10% (BIOLOGICAL).

Who is sponsoring clinical trial NCT06980480?

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

Where is trial NCT06980480 being conducted?

This trial has 16 study locations across Alabama, California, Kansas, Maryland, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Multiple Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06980480's enrollment target sits among peer trials

183 118th of 438 higher than 321 of 438 other Multiple Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Multiple Myeloma 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 NCT06980480, the US trial registry maintained by the National Library of Medicine. NCT06980480 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.