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Study identifier: NCT05879757 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Real-world Usage of HyQvia in Multiple Myeloma Adults With Secondary Immunodeficiency

Condition: Multiple Myeloma · Secondary Immunodeficiency (SID)  ·  Sponsor: Takeda

PhaseN/A
Planned participants75
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

In this study, multiple myeloma participants with secondary immunodeficiency (SID) will be treated with HyQvia according to their clinic's standard practice. The study's main aim is to look into infusion parameters of HyQvia administration.

This description comes directly from the study's public registry record.

Talk to the study team

Takeda Contact  ·  +1-877-825-3327  ·  medinfoUS@takeda.com

Always discuss trial participation with your own doctor first.

Locations (27)

Instituto Privado de Investigaciones Clinicas de CordobaCórdoba, ArgentinaWithdrawn
Fakultni nemocnice PlzenPilsen, CzechiaRecruiting
Vseobecna fakultni NemocnicePrague, CzechiaNot Yet Recruiting
CHU Amiens - Hopital SudSalouël, Somme, FranceRecruiting
CHU Dijon - Hopital du BocageDijon, FranceNot Yet Recruiting
Hopital Prive du ConfluentNantes, FranceRecruiting
Hopital de la Source - CHR OrleansOrléans, FranceNot Yet Recruiting
CHU Bordeaux - Hopital Haut-LevequePessac, FranceNot Yet Recruiting
MHP-Muenchner HaematologiepraxisBerlin, GermanyNot Yet Recruiting
Alexandra General HospitalAthens, GreeceRecruiting
General Hospital of Thessaloniki "G. Papanikolaou"Thessaloniki, GreeceRecruiting
A.O.U.C Policlinico di BariBari, ItalyRecruiting

+ 15 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05879757